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Review

An Insight into Microbial Inoculants for Bioconversion of Waste Biomass into Sustainable “Bio-Organic” Fertilizers: A Bibliometric Analysis and Systematic Literature Review

by
Jennifer Michellin Kiruba N
* and
Agnieszka Saeid
*
Department of Engineering and Technology of Chemical Processes, Faculty of Chemistry, Wroclaw University Science and Technology, 50-373 Wroclaw, Poland
*
Authors to whom correspondence should be addressed.
Int. J. Mol. Sci. 2022, 23(21), 13049; https://doi.org/10.3390/ijms232113049
Submission received: 31 August 2022 / Revised: 19 October 2022 / Accepted: 24 October 2022 / Published: 27 October 2022
(This article belongs to the Special Issue The Role of Biostimulants in Stimulating Plant Productivity)

Abstract

:
The plant-microbe holobiont has garnered considerable attention in recent years, highlighting its importance as an ecological unit. Similarly, manipulation of the microbial entities involved in the rhizospheric microbiome for sustainable agriculture has also been in the limelight, generating several commercial bioformulations to enhance crop yield and pest resistance. These bioformulations were termed biofertilizers, with the consistent existence and evolution of different types. However, an emerging area of interest has recently focused on the application of these microorganisms for waste valorization and the production of “bio-organic” fertilizers as a result. In this study, we performed a bibliometric analysis and systematic review of the literature retrieved from Scopus and Web of Science to determine the type of microbial inoculants used for the bioconversion of waste into “bio-organic” fertilizers. The Bacillus, Acidothiobacillus species, cyanobacterial biomass species, Aspergillus sp. and Trichoderma sp. were identified to be consistently used for the recovery of nutrients and bioconversion of wastes used for the promotion of plant growth. Cyanobacterial strains were used predominantly for wastewater treatment, while Bacillus, Acidothiobacillus, and Aspergillus were used on a wide variety of wastes such as sawdust, agricultural waste, poultry bone meal, crustacean shell waste, food waste, and wastewater treatment plant (WWTP) sewage sludge ash. Several bioconversion strategies were observed such as submerged fermentation, solid-state fermentation, aerobic composting, granulation with microbiological activation, and biodegradation. Diverse groups of microorganisms (bacteria and fungi) with different enzymatic functionalities such as chitinolysis, lignocellulolytic, and proteolysis, in addition to their plant growth promoting properties being explored as a consortium for application as an inoculum waste bioconversion to fertilizers. Combining the efficiency of such functional and compatible microbial species for efficient bioconversion as well as higher plant growth and crop yield is an enticing opportunity for “bio-organic” fertilizer research.

1. Introduction

Numerous studies have reported that the overuse of conventionally used synthetic fertilizers contributes to the degradation of soil quality in most arable land and negatively impacts its biological community. Although the application of certain chemical fertilizers has improved agricultural yield in response to the increasing demand over the previous decades, now the question of sustainability arises, in the long run, amid decreasing resources and raw materials [1]. This brings about the need to deviate from the traditional linear model of biofertilizer production and adopt circular production from different types of waste-based resources. While the application of synthetic fertilizers since the 1950s has gone a long way in providing food security for many developing countries, they also have downsides due to their extensive overuse.
The inefficient and inappropriate use of chemical fertilizers has led to problems on multiple fronts such as soil quality degradation, groundwater contamination, loss of biodiversity, decrease in soil fertility, resistance development in pests, and acidification issues, among other potential agricultural-based non-point source pollution (NSP) [2,3,4]. On the other hand, several studies propose the replacement of chemical fertilizers with organic, bio-organic, and microbial fertilizers [5,6].

1.1. The Need for Bio- and Bio-Organic Fertilizers

Biofertilizers are generally defined as an organism-based composition of micronutrients and carbon substrates such as bacteria, cyanobacteria, fungi, and algae, that can nourish and enhance soil quality [7]. They also have the advantages of being cheap alternatives to synthetic fertilizers, improving crop quality, soil fertility, and food safety while all the while being sustainable. Most common and popular biofertilizers are green manures such as cyanobacterial amendments, bio-formulations of bacteria such as Azotobacter sp., Azospirillum sp., Trichoderma sp., and arbuscular mycorrhizal fungi (AMF) [8]. Apart from microbial “biofertilizers”, organic-based fertilizers are also commonly used by the farming community which includes composting residues such as vermicomposting, agricultural crop residues, and farmyard manure.
The current strategies used to produce biofertilizer bioformulation are the usage of carrier materials such as slurries, granules, powder, and liquid formulations for the dispersal of microbial inoculums targeting the appropriate part of the crop such as root, shoot, or flowers. Microbial inoculums in the form of lyophilisates (powders) or liquid broths (grown in media) are added to various carriers such as clay, peat, and sand, producing a granular or freeze-dried product for distribution [9,10]. The technology of inoculum development for microbial bio-formulations and their carrier substrates are discussed in detail in [11].

1.2. The Integration of Circular Economy (CE) in Bio-Organic Fertilizer Production

The burgeoning population with their ever-increasing demand for food and nutritional security substantiates the necessity of biofertilizer research. While in the early stages of biofertilizer research, the raw materials used for bio-formulations such as media supplementation for microbial and algal growth were produced as part of a linear economic model, currently, the production is required to be more sustainable. Various resources such as agro-industrial and municipal wastes are suitable secondary raw materials with appropriate physicochemical composition to be utilized for fertilizer production. According to the CE concept, agro-food industrial wastes and municipal solid waste residues have been extensively studied from the perspective of biorefineries to produce fuels, biochemicals, energy, and biomass. The valorization of waste biomass after pyrolysis or combustion to generate viable and sustainable biofertilizers is being actively pursued [7]. For sustainable use of natural resources used in the production of biofertilizers or organic-based fertilizers as well as to replace the use of chemical fertilizers, biomass generated from food, municipal, and agricultural wastes are processed using composting, aerobic and anaerobic digestion, combustion, pyrolysis and chemical hydrolysis among other technologies [12,13].

1.2.1. Waste Valorization

As discussed above, the enforcement of EU and UN SDG-based policies on circular economy (CE) have led to the development of waste-based biorefineries. This biorefinery concept works on the fundamental principle of waste valorization technologies. Valorization of the wastes considers various types of sources such as food waste, e-waste, agro-industrial wastes, municipal solid waste (MSW), construction and demolition (C&D) debris, medical wastes, textile, plastics and mining associated wastes, which in turn depends on the type of technology applied to convert the waste into a sustainable product such as biomass, biofuel, bioenergy and others [14,15]. A detailed discussion of three major technologies adopted in waste valorization pathways is provided in [16]. One of the pathways includes the search for technology that generates a fuel that not only replaces fossil fuels in terms of supply and demand but also produces less greenhouse gas emissions and carbon footprint. Using waste biomass to produce cleaner energy is one major path favored by environmental-friendly policies. Similarly, the other pathways of waste valorization focus on the biorefinery approach of producing bioplastics, biochemicals, solvents, and biomass from a circular supply chain of waste material using various valorization technologies such as microwave-assisted, pyrolysis, chemical extraction, separation, and isolation techniques, pyrolysis, and bioengineering approaches such as enzymatic, chemo-enzymatic, solid-state fermentation, bioreactor technology, and bioconversion strategy.

1.2.2. Bioconversion

Bioconversion is a biotechnological strategy for waste valorization that exploits the metabolic and enzymatic versatility of a microorganism to produce a sustainable bio-compound such as solvents (acetone), acids (lactic acid, citric acid), bioplastics, biofuels (biodiesel), and other value-added substances post the treatment of waste biomass from any industry through the process of fermentation, digestion or solubilization [17].
This strategy is being extensively applied to convert waste biomass into appropriately formulated biofertilizers. For instance, composting and anaerobic digestion (AD) processes are in effect bioconversion approaches that utilize the metabolic capacity of the thermophilic and decomposer microbial community present in the green manures and lignocellulosic material used in them. Often native and indigenous microbial communities present in a selective habitat possess a unique and specific assortment of enzymatic tools that co-metabolize different substrates (including recalcitrant pollutants) and biotransform metal species to bioavailable forms. However, these localized microbial communities are rather slow and non-optimal, and often require external stimulus through bioaugmentation or biostimulation. Likewise, several studies have tested the bioconversion efficiency of composting and AD processes with the addition of a microbial seed inoculum [18]. Presently, many studies have been conducted to assess the efficiency of microbial fermentation and bio-solubilization to convert other waste materials to fertilizers that specifically target NPK enrichment in soil or plants or produce plant biostimulant components such as humic substances, phytohormones, betaines and bioavailability of micronutrients [19].

1.2.3. Microbial Inoculants

Although microbial inoculants and inoculum technology have a long history in fertilizer and agricultural research, their roles in waste valorization technology for the bioconversion of waste biomass into high-value-added plant biostimulant products are of new and high interest. Bioconversion of secondary raw materials, such as agroindustrial wastes, that are rich in NPK and organic matter necessary for plant growth by the employment of target-specific microorganisms is an evolving field of research. Such a synergistic combination of waste biomass and plant-growth-stimulating microorganisms creates bioorganic fertilizers that reduce dependence on primary raw materials and synthetic fertilizers. They may alleviate issues such as the dispersal of antibiotic resistance and the persistence of recalcitrant residues in current compost and AD-based fertilizers, reducing soil pollution and enhancing crop yield, and soil health [20]. In recent years, the addition or supplementation of microbial inoculants to AD or composting processes have been tested to increase the efficiency of the biorefinery process. Herein, we would like to enlist the research undertaken in the field of bioconversion employed to convert waste biomass into “bio-organic” fertilizer with the aid of substrate-specific microbial inoculant.
Therefore, this study attempts to conduct a bibliometric analysis of biofertilizer research trends during 2012–2021 (the last five years) and a systematic literature review of relevant articles during the same period to determine the microbial inoculants of interest that have been employed for bioconversion of wastes to bio-organic fertilizers.

2. Methods

2.1. Objectives

The study attempts to track the research trends in biofertilizers in the last five (2017–2021) years, through a bibliometric analysis and systematic literature review of research articles retrieved through specific search strategies from the SCOPUS and Web of Science database.

2.2. Search Analysis in Scopus

Searches were conducted in the Scopus and Web of Science database for bibliometric analysis and systematic literature review. The search results were retrieved from the Scopus database using a combination of keywords such as “plant growth”, “fertilizer”, “bioconversion”, “biofertilizers”, “bioinoculant”, “fungi”, “bacteria”, and “waste”. The detailed search strategy is provided in Table 1. The data of the number of articles published by different categories such as journals, year, and country were exported and analyzed.

2.3. Bibliometric Analysis by VOSviewer

The bibliographic information of the search results was exported in csv format and analyzed using VOSviewer 4.0 by keywords, co-occurrence patterns of terms, and citation [21]. The bibliographic data was preprocessed during VOSviewer analysis by removing keywords used in the search strategy such as “plant growth”, “fertilizer”, “bioconversion”, “biofertilizers”, “bioinoculant”, “fungi”, “bacteria”, and “waste” to avoid bias in the results. Moreover, during the analysis of index keywords used by the journals, terms such as “priority”, “nonhuman”, and “article” were also cleaned up. Once biased keywords used in the search and retrieval were removed, the weights and scores were set to total link strength and averaged normalized citations, respectively.

2.4. Systematic Literature Review

2.4.1. Scope and Definitions

The research question of the study was framed based on PICO [22] and guided by the PRISMA methodology [23]. This review was devised to address the trends in biofertilizer research undertaken during the last five years. The PICO framework is tabulated in Table 2.

2.4.2. Data Retrieval for SLR

The articles were retrieved from the SCOPUS and Web of Science database and were restricted to the last five years (2017–2021). Keywords such as “plant growth”, “fertilizer”, “bioconversion”, “biofertilizers”, “bioinoculant”, “fungi”, “bacteria”, and “waste” were used to search and retrieve relevant articles from the database into csv format for further analysis. Articles published in English alone were included in the search. Inclusion and exclusion criteria are tabulated in Table 3 and Figure 1. Based on the inclusion and exclusion criteria, screening of articles was carried out after duplicates were removed using MS Excel. The detailed search strategy is presented in Table 1. Thematic analysis of the final list of articles was performed to allocate them into different categories of research trends (Figure 2). A table of evidence (ToE) matrix was constructed from the relevant articles for further inference and interpretation.

3. Results

3.1. Analysis of Search Results from Scopus and Web of Science

Based on the data exported from the Scopus database using a preliminary search of the keyword “biofertilizer” during the years 2017–2022, the geographical distribution of the research was plotted and indicated in Figure 3. As observed on the map, countries such as India, China, and South American countries seem to produce the most research in the field of biofertilizers. A comparison between the number of research articles produced per keyword can be seen in Figure 4.

3.2. Bibliometric Analysis by VOSviewer

VOSviewer was used to allocate emerging themes of research and research trends of the past five years through analysis of bibliometric data. Figure 5 represents the co-occurrence mapping of author keywords by the full counting method through overlay visualization. The minimum co-occurrence of the author keywords in the research articles was set to 119 to identify the top 100 major keywords from more than 21,600 author and index keywords retrieved from multiple search strategies. These major keywords present a rather clear picture of the current directions of research in the field of bioorganic fertilizer production. A stark distinction exists between research associated with bioorganic fertilizer production strategies such as composting, anerobic digestion, biodegradation of wastes (manure), plant growth promotion abilities of microbial inoculants (biofertilizers), bioremediation, phytoremediation, and wastewater treatment. The identification of relevant microbial community appears to be at the center of all the connected themes.
Similarly, Figure 6 presents the plot of the co-occurrence map based on textual data provided in the title and abstracts of the research articles used in the study. Filtering of terms by binary counting, indicating their presence or absence in a research article and setting the minimum number of occurrences to 85, resulted in 100 relevant terms out of 69,247, based on 60% relevance. Co-occurrence mapping of the textual data also revealed three distinct groups of research interest, namely plant growth enhancement, the composition of microbial communities (such as diversity, structure, and succession) in biodigestion processes, and waste treatment strategies. An enormous volume of research has been generated that explores the plant growth promoting the potential of microbial inoculants as biofertilizers based on their ability to produce indole acetic acid (IAA), siderophores, hydrogen cyanide (HCN), ACC deaminase, phytohormone production, salt tolerance, and micronutrient solubilization. Conversion of secondary raw materials to value added products and removal of organic pollutants through waste treatment are some basic waste management techniques often prospected. Similarly, deciphering composition of the microbial communities provides insight into the structure and diversity of the microbial species such as Proteobacteria, Acidobacteria, Bacteroidetes, methanogens, and their significant functional roles in composting and anaerobic digestion processes.
The terms in the three groups could be classified as given in Table 4.
Figure 7 is a representation of the co-authorship mapping between countries of studies included in this analysis, weighted by total link strength between countries and scored by average normalized citations. Filtered by setting the minimum number of documents as 16 per country, the top 50 countries met the relevant thresholds out of 188. It can be observed that the United Kingdom, Australia, Sweden, Switzerland, Denmark, Netherlands, Singapore and Hong Kong produce some of the heavily cited research in fertilizer research, though not voluminous (yellow in map). However, countries such as India, China, Pakistan and Brazil appear closely associated with co-authoring and collaborating with fertilizer research, producing quite a large number of research articles.
Journals such as Bioresource technology, Journal of Hazardous Materials, Science of Total Environment, and Environmental pollution are some of the most preferred journals and well cited among authors (Figure 8).

3.3. Systematic Literature Review

A literature search carried out in the Scopus and Web of Science database using the keywords “biofertilizers”, “waste” and “bacteria” yielded 6136 research articles. After data cleaning of duplicates and ineligible entries, 3567 articles remained. When the exclusion and inclusion criteria were applied to relevant articles based on the title and abstract screening, 3489 were excluded and were unable to retrieve two of them. A final list of 74 research articles was systematically analyzed and a table of evidence (ToE) was constructed and is provided in Table 5 and Table 6

3.3.1. Microbial Inoculants Used for Bioconversion

More than 55% of the studies (n = 44) used microbial monoculture for bioconversion of wastes, whereas nearly 20% and 14% (n = 16 and 11) used microbial consortia and dual cultures, respectively. Similarly, bacterial cultures were used in nearly 68% (n = 58) of the studies, among which five of them used actinomycetes alone and eight of them utilized cyanobacterial biomass for nutrient recovery from wastes. Eighteen studies included purely fungal bioconversion and three studies alone used mixed cultures of fungi with bacteria. Bacillus sp. was among the most used bacterial isolates for all types of bioconversions of wastes ranging from dairy wastewater, potash, sewage sludge ash, rock phosphates, bone meal, manure and feather wastes [24,25,26,27,28,29,30]. Secondary to Bacillus, cyanobacterial species such as Scenedesmus, Chlorella, and Anabaena, (n = 8) followed by bacterial species Acidithiobacillus (n = 3) and fungal species Aspergillus sp. (n = 7) were used.
Among the consortia used for bioconversion, different types of wastes such as sawdust, chicken litter, wastewater from municipal, food and dairy industry, feather waste from the poultry industry, agricultural residues and petroleum sludge were tried and tested (Table 6). Though studies abound on the plant growth promoting efficiency of Trichoderma biofertilizers [31], commercial yet controversial “Effective Microorganisms” (EM) inoculants [32], and microalgal biomass [33], reports on their usage for waste valorisation are not numerous.
The exhaustive list of microbial inoculants used in bioconversion studies in the last five years (2017–2021), the bioconversion strategy adopted in each study, the mode of application of digestate, and the type of plant growth test (plot/pot/germination) have been compiled and presented in Table 6.
However, the identity of the microbial agent (MA-1) mentioned in [52], used for the composting of a combination of wastes consisting of spent coffee grounds, poultry manure and biochar, was undetermined. Furthermore, one of the studies determined the biodegradation of sludge produced by the petroleum industry by the application of Effective Microorganisms (EM) bokashi under anaerobic conditions. The exact microbial composition of EM bokashi used in this study was also undetermined [40].

3.3.2. Bioconversion Raw Materials and Strategies

Three main bioconversion strategies were commonly observed to be adopted in these studies, and they are aerobic composting, solid-state fermentation, and submerged (liquid) fermentation. A team of researchers from Poland utilized carrier-based bioformulation enriched with Bacillus megaterium and Acidithiobacillus ferrooxidans in granular form to study the phosphate solubilization and plant growth promoting the potential of a waste material composition of wastewater treatment plant (WWTP) ash, also referred to as sewage sludge ash, spent mushroom substrate (SMS) and slaughterhouse waste (bone meal and dried animal blood) [25,30,68,101].
Moreover, all wastewater nutrient recovery and bioconversion-to-biomass studies were undertaken using micro-algal-based biorefinery approaches. Diverse types of wastewaters from sources, such as breweries, toilet (black water), dairy and paddy-soaked rice mill water, were used to cultivate microalgal species such as Chlorella sorokiniana, Scenedesmus obliquus (ACOI 204/07), Chlorella sp., Dictyosphaerium sp., Monoraphidium sp., Neochloris sp., Scenedesmus sp., Chlorella pyrenoidosa, and Scenedesmus sp. (Table 6). Only one study attempted to utilize a cyanobacterial concoction consisting of Fischerella muscicola, Anabaena variabilis, Aulosira fertilissima and Tolypothrix tenuis for bio-manure production from chili crop waste [37].
A single study reported the use of mesophilic digester (anaerobic digestion) for the production of biofertilizer from a waste composition containing sardine waste, potato peels and poultry waste after the inoculation of the fungus Aspergillus niger and yeast Saccharomyces cerevisiae [61]. However, in a unique investigation by Feng et al. [53], bioremediation of phthalate acid esters (PAEs)-contaminated soil was achieved by the addition of a bio-organic fertilizer which was synthesized by the inoculation of Bacillus megaterium strains in the composting of sewage sludge and agricultural waste.
Seven studies focused on the degradation of keratin-rich chicken feather waste using both fungal and bacterial monocultures of Alternaria tenuissima, Bacillus cereus PKID1 and Bacillus pumilus JYL under submerged fermentation conditions, while ten studies reported the plant growth efficiency of waste digested with phosphate solubilizing microorganisms (Table 3). Biodegradation-based treatment of wastes containing higher ratios of fatty acid residues such as petroleum and kitchen oil were carried out in the presence of EM bokashi consortia and Pseudomonas aeruginosa PA-3 [40,71].
Corynebacterium glutamicum, a Gram-positive bacterium mostly used in the industrial production of amino acids, has been applied by a research team at the Federal University of Parana in Brazil for the fermentation-based production of biofertilizers from sugarcane molasses [57,87].

3.3.3. Plant Growth Tests and Mode of Application

On the other hand, nearly 50% of the studies adopted pot (n = 38) and plot tests (n = 25) to determine the efficiency of their biofertilizer formulation. Only three studies determined their plant growth promoting the potential of their product using seedling germination tests. More than 70% of the studies (n = 55) employed their product as a soil amendment for their plant growth tests.
Foliar application was tested in three studies where the fermentate obtained from sugarcane molasses by Corynebacterium glutamicum was tested on potato and Brassica campestris var. Pekinensis and lignin waste fermented by phosphate solubilizing mixed culture of fungal strain Meyerozyma guilliermondii and bacterial isolate Providencia rettgeri was tested on cowpea plants [57,87,97]. Soil irrigation using the fermented wastes of dairy wastewater and kitchen oil waste was applied on cabbage and mung bean plants in plot tests. Feng et al. [53] employed a modified strategy of soil amendment by spiking the pot tests with pollutants at appropriate concentrations before plant growth tests.

4. Discussion

Bioconversion studies are being conducted at much higher volumes than biofertilizer research, whereas waste valorization studies have gained momentum only in the last decade (Figure 2). However, the volume of biofertilizer-associated research is comparatively lower compared to waste valorization and bioconversion research. Moreover, the graph indicates that biofertilizer and waste valorization research have been comparatively recent when compared to bioconversion studies. It can also be observed that there is a wide gap between the research focussing on “plant growth” promoting microorganisms and their application for waste bioconversion studies.
During the systematic literature review, the authors observed that the predominant themes among the search results were associated with anaerobic digestion (AD), vermicomposting, algal nutrient recovery from wastewater, and biofertilizer. It seems necessary to highlight the relevance of anaerobic digestion (AD), composting (including vermicomposting), and nutrient recovery studies from wastewater treatment plants (WWTP) in bioconversion of waste biomass. Other minor themes that were explored in literature survey were production technology (pre-treatment techniques) of bio-based fertilizers, testing of the impact of microbial biofertilizers (bioinoculants and biostimulants) in the specific host plant, carriers used for biofertilizer formulation and study of microbial communities after application of biofertilizers.

4.1. Current Strategies of Fertilizer Production Using Bioconversion

4.1.1. Composting and Vermicomposting

Composting is essentially a traditional system used for the aerobic and thermophilic digestion of organic waste such as leaf litter and cow dung, converting both solid and liquid waste to humus which is essential for plant growth. Several strategies such as rotary drum, windrow, and aerated static piling where n number of factors can be adjusted such as type of substrate, substrate capacity, duration of composting, and quality of end-product [102]. Composting by the employment of earthworms (Eisenia foetida, Eudrilus eugeniae, and Perionyx excavatus), vermicomposting, also enhanced the quality of composted organic wastes. Vermicomposting has been noted to enhance the nutrient quality of the compost, as well as removal of potential pollutants through the aid of the invertebrate’s digestive system. [103]. However, the system comes with its own set of disadvantages, such as detection of pathogens in the compost, low micronutrient and humus content, long duration of the complete process and considerable generation of odour. In addition to design of appropriate composter, supplementing the compost waste materials with functional microbial inoculum to increase the compost quality has also been assessed in several studies [104].
In a study by [105] wood-rot fungi strains Lasiodiplodia sp. F1, Verticillium sp., and Trametes versicolor were observed to remove Tiamulin, a common antibiotic found in compost, from swine manure. A strain of Thermus sp. was isolated from pharmaceutical sludge with the potential for biodegradation of antibiotic ciprofloxacin from swine manure compost, where it is a common contaminant [106]. Bioaugmentation of functional microbes belonging to two different groups (PGPB and plant pathogen-suppressing bacteria) to a composting of spent coffee grounds (SCGs), rice bran, and biochar produced a significant increase in germination index and reduction in disease incidence [89]. Similarly, composting of palm oil empty bunches and sugarcane biomass in the presence of lignocellulolytic consortia of bacterial and fungal strains resulted in a decrease of recalcitrant cellulose and lignin content, as well as a C:N ratio [107].
Succession of different microbial communities has also been observed to be correlated to the composition of waste materials in the compost. Nakasaki et al. [108] identified the dominance of Bacillales taxa throughout the composting of organic-only waste, and the presence of Symbiobacterium at the last phase of composting. When composting of swine manure was amended with coconut shell biochar, the dynamics of the bacterial community diverged to include keratin degrading Firmicutes and Actinobacteria, to the already dominant Bacilli species [109]. This hints at the premise that supplementing substrate-specific microbial inoculum can enhance compost quality, nutrient content, and plant growth as a result.

4.1.2. Anaerobic Co-Digestion (AcoD) of Waste

Anaerobic digestion is one of the key mechanisms through which organic matter (or wastes) is converted to fuels such as biogas and its digestates as organic fertilizers. The digestates have exhibited quite an agronomic potential [110]. AD digestates have been produced from different types of biomasses and tested across diverse types of crops, wherein they have been proven to affect a significant increase in plant growth. Jamison et al. [101] tested the efficacy of a combination of digestates from two wastes such as food waste, and lignocellulosic biomass on the growth of Brassica juncea (Kai Choy). It was found to significantly increase the nitrogen use efficiency of plants, plant biomass, and root length. However, digestates from olive mill wastewater, domestic wastewater, and cow dung were found to induce phytotoxicity [111]. A similar study by [112] used combinations of cattle manure, cheese whey, and pig manure to determine their agronomic suitability. The study revealed that the digestate had appropriate concentrations of NPK to be utilized as fertilizer but was unstable for long-term storage and carried fecal pathogens that can be transmitted to the soil. The study also recommended a suitable post-treatment of the digestates prior to field application.
The process of anaerobic digestion often involves the addition of a seed microbial inoculum that is dependent on the type of waste (or substrate) that needs to be digested, and the inherent microbial community that drives the whole process such as methanogens and acetogens. Most often, the inoculum is prepared from an already existing digester depending on the physicochemical factors that determine AD such as pH, temperature, C:N ratio, volatile fatty acids (VFA), and others. When anaerobic rumen fungi were added to anaerobic digestion of cattle manure, it was found to increase the biogas yield [113]. Similarly, the addition of livestock manure to anaerobic co-digestion of palm oil mill effluent and brewer’s spent grain was found to enhance the plant growth promoting bacteria (PGPB) community and micronutrient levels (K, P, Ca, Mg, S, N). While pretreatment of biomass is often necessitated, recent research has been propagated to turn toward microbial pretreatment for enhancement of the AD process.
Among the AD studies, the primary focus of the research was on the prevalence of ARGs, coliform, pathogens, different types of waste digestion, and life cycle assessment (LCA), including several exhaustive reviews on AD and composting. For instance, Golovko et al. [114] estimated the risk associated with the widespread use of anaerobic digestates from biogas plants as fertilizers by characterizing the number of heavy metals, food-borne pathogens, antibiotic-resistant bacteria, antibiotics, pesticides, and other chemicals of emerging concern (CECs). A similar study by Södergren et al. [115] assessed the microbiological safety of using the liquid digestate produced from the biogas plant for the hydroponic cultivation of vegetables.

4.1.3. Nutrient Recovery and Wastewater Treatment by Microalgae

An important sustainable technology with considerable contribution to the circular economy is converting wastewater streams from various sources such as municipal wastewater and industrial effluents to recover nutrients with application as fertilisers. Microalgae, also known as cyanobacteria, are photoautotrophic microorganisms that are capable of fixing carbon dioxide to organic biomass. They are resilient to grow in diverse environments and can generate large amounts of biomass rich in physicochemical composition of lipids and proteins from using the nutrients and micronutrients available in the wastewaters. The available technology including the design of the photobioreactor, downstream processing, large-scale implementation and its economic feasibility has been extensively discussed by [116,117].
To add more value to the end-products, an algal consortium consisting of Chlorella sp. and Scenedesmus sp. grown in wastewater was used for lipid production. When the residual deoiled biomass was supplemented as organic fertilizers for the growth of Solanum lycopersicum, it was found to enhance plant biomass and tomato yield [91]. Similarly, deoiled biomass of a monoculture of Scenedesmus sp. provided 100% nitrogen required for rice crop, and significantly increased grain weight, panicle weight, and plant dry weight [79]. Microalgae is a powerful tool for the bioconversion of wastewater into biofertilizers and fits tightly into the biorefinery approach [118,119].

4.1.4. Bio-Organic Fertilizers

Several studies reveal that treatment of soil or plant growth with co-inoculation of microbial fertilizer and soil amendments enhances the availability of NPK, micro-, and macronutrients to the plants. The use of these inoculants for the targeted digestion of waste biomass for the elution of NPK and other plant-growth promoting factors, and its application as a “bioorganic fertilizer”, is a considerable bioconversion technology. Depending on the biochemical composition of the waste biomass, a suitable microbial inoculant or consortia can be applied for efficient bioconversion or solubilization. Microbial inoculants used in the digestion of substrates and tested for its capacity to promote plant growth have been enlisted in Table 3. Meanwhile, the trends in the research are predominantly associated with the application of microbial biofertilizers, which can be classified into five main types, and have been extensively reviewed by several authors:
  • plant growth promoting rhizobacteria or bacteria and fungi (PGPR, PGPB and PGPF) [120,121,122];
  • phosphate and potassium solubilizing bacteria (PSB and KSB) [123,124];
  • mycorrhizal fungi (AMF) [125];
  • Nitrogen-fixing bacteria (NFB) [126,127];
  • Non-mycorrhizal fungi and endophytic fungi [122,128].

4.2. Mechanism of Microbial Bioconversion

4.2.1. Microbial Fermentation

It is well-understood that microorganisms require a constant supply of carbon and nitrogen feedstock for their survival, and possess a large array of tools such as biochemical pathways, production of organic acids, and enzymes to utilise them. Agro-industrial wastes, and other types of wastes, make an appropriate nutrient medium for microbial fermentation. The term microbial “fermentation” indicates anaerobic catabolism of diverse substrates (e.g., sugars) to produce ATP as their source of energy. The catabolism is not complete oxidation of substrate to carbon dioxide, but rather partial breakdown to organic acids such as lactic acid, acetic acid and ethanol [129]. Agro-industrial wastes and municipal solid wastes are often rich sources of micronutrients (NPK) and protein content that enhance plant growth in nutrient-deficient environments.
While microbial fermentation in bioreactors is employed by several industries in food, and pharmaceutical industries for the production of metabolites, the mode of fermentation can be classified into two: submerged fermentation (SmF) and solid-state fermentation (SSF). Submerged fermentation indicates the process of microbial catabolism of substrates in the presence of water or water-based nutrient media, mostly in bioreactors where parameters such as pH and aeration are controlled [130]. Whereas solid-state fermentation, as the name indicates, is carried out using substrates which require or have low water content, produce high concentration of products, and have simpler downstream processing. Both methods have their advantages and pitfalls in their use for biomass conversion, which are discussed extensively by [131]. Buntic et al. [132] compares these two modes for the fermentation efficiency of cellulose production from waste tobacco using Sinorhizobium meliloti strain 224 as an inoculum. Several factors such as the type of biomass (lignocellulosic, MSW), the type of strain (PGPB, PSB, AMF), base of bioformulation (liquid, solid), and the type of scaling-up must be optimised to choose the suitable mode of fermentation [133].

4.2.2. Microbial Lignocellulolysis, Keratinolysis, and Chitinolysis

Agroindustrial and seafood wastes are rich sources of cellulose, lignin, hemicellulose, chitin, and pectin which are recalcitrant polysaccharides that can be decomposed into pentoses and hexoses, which are nutrients for microorganisms. Microorganisms are bio-factories that produce an array of cell wall degrading enzymes (CDWE) such as glycosidase, amidase, β-glucosidases, ligninases (laccases, Mn-peroxidases, polyphenol-oxidases), pectinases, xylanases, mannanases, cellulolytic oxidases, and cellulases [134,135,136].
Green waste fraction of MSW composted using ligninolytic and cellulolytic fungi was amended to soil for the growth of red chillies and found to enhance plant biomass and its chlorophyll content [67]. Fruit and vegetable wastes (FVW) co-digested in a two-phased manner with slaughterhouse wastewater (SWW) in the presence of Trichoderma reesei revealed reduction in its lignin and cellulose content, and high C:N ratio required in biofertilizers [137]. Palm oil empty bunches and chopped sugarcane biomass with a high ratio of lignin and cellulose were heavily reduced upon the inoculation and composting in the presence of up to 4% cellulolytic and ligninolytic bacteria and fungi [107]. Sweet sorghum bagasse (SSB) was subjected to fungal pretreatment by Coriolus versicolor through solid-state fermentation and was found to be an efficient pretreatment method which made the substrates more vulnerable and accessible to prolonged enzymatic saccharification [138]. Biotransformation of lignocellulosic biomass (LCB) and low-density oxodegradable polyethylene (LDPEoxo) through co-digestion using Pleurotus ostreatus as inoculum, producing a “bio-organic” (BoF) fertilizer that enhanced plant growth of Allium cepa. It was correlated to the synergistic effect of hydrolytic enzymes and oxidative enzymes (ligninases, cellulases and hemicellulases), via co-metabolism [139]. Silva et al. [140] provides a detailed insight on how CDWE can be manipulated through enzyme engineering to encompass lignocellulosic biomass into the biorefinery concept.
Similar to agro-industrial wastes, seafood processing wastes such as crustacean shell waste and shrimp waste contain high ratios of chitin, a polysaccharide with nitrogen functional group, micronutrients in the form of calcium carbonates, phosphates and proteins. Microbial bioconversion of shrimp and crab shell wastes was attempted using a chitinase-producing Alcaligenes faecalis SK10 strain and assessed for its potential as fertiliser on the growth of growth of Pisum sativum and Cicer arietinum. When compared to fertiliser doses of raw chitin, the fermented hydrolysate showed performances on par for several parameters such as micronutrient content (NPK) of soil, plant growth, and chlorophyll content [82]. A marine bacterium Exiguobacterium antarcticum DW2 was found to produce a cold-temperature chitinase that hydrolyzes chitin to bioactive polysaccharides [141]. A chitinase gene was identified in the biosynthetic gene cluster of an endophytic Bacillus subtilis Dcl1 that isolated from the dried rhizome of Curcuma longa, which also contained several plant promoting factors such as drought tolerance and IAA production [142]. Strains of chitinolytic Streptomyces were isolated from lobster processing wastes exhibited demineralization, and deproteinization of lobster shells in addition to inducing disease resistance against Botrytis cinerea in Arabidopsis [66]. Moreover, these microbial strains that produce chitinase have an advantage of carrying host–defense systems for plant growth against pests [143].
On the other hand, feather waste from the poultry processing industry is one of the richest sources of protein, available in the form of keratin. However, due to the recalcitrant and insoluble structure of keratin, microbial isolates produce specialised serine metalloproteases that enable complete catabolism. Kocuria rhizophila p3-3 isolated from chicken was utilized for the valorisation of chicken feathers, and degraded them up to 52% in just 4 days at room temperature [48]. Strains Trichoderma asperellum and Trichoderma atroviride were cultivated on chicken feathers and sheep wool produced microbial formulations that had plant biostimulant properties and contained protein hydrolysates and metabolites that impacted seed germination, along with crop productivity [144]. Tamreihao et al. [145] provides a detailed overview of the agronomic potential of feather valorization and feather-derived keratin hydrolysates in the adoption of circular economy.

4.2.3. Microbial Micronutrient Solubilization—Phosphorus

Phosphorus is an essential micronutrient for plant growth, and natural resources for phosphorus fertiliser production currently used are two types of raw materials called sedimentary rock (phosphorite) and volcanic sediment (apatite). However, there is a need to incorporate the concept of circular economy and biorefinery into production of NPK fertilizers, as we might reach peak phosphorus soon [146]. Several types of wastes including agricultural residues and wastewater sludge contain different forms of phosphorus which are often in unavailable forms to plants. In addition, recovery of these phosphates for application in plant growth through industrial means can be expensive and defeats the purpose of a circular economy.
However, phosphate solubilizing microorganisms possess the ability to enhance the release of phosphates from wastes through production of acids such as oxalic acids, and enzymes such as phosphatases and phytases. A study by [147] tested the efficiency of Bacillus megaterium, Bacillus subtilis, and Bacillus cereus isolates to solubilise phosphates from three different waste materials (poultry bones, fish bones and ash). Production of acetic, gluconic, propionic, lactic and succinic acids were revealed to play important roles in phosphate solubilization, and fish bones provided the highest concentration of released phosphates. In a similar study, a thermotolerant consortium of Streptomyces was added as inoculum to the composting of organic wastes and was noted to solubilize up to 50 µg/mL from the wastes [148]. When a consortium of four strains of Penicillium bilaiae, Penicillium aculeatum and Aspergillus niger were added to a combination of sewage sludge ashes and biochar, it was observed to increase the P availability in spring wheat [86].
More than 325 mg/L of phosphate was solubilized from hydroxyapatite produced from Coptodon rendalli (tilapia) fish scales by the strain Acidovorax oryzae ZS 1–7 [149]. Production of acid and alkaline phosphatase enzymes led to the increase in acid levels and available P when Herbaspirillum seropedicae was inoculated into a compost made up of poultry litter and crushed grass (Pennisetum purpureum Schumach) [150]. Compost made up of by-products of sugarcane such as filter cake and ash, inoculated with phosphate solubilising Pseudomonas aeruginosa PSBR12 and Bacillus sp. BACBR01 improved the supply of available P to 150 kg ha−1, increased sugarcane yield, acid phosphatase and β-glucosidase activity [73]. The use of phosphatases, phytases, and phosphate solubilizing microorganisms to solubilize unavailable P from agroindustrial wastes can reduce our dependence on finite P resources [83,151].
Similar to P, other micronutrient solubilizing microbes (MSMs) such as zinc (Zn), nickel (Ni), manganese (Mn), magnesium (Mg), potassium (K), copper (Cu) and selenium (Se) have been exploited as microbial biofertilizers and carry applicable advantages as “bio-organic” fertilizers for mineral-deficient soils and waste valorisation, synergistically [152,153].

4.2.4. EPS Production

Bacteria are usually found as communities attached to a surface rather than as planktonic cells floating in a nutrient medium and secrete an exopolymeric matrix that contains proteins, nucleic acids, and exopolysaccharides (EPS), which is often visible as a slimy layer. Seneviratne et al. [154] observed that, when fungal strains were incorporated with N2-fixing rhizobial strains, they formed fungal–rhizobial biofilms (FRBs) that had potential in biocontrol and fertilisation of nitrogen deficient soils. Rathnathilaka et al. [155] determined that supplementation of BFBF to conventional large scale paddy cultivation increased crop yield, soil micronutrients, and influenced microbial communities. Similarly, bacteria can also be utilised to produce exopolysaccharides (EPS), a major component of biofilms from wastes. Halomonas strains were used to produce EPS rich in galactose from cheese whey wastes [156]. EPS production was evaluated by inoculation of lactic acid bacteria (LAB) Leuconostoc mesenteroides WiKim32 in spent media wastewater (SMW) derived from kimchi fermentation and exhibited antioxidant activity [157]. Solid-state fermentation of cane bagasse and broadbean seed capsule by Kosakonia cowanii LT-1 yield maximum yield of EPS, promoted germination index, and growth vigour in Zea mays [55]. Exopolysaccharides and biofilm biofertilizer (BFBF) produced by plant growth promoting bacteria (PGPB) have the potential to act as a biocontrol agent and protect plants against abiotic stress such as heavy metal contamination or drought [158].

4.2.5. PAE and LCT Biodegradation

Phthalate esters (PAEs) are contaminants of emerging concern (CEC) in agricultural soils of several countries and are quite often correlated with improper garbage disposal resulting in the leaching of Di(2-ethylhexyl) phthalate (DEHP), Di-n-butyl phthalate (DnBP) and Diisobutyl phthalate (DiBP) into water sources of irrigation [153,159,160,161,162,163,164]. Feng et al. [53] adopted the incorporation of a “bio-organic” fertilizer strategy to address this concern. A mixture of sewage sludge and agroindustrial residues was concocted with the addition of two bacterial strains of B. megaterium (YJB3, YLYP1) that had PAE-degrading as well as phosphate solubilizing abilities. A significant decrease in translocated concentration of PAEs in plants (chinese flowering cabbage) cultivated in contaminated soils and an increase in crop yield was observed. Similarly, application of organic fertilizer to plastic-shed soil was found to significantly enhance Planifilum, Geobacillus, and Thermaerobacter species, and correlated with the degradation of oligomeric dibutyl phthalate (DBP) to monomeric monohexyl phthalate (MEHP) and mono-n-butyl ester (MBP) [162].
There has been extensive research in the biodegradation of hydrocarbons including oil wastes generated from the food industry [160,161]. However, the potential of waste kitchen oil, having higher ratios of long chain triglycerides (LCT), as an ideal feedstock for biodiesel production through enzymatic transesterification, has been much explored, Marchetti et al. [159] identifies that the efficiency of kitchen waste oil degradation is enhanced by the co-digestion of pig slurry in anaerobic digestion. However, in a unique study, the bacterial strain Pseudomonas aeruginosa PA-3 was used to break down kitchen waste oil into shorter chain fatty acids, and the by-products were revealed to enhance plant growth and biomass in cabbage [71].

4.3. Microbial Community Analysis

The advent of culture-independent techniques, such as high throughput sequencing and metagenomics, has been used to understand the dynamics of the microbial communities in response to the concentration of different substrates in the available waste streams.
Microbial community analysis using amplicon sequencing and metagenomic approaches was also quite common, especially in anammox-associated studies [165,166]. A consistent amount of research was also focused on the remediation of metal-contaminated soils using microbial strains, plants (phytoremediation), or a combination of both. High-throughput sequencing was employed to determine the changes in the microbial community prior to and post vegetation on zinc (Zn) smelting waste slag [167]. Similarly, the effect of inoculating Streptomyces griseorubens JSD-1 on the co-composting of rice straw and swine manure was found to significantly change the microbial biomarkers to the Bacteroidetes genera, which positively correlated with an increase in plant-available micronutrients NPK [168]. In a significant study by Jiang et al. [169], high-throughput amplicon sequencing of the 16S rRNA gene isolated from the co-digested pig manure and food wastes revealed that a suitable inoculum can drive the microbial dynamics and community in favour or against the digestion more than the physicochemical composition of the waste substrate.

4.4. Nomenclature

It is also important to note that several authors referred to the anaerobic digestates as “biofertilizers”, though the standard definition of the term “biofertilizers’’ often denotes the use of biologically active preparations that contain beneficial microorganisms that enhance plant growth and yield. Similar nomenclature can be seen in [170,171,172,173] and many more. Similarly, the term “organic fertilizer” is often used to indicate the production of a sustainable fertilizer from by-products of agriculture, and pastoral farming, such as manure, litter, and poultry droppings by means of composting or anaerobic digestion [174]. However, due to the growing understanding of the microbial community’s role in converting waste into plant available nutrients, a grey area arises in the usage of varying terminology. Since the liquid or solid digestates from anaerobic digesters or composters often contain a diversity of microorganisms in addition to organic, plant essential nutrients, the question of it being a “biofertilizer” or “organic fertilizer” is debatable. However, this necessitates the reinstatement of proper terminology for microbial inoculants used for the sole purpose of plant growth, such as “microbial biofertilizer.
It is necessary to highlight the significance of nomenclature applied in a significant number of research papers evaluated in this study. Though the term “biofertilizer” has been traditionally associated with the application of microbial inoculum or formulation for enhancing plant growth and yield, it has been observed that the term has also been applied to indicate “bio-based” or organic fertilizers. As per the literature, it is observed that fertilizers made from composting, AD, manure, and other waste digestates are also termed biofertilizers when the correct terminology indicates the use of organic fertilizers or bio-organic fertilizers [34]. Here, the scenario indicates a lack of awareness of term differentiation between microbial biofertilizers, denoting the use of fungi, protozoa, archaea, and bacteria for plant growth promotion, biofertilizers that indicate the use of other living organisms for plant growth, followed by organic or bio-organic fertilizers that stipulate the application of manure, compost or other waste-based plant growth promoting material in agriculture.
Here, the authors would like to highlight four different fertilizer products associated with the terminology “biofertilizers” along with their mechanisms
(a)
Microbial fertilizers such as bio-inoculation of plant-growth-promoting bacteria (PGPB) and arbuscular mycorrhiza (AM), biocontrol microorganisms (bioorganic fertilizers);
(b)
Organic fertilizers which are made from composting, AD, manure, and other waste digestates;
(c)
Biofertilizers made from agro-industrial, organic wastes (BFW) by the application of phosphate- and potassium- solubilizing, keratinase-digested, bacteria and fungi;
(d)
Combination biofertilizers.
It can be summarised that production strategies of biofertilizers have been approached in three different modes, microbial biofertilizers, biofertilizers from waste processed by composting or anaerobic digestion, and biofertilizers produced from wastes by the effect of microorganisms through bioconversion. Lacunae in other aspects of biofertilizer research such as carriers used for inoculant stability and different modes of inoculation like seed immersion, root inoculation, and foliar spray have also been noted. The usage of digestates and processed wastes from anaerobic digestion (AD) and composting as organic fertilizers, often wrongly termed biofertilizers, are extensively studied in comparison to microbial inoculant studies [175,176,177].

4.5. Mode of Valorized Biomass Supplementation

Various modes of fertilizer application have been explored by several researchers, and co-inoculation of microorganisms along with valorised biomass appears to be a predominant strategy. In contrast to the biorefinery approach of valorizing waste through the addition of substrate-specific microbial inoculum, microbial strains or consortia were supplemented along with organic fertilizers. The performance of biochar derived from the pyrolysis of various types of agroindustrial wastes have been tested and identified as a reliable carrier for the microbial inoculants. The viability of microbial inoculants, their concentrations, storage stability and shelf life are some of the common factors often studied together [178,179].
Apart from the co-inoculation approach, protein hydrolysates derived from the microbial degradation of chicken feathers was tested as foliar spray for its plant growth ability on vegetable crops [60]. While different modes of fertilizer supplementation have been for microbial biofertilizers and liquid digestates from anaerobic digestion or composting, it has not been evaluated extensively for liquid fertilizers from microbially valorised wastes. Soil amendment or irrigation of roots seem to be the most preferred or researched mode of supplementation. More research is needed to identify the impact of mode of supplementation on crop yield and pest control.
Though studies that utilize microorganisms with diverse enzymatic and solubility properties have been performed, very few have validated the potential of their digestate or fermented products through plant growth tests. Identifying the prospect of a digestate to act as a “bio-organic” fertilizer by their composition of NPK can be considered insufficient, as the availability of the NPK to plants cannot be guaranteed. Similarly, many studies have performed pot- or plot-based random block design-based experiments using combinations of microbial inoculum along with waste biomass.

4.6. Lacunae in Biofertilizer Research

While the isolation and characterization of plant growth promoting bacteria and fungi were numerous, their application for bioconversion of wastes into digestates and biofertilizers was comparatively low. Moreover, functional gene studies that linked an appropriate molecular marker to certain plant growth-promoting factors such as phosphate solubilization, heavy metal accumulation, ligninocellulose-, chitinolytic-, and keratinolytic- gene clusters were also not abundant. Similarly, most of the pot and plant-based plant growth studies were conducted in natural conditions or soil systems that mimicked natural conditions. Studies that focussed on the application of biofertilizers or microbial inoculants on contaminated soils were comparatively lower. While many studies tested the bioformulation variants of their microbial inoculant using peat and biochar as carriers, it is unknown from the available documentation whether an appropriate risk assessment was conducted before its deliberate environmental release. Especially in plot tests of digested wastes containing microbial inoculants, it seems necessary to adopt quality assessment and antibiotic resistance testing of the formulation, which is restricted to AD studies of sewage sludge and associated wastes.

5. Conclusions

While this study is by no means exhaustive, it is a timely indicator that the production of sustainable biofertilizers by the valorization of waste through the application of a varied spectrum of microorganisms is a successful, yet less pursued strategy. Preference for algal nutrient recovery from wastewater streams has been observed among researchers in waste valorization, as well as restrictive to agro-economical countries such as India and China.

Author Contributions

Conceptualization, J.M.K.N. and A.S.; software, J.M.K.N.; data curation, J.M.K.N.; writing—original draft preparation, J.M.K.N.; writing—review and editing, A.S.; supervision, A.S.; funding acquisition, A.S. All authors have read and agreed to the published version of the manuscript.

Funding

This project is financed in part within the framework of the National Centre for Research and Development in Poland within the framework of a grant entitled: Biofortification of plant biomass with selenium by utilization of biofertilizers obtained via microbiological solubilisation—BioSeFert”. This research was funded in part by the National Science Centre, Poland—Grant No. 2020/39/O/ST10/02783 and Grant No. 2021/42/E/ST10/00379. For the purpose of Open Access, the author has applied a CC-BY public copyright licence to any Author Accepted Manuscript (AAM) version arising from this submission.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Wu, H.; Ge, Y. Excessive application of fertilizer, agricultural non-point source pollution, and farmers’ policy choice. Sustainability 2019, 11, 1165. [Google Scholar]
  2. Srivastav, A.L. Chemical fertilizers and pesticides: Role in groundwater contamination. In Agrochemicals Detection, Treatment and Remediation; Butterworth-Heinemann: Oxford, UK, 2020; pp. 143–159. [Google Scholar]
  3. Jiang, Y.; Chen, S.; Hu, B.; Zhou, Y.; Liang, Z.; Jia, X.; Shi, Z. A comprehensive framework for assessing the impact of potential agricultural pollution on grain security and human health in economically developed areas. Environ. Pollut. 2020, 263, 114653. [Google Scholar] [CrossRef]
  4. Zhang, T.; Yang, Y.; Ni, J.; Xie, D. Adoption behavior of cleaner production techniques to control agricultural non-point source pollution: A case study in the Three Gorges Reservoir Area. J. Clean. Prod. 2019, 223, 897–906. [Google Scholar] [CrossRef]
  5. Mitter, E.K.; Tosi, M.; Obregón, D.; Dunfield, K.E.; Germida, J.J. Rethinking crop nutrition in times of modern microbiology: Innovative biofertilizer technologies. Front. Sustain. Food Syst. 2021, 5, 606815. [Google Scholar] [CrossRef]
  6. Raimi, A.; Roopnarain, A.; Adeleke, R. Biofertilizer production in Africa: Current status, factors impeding adoption and strategies for success. Sci. Afr. 2021, 11, e00694. [Google Scholar] [CrossRef]
  7. Ma, Y.; Shen, Y.; Liu, Y. Food Waste to Biofertilizer: A Potential Game Changer of Global Circular Agricultural Economy. J. Agric. Food Chem. 2020, 68, 5021–5023. [Google Scholar] [CrossRef]
  8. Hakeem, K.R.; Dar, G.H.; Mehmood, M.A.; Bhat, R.A. (Eds.) Microbiota and Biofertilizers: A Sustainable Continuum for Plant and Soil Health; Springer International Publishing: Berlin/Heidelberg, Germany, 2021. [Google Scholar]
  9. Bhattacharyya, C.; Roy, R.; Tribedi, P.; Ghosh, A.; Ghosh, A. Biofertilizers as substitute to commercial agrochemicals. In Agrochemicals Detection, Treatment and Remediation; Butterworth-Heinemann: Oxford, UK, 2020; pp. 263–290. [Google Scholar]
  10. Lesueur, D.; Deaker, R.; Herrmann, L.; Bräu, L.; Jansa, J. The production and potential of biofertilizers to improve crop yields. In Bioformulations: For Sustainable Agriculture; Springer: New Delhi, India, 2016; pp. 71–92. [Google Scholar]
  11. Malusá, E.; Sas-Paszt, L.; Ciesielska, J. Technologies for beneficial microorganisms inocula used as biofertilizers. Sci. World J. 2012, 2012, 491206. [Google Scholar] [CrossRef]
  12. Puglia, D.; Pezzolla, D.; Gigliotti, G.; Torre, L.; Bartucca, M.L.; Del Buono, D. The opportunity of valorizing agricultural waste, through its conversion into biostimulants, biofertilizers, and biopolymers. Sustainability 2021, 13, 2710. [Google Scholar] [CrossRef]
  13. Du, C.; Abdullah, J.J.; Greetham, D.; Fu, D.; Yu, M.; Ren, L.; Lu, D. Valorization of food waste into biofertiliser and its field application. J. Clean. Prod. 2018, 187, 273–284. [Google Scholar] [CrossRef] [Green Version]
  14. Wang, X.; Li, C.; Lam, C.H.; Subramanian, K.; Qin, Z.H.; Mou, J.H.; Lin, C.S.K. Emerging waste valorisation techniques to moderate the hazardous impacts, and their path towards sustainability. J. Hazard. Mater. 2022, 423, 127023. [Google Scholar] [CrossRef]
  15. Jimenez-Lopez, C.; Fraga-Corral, M.; Carpena, M.; García-Oliveira, P.; Echave, J.; Pereira, A.G.; Simal-Gandara, J. Agriculture waste valorisation as a source of antioxidant phenolic compounds within a circular and sustainable bioeconomy. Food Funct. 2020, 11, 4853–4877. [Google Scholar] [CrossRef]
  16. Arancon, R.A.D.; Lin, C.S.K.; Chan, K.M.; Kwan, T.H.; Luque, R. Advances on waste valorization: New horizons for a more sustainable society. Energy Sci. Eng. 2013, 1, 53–71. [Google Scholar] [CrossRef]
  17. Cho, E.J.; Trinh, L.T.P.; Song, Y.; Lee, Y.G.; Bae, H.J. Bioconversion of biomass waste into high value chemicals. Bioresour. Technol. 2020, 298, 122386. [Google Scholar] [CrossRef]
  18. Antunes, L.P.; Martins, L.F.; Pereira, R.V.; Thomas, A.M.; Barbosa, D.; Lemos, L.N.; Setubal, J.C. Microbial community structure and dynamics in thermophilic composting viewed through metagenomics and metatranscriptomics. Sci. Rep. 2016, 6, 1–13. [Google Scholar] [CrossRef] [Green Version]
  19. Huang, S.; Zheng, X.; Luo, L.; Ni, Y.; Yao, L.; Ni, W. Biostimulants in bioconversion compost of organic waste: A novel booster in sustainable agriculture. J. Clean. Prod. 2021, 319, 128704. [Google Scholar] [CrossRef]
  20. Canfora, L.; Costa, C.; Pallottino, F.; Mocali, S. Trends in soil microbial inoculants research: A science mapping approach to unravel strengths and weaknesses of their application. Agriculture 2021, 11, 158. [Google Scholar] [CrossRef]
  21. Van Eck, N.; Waltman, L. Software survey: VOSviewer, a computer program for bibliometric mapping. Scientometrics 2010, 84, 523–538. [Google Scholar] [CrossRef] [Green Version]
  22. Richardson, W.S.; Wilson, M.C.; Nishikawa, J.; Hayward, R.S. The well-built clinical question: A key to evidence-based decisions. Acp J Club 1995, 123, A12–A13. [Google Scholar] [CrossRef]
  23. Page, M.J.; McKenzie, J.E.; Bossuyt, P.M.; Boutron, I.; Hoffmann, T.C.; Mulrow, C.D.; Moher, D. The PRISMA 2020 statement: An updated guideline for reporting systematic reviews. Syst. Rev. 2021, 10, 1–11. [Google Scholar] [CrossRef]
  24. Biswas, T.; Chatterjee, D.; Barman, S.; Chakraborty, A.; Halder, N.; Banerjee, S.; Chaudhuri, S.R. Cultivable bacterial community analysis of dairy activated sludge for value addition to dairy wastewater. Microbiol. Biotechnol. Lett. 2019, 47, 585–595. [Google Scholar] [CrossRef]
  25. Jastrzębska, M.; Saeid, A.; Kostrzewska, M.K.; Baśladyńska, S. New phosphorus biofertilizers from renewable raw materials in the aspect of cadmium and lead contents in soil and plants. Open Chem. 2018, 16, 35–49. [Google Scholar] [CrossRef]
  26. Xiao, X.; Mazza, L.; Yu, Y.; Cai, M.; Zheng, L.; Tomberlin, J.K.; Zhang, J. Efficient co-conversion process of chicken manure into protein feed and organic fertilizer by Hermetia illucens L. (Diptera: Stratiomyidae) larvae and functional bacteria. J. Environ. Manag. 2018, 217, 668–676. [Google Scholar] [CrossRef]
  27. Stamford, N.P.; Silva, E.V.N.D.; Oliveira, W.D.S.; Silva, M.C.F.D.; Martins, M.D.S.; Silva, V.S.G.D. Organic matter inoculated with diazotrophic bacterium Beijerinckia indica and Cunninghamella elegans fungus containing chitosan on banana” Williams” in field. Acta Scientiarum. Agronomy 2017, 39, 33–41. [Google Scholar]
  28. Piskaeva, A.I.; Babich, O.O.; Dolganyuk, V.F.; Garmashov, S.Y. Analysis of influence of biohumus on the basis of consortium of effective microorganisms on the productivity of winter wheat. Foods Raw Mater. 2017, 5, 90–99. [Google Scholar] [CrossRef]
  29. Jastrzuska, M.; Kostrzewska, M.K.; Saeid, A.; Treder, K.; Makowski, P.; Jastrzwski, W.P.; Okorski, A. Granulated phosphorus fertilizer made of ash from biomass combustion and bones with addition of Bacillus megaterium in the field assessment. Part 1. Impact on yielding and sanitary condition of winter wheat. Przem. Chem. 2017, 96, 2168–2174. [Google Scholar]
  30. Wyciszkiewicz, M.; Saeid, A.; Samoraj, M.; Chojnacka, K. Solid-state solubilization of bones by B. megaterium in spent mushroom substrate as a medium for a phosphate enriched substrate. J. Chem. Technol. Biotechnol. 2017, 92, 1397–1405. [Google Scholar] [CrossRef]
  31. Tyśkiewicz, R.; Nowak, A.; Ozimek, E.; Jaroszuk-Ściseł, J. Trichoderma: The current status of its application in agriculture for the biocontrol of fungal phytopathogens and stimulation of plant growth. Int. J. Mol. Sci. 2022, 23, 2329. [Google Scholar] [CrossRef]
  32. Naik, K.; Mishra, S.; Srichandan, H.; Singh, P.K.; Sarangi, P.K. Plant growth promoting microbes: Potential link to sustainable agriculture and environment. Biocatal. Agric. Biotechnol. 2019, 21, 101326. [Google Scholar] [CrossRef]
  33. Win, T.T.; Barone, G.D.; Secundo, F.; Fu, P. Algal biofertilizers and plant growth stimulants for sustainable agriculture. Ind. Biotechnol. 2018, 14, 203–211. [Google Scholar] [CrossRef]
  34. Asadu, C.O.; Aneke, N.G.; Egbuna, S.O.; Agulanna, A.C. Comparative studies on the impact of bio-fertilizer produced from agro-wastes using thermo-tolerant actinomycetes on the growth performance of Maize (Zea mays) and Okro (Abelmoschus esculentus). Environ. Technol. Innov. 2018, 12, 55–71. [Google Scholar] [CrossRef]
  35. Dini, I.R.; Salbiah, D.; Tryana, S. Application of biofertilizer consortium formulation of cellulolytic bacteria based on organic liquid waste on yield of upland rice (Oryza sativa L.). IOP Conf. Ser. Earth Environ. Sci. 2020, 454, 012142. [Google Scholar]
  36. Peña García, P.; Querevalú Ortiz, J.; Ochoa Mogollón, G.; Sánchez Suárez, H. Biological silage of shrimp waste fermented with lactic acid bacteria: Use as a biofertilizer in pasture crops and as feed for backyard pigs. Sci. Agropecu. 2020, 11, 459–471. [Google Scholar] [CrossRef]
  37. Chintagunta, A.D.; Kumar, S.J.; Krishna, M.S.; Addanki, M.; Kumar, N.S.S. Studies on bioconversion of agri-waste to biomanure. Indian J. Ecol. 2020, 47, 116–121. [Google Scholar]
  38. Das, P.; Quadir, M.A.; Thaher, M.I.; Alghasal, G.S.H.S.; Aljabri, H.M.S.J. Microalgal nutrients recycling from the primary effluent of municipal wastewater and use of the produced biomass as bio-fertilizer. Int. J. Environ. Sci. Technol. 2019, 16, 3355–3364. [Google Scholar] [CrossRef]
  39. Thiyageshwari, S.; Gayathri, P.; Krishnamoorthy, R.; Anandham, R.; Paul, D. Exploration of rice husk compost as an alternate organic manure to enhance the productivity of black gram in typic haplustalf and typic rhodustalf. Int. J. Environ. Res. Public Health 2018, 15, 358. [Google Scholar] [CrossRef]
  40. Ahmad, J. Bioremediation of petroleum sludge using effective microorganism (EM) technology. Pet. Sci. Technol. 2017, 35, 1515–1522. [Google Scholar] [CrossRef]
  41. Abirami, S.; Ragavi, R.; Antony, V.S. Utilization of keratinolytic Lichtheimia corymbifera AS1 for degradation of cattle hoove—A slaughter house waste to use in plant growth. Biointerface Res. Appl. Chem. 2020, 10, 6417–6426. [Google Scholar]
  42. Abou-Zeid, H.; El-Darier, S.; Ghanem, K.; Salah, A. Fertilizing Potentiality of Fungal-Treated Olive Mill Solid Waste to Improve Some Growth and Physiological Parameters of Vicia faba L. Egypt. J. Bot. 2020, 60, 691–705. [Google Scholar] [CrossRef]
  43. Al-Dhabi, N.A.; Esmail, G.A.; Mohammed Ghilan, A.K.; Valan Arasu, M. Composting of vegetable waste using microbial consortium and biocontrol efficacy of Streptomyces Sp. Al-Dhabi 30 isolated from the Saudi Arabian environment for sustainable agriculture. Sustainability 2019, 11, 6845. [Google Scholar] [CrossRef] [Green Version]
  44. Ameen, F.; Al-Homaidan, A.A. Compost inoculated with fungi from a mangrove habitat improved the growth and disease defense of vegetable plants. Sustainability 2020, 13, 124. [Google Scholar] [CrossRef]
  45. Asadu, C.O.; Ike, I.S.; Onu, C.E.; Egbuna, S.O.; Onoh, M.; Mbah, G.O.; Eze, C.N. Investigation of the influence of biofertilizer synthesized using microbial inoculums on the growth performance of two agricultural crops. Biotechnol. Rep. 2020, 27, e00493. [Google Scholar] [CrossRef]
  46. Bedi, A.; Singh, B.R.; Deshmukh, S.K.; Aggarwal, N.; Barrow, C.J.; Adholeya, A. Development of a novel myconanomining approach for the recovery of agriculturally important elements from jarosite waste. J. Environ. Sci. 2018, 67, 356–367. [Google Scholar] [CrossRef]
  47. Biswas, I.; Mitra, D.; Senapati, A.; Mitra, D.; Chattaraj, S.; Ali, M.; Das Mohapatra, P.K. Valorization of vermicompost with bacterial fermented chicken feather hydrolysate for the yield improvement of tomato plant: A novel organic combination. Int. J. Recycl. Org. Waste Agric. 2021, 10, 29–42. [Google Scholar]
  48. Łaba, W.; Żarowska, B.; Chorążyk, D.; Pudło, A.; Piegza, M.; Kancelista, A.; Kopeć, W. New keratinolytic bacteria in valorization of chicken feather waste. AMB Express 2018, 8, 1–14. [Google Scholar] [CrossRef] [Green Version]
  49. Cárcamo, L.; Sierra, S.; Osorio, M.; Velásquez-Cock, J.; Vélez-Acosta, L.; Gómez-Hoyos, C.; Gañán, P. Bacterial nanocellulose mulch as a potential greener alternative for urban gardening in the small-scale food production of onion plants. Agric. Res. 2021, 10, 66–71. [Google Scholar] [CrossRef]
  50. Chen, Y.; Jiang, Z.; Wu, D.; Wang, H.; Li, J.; Bi, M.; Zhang, Y. Development of a novel bio-organic fertilizer for the removal of atrazine in soil. J. Environ. Manag. 2019, 233, 553–560. [Google Scholar] [CrossRef]
  51. Dimitrijević, S.; Radanović, D.S.; Antić-Mladenović, S.B.; Milutinović, M.; Rajilić-Stojanović, M.; Dimitrijević-Branković, S. Enhanced fertilization effect of a compost obtained from mixed herbs waste inoculated with novel strains of mesophilic bacteria. Hem. Ind. 2017, 71, 503–513. [Google Scholar] [CrossRef]
  52. Emmanuel, S.A.; Yoo, J.; Kim, E.J.; Chang, J.S.; Park, Y.I.; Koh, S.C. Development of functional composts using spent coffee grounds, poultry manure and biochar through microbial bioaugmentation. J. Environ. Sci. Health Part B 2017, 52, 802–811. [Google Scholar] [CrossRef]
  53. Feng, N.X.; Liang, Q.F.; Feng, Y.X.; Xiang, L.; Zhao, H.M.; Li, Y.W.; Wong, M.H. Improving yield and quality of vegetable grown in PAEs-contaminated soils by using novel bioorganic fertilizer. Sci. Total Environ. 2020, 739, 139883. [Google Scholar] [CrossRef]
  54. Ferreira, A.; Ribeiro, B.; Ferreira, A.F.; Tavares, M.L.; Vladic, J.; Vidović, S.; Gouveia, L. Scenedesmus obliquus microalga-based biorefinery–from brewery effluent to bioactive compounds, biofuels and biofertilizers–aiming at a circular bioeconomy. Biofuels Bioprod. Biorefining 2019, 13, 1169–1186. [Google Scholar] [CrossRef]
  55. Gao, H.; Lu, C.; Wang, H.; Wang, L.; Yang, Y.; Jiang, T.; Wu, L. Production exopolysaccharide from Kosakonia cowanii LT-1 through solid-state fermentation and its application as a plant growth promoter. Int. J. Biol. Macromol. 2020, 150, 955–964. [Google Scholar] [CrossRef]
  56. Gaonkar, S.K.; Furtado, I.J. Biorefinery-Fermentation of Agro-Wastes by Haloferax lucentensis GUBF-2 MG076878 to Haloextremozymes for use as Biofertilizer and Biosynthesizer of AgNPs. Waste Biomass Valorization 2022, 13, 1117–1133. [Google Scholar] [CrossRef]
  57. Gemin, L.G.; Mógor, Á.F.; Mógor, G.; Roder, C.; Szilagyi-Zecchin, V.J. Cambios en el crecimiento y concentración de aminoácidos en las plántulas de col china usando caldo bacteriano fermentado. Idesia 2018, 36, 7–13. [Google Scholar] [CrossRef] [Green Version]
  58. González, I.; Ekelhof, A.; Herrero, N.; Siles, J.Á.; Podola, B.; Chica, A.F.; Gómez, J.M. Wastewater nutrient recovery using twin-layer microalgae technology for biofertilizer production. Water Sci. Technol. 2020, 82, 1044–1061. [Google Scholar] [CrossRef]
  59. Gunjal, A.B.; Kapadnis, B.P.; Pawar, N.J. Pressmud, a lignocellulosic waste as potential carrier for in-situ production of plant growth promoting substances by Bacillus circulans. J. Solid Waste Technol. Manag. 2018, 44, 281–287. [Google Scholar] [CrossRef]
  60. Gurav, R.; Nalavade, V.; Aware, C.; Vyavahare, G.; Bhatia, S.K.; Yang, Y.H.; Jadhav, J. Microbial degradation of poultry feather biomass in a constructed bioreactor and application of hydrolysate as bioenhancer to vegetable crops. Environ. Sci. Pollut. Res. 2020, 27, 2027–2035. [Google Scholar] [CrossRef]
  61. Hadidi, M.; Bahlaouan, B.; Asbai, Z.; Radi Benjelloun, G.; El Antri, S.; Boutaleb, N. Optimizing biogas and biofertilizer production from abundant Moroccan industrial organic wastes by the formulation and the use of a fungal inoculum. Adv. Environ. Technol. 2021, 7, 275–287. [Google Scholar]
  62. Gandhi, A.; Sivakumar, K. Impact of vermicompost carrier based bioinoculants on the growth, yield and quality of rice (Oryza sativa L.) CV NLR 145. Ecoscan 2010, 4, 83–88. [Google Scholar]
  63. Hasan, Z.A.E.; Mohd Zainudin, N.A.I.; Aris, A.; Ibrahim, M.H.; Yusof, M.T. Biocontrol efficacy of Trichoderma asperellum-enriched coconut fibre against Fusarium wilts of cherry tomato. J. Appl. Microbiol. 2020, 129, 991–1003. [Google Scholar] [CrossRef]
  64. Huang, J.; Zhuo, Y.; Lu, J.; Lai, Q.; Zhang, Y. Bacillus cereus liquid fertilizer was produced from Agaricus bisporus industrial wastewater. J. Biotechnol. 2021, 327, 74–85. [Google Scholar] [CrossRef]
  65. Hussain, A.; Zahir, Z.A.; Ditta, A.; Tahir, M.U.; Ahmad, M.; Mumtaz, M.Z.; Hussain, S. Production and implication of bio-activated organic fertilizer enriched with zinc-solubilizing bacteria to boost up maize (Zea mays L.) production and biofortification under two cropping seasons. Agronomy 2019, 10, 39. [Google Scholar] [CrossRef] [Green Version]
  66. Ilangumaran, G.; Stratton, G.; Ravichandran, S.; Shukla, P.S.; Potin, P.; Asiedu, S.; Prithiviraj, B. Microbial degradation of lobster shells to extract chitin derivatives for plant disease management. Front. Microbiol. 2017, 8, 781. [Google Scholar] [CrossRef] [Green Version]
  67. Irawan, B.; Zulkifli, Z.; Handayani, T.T.; Hadi, S. Effect of induced compost by cellulolitic (Aspergillus fumigatus) and ligninolitic (geotrichum sp.) fungi inoculum application on vegetative growth of red chili (Capsicum annuum L.). J. Pure Appl. Microbiol. 2019, 13, 815–821. [Google Scholar] [CrossRef] [Green Version]
  68. Jastrzębska, M.; Kostrzewska, M.K.; Treder, K. Phosphorus fertilizers from sewage sludge ash and animal blood have no effect on earthworms. Agronomy 2020, 10, 525. [Google Scholar] [CrossRef] [Green Version]
  69. Kumar, J.; Kumar, P.; Kushwaha, R.K.S. Recycling of chicken feather protein into compost by Chrysosporium indicum JK14 and their effect on the growth promotion of Zea mays. Plant Cell Biotechnol. Mol. Biol. 2020, 21, 75–80. [Google Scholar]
  70. Kumari, M.; Kumar, J. Chicken feather waste degradation by Alternaria tenuissima and its application on plant growth. J. Appl. Nat. Sci. 2020, 12, 411–414. [Google Scholar] [CrossRef]
  71. Li, Y.; Cui, T.; Wang, Y.; Ge, X. Isolation and characterization of a novel bacterium Pseudomonas aeruginosa for biofertilizer production from kitchen waste oil. RSC Adv. 2018, 8, 41966–41975. [Google Scholar] [CrossRef] [Green Version]
  72. Li, L.; Chen, R.; Zuo, Z.; Lv, Z.; Yang, Z.; Mao, W.; Song, Z. Evaluation and improvement of phosphate solubilization by an isolated bacterium Pantoea agglomerans ZB. World J. Microbiol. Biotechnol. 2020, 36, 1–14. [Google Scholar] [CrossRef]
  73. Lopes, C.M.; Silva, A.M.M.; Estrada-Bonilla, G.A.; Ferraz-Almeida, R.; Vieira, J.L.V.; Otto, R.; Cardoso, E.J.B.N. Improving the fertilizer value of sugarcane wastes through phosphate rock amendment and phosphate-solubilizing bacteria inoculation. J. Clean. Prod. 2021, 298, 126821. [Google Scholar] [CrossRef]
  74. Mahmood, A.; Iguchi, R.; Kataoka, R. Multifunctional food waste fertilizer having the capability of Fusarium-growth inhibition and phosphate solubility: A new horizon of food waste recycle using microorganisms. Waste Manag. 2019, 94, 77–84. [Google Scholar] [CrossRef]
  75. Naeem, U.; Afzaal, M.; Qazi, A.; Yasar, A.; Mahfooz, Y.; Naz, A.U.; Awan, H. Investigating the effect of Aspergillus niger inoculated press mud (biofertilizer) on the potential of enhancing maize (Zea mays L.) yield, potassium use efficiency and potassium agronomic efficiency. Cereal Res. Commun. 2022, 50, 157–170. [Google Scholar] [CrossRef]
  76. Nagarajan, S.; Eswaran, P.; Masilamani, R.P.; Natarajan, H. Chicken feather compost to promote the plant growth activity by using keratinolytic bacteria. Waste Biomass Valorization 2018, 9, 531–538. [Google Scholar] [CrossRef]
  77. Naher, U.A.; Biswas, J.C.; Maniruzzaman, M.; Khan, F.H.; Sarkar, M.I.U.; Jahan, A.; Kabir, M.S. Bio-organic fertilizer: A green technology to reduce synthetic N and P fertilizer for rice production. Front. Plant Sci. 2021, 12, 602052. [Google Scholar] [CrossRef]
  78. Nasarudin, A.A.; Ngadi, N.; Yusoff, N.A.; Ali, N.; Aziz, M.A.A.; Rahman, R.A. Production of biofertilizer using Lactobacillus inoculants and glycerin pitch from oleochemical industry. IOP Conf. Ser. Mater. Sci. Eng. 2020, 736, 022105. [Google Scholar] [CrossRef]
  79. Nayak, M.; Swain, D.K.; Sen, R. Strategic valorization of de-oiled microalgal biomass waste as biofertilizer for sustainable and improved agriculture of rice (Oryza sativa L.) crop. Sci. Total Environ. 2019, 682, 475–484. [Google Scholar] [CrossRef]
  80. Ntsobi, N.; Fanadzo, M.; Le Roes-Hill, M.; Nchu, F. Effects of Clonostachys rosea f. Catenula inoculum on the composting of cabbage wastes and the endophytic activities of the composted material on tomatoes and red spider mite infestation. Microorganisms 2021, 9, 1184. [Google Scholar] [CrossRef]
  81. Nunes Oliveira, F.L.; Silva Oliveira, W.; Pereira Stamford, N.; Nova Silva, E.V.; Santiago Freitas, A.D. Effectiveness of biofertilizer enriched in N by Beijerinckia indica on sugarcane grown on an Ultisol and the interactive effects between biofertilizer and sugarcane filter cake. J. Soil Sci. Plant Nutr. 2017, 17, 1040–1057. [Google Scholar] [CrossRef] [Green Version]
  82. Pal, K.; Rakshit, S.; Mondal, K.C.; Halder, S.K. Microbial decomposition of crustacean shell for production of bioactive metabolites and study of its fertilizing potential. Environ. Sci. Pollut. Res. 2021, 28, 58915–58928. [Google Scholar] [CrossRef]
  83. Parastesh, F.; Alikhani, H.A.; Etesami, H. Vermicompost enriched with phosphate–solubilizing bacteria provides plant with enough phosphorus in a sequential cropping under calcareous soil conditions. J. Clean. Prod. 2019, 221, 27–37. [Google Scholar] [CrossRef]
  84. Pascual, J.A.; Bernal-Vicente, A.; Martinez-Medina, A.; Ros, M.; Sánchez, C. Biostimulant and suppressive effect of Trichoderma harzianum enriched compost for melon cultivation from greenhouse nursery to field production. In Proceedings of the III International Symposium on Organic Greenhouse Horticulture 1164, Izmir, Turkey, 11–14 April 2016; pp. 225–232. [Google Scholar]
  85. Patil, P.M.; Mahamuni, P.P.; Abdel-Daim, M.M.; Aleya, L.; Chougule, R.A.; Shadija, P.G.; Bohara, R.A. Conversion of organic biomedical waste into potential fertilizer using isolated organisms from cow dung for a cleaner environment. Environ. Sci. Pollut. Res. 2019, 26, 27897–27904. [Google Scholar] [CrossRef]
  86. Raymond, N.S.; Jensen, L.S.; Stöver, D.M. Enhancing the phosphorus bioavailability of thermally converted sewage sludge by phosphate-solubilising fungi. Ecol. Eng. 2018, 12, 44–53. [Google Scholar] [CrossRef]
  87. Röder, C.; Mógor, Á.F.; Szilagyi-Zecchin, V.J.; Gemin, L.G.; Mógor, G. Potato yield and metabolic changes by use of biofertilizer containing L-glutamic acid. Comun. Sci. 2018, 9, 211–218. [Google Scholar] [CrossRef]
  88. Saeid, A.; Patel, A. Valorization of ash and spent mushroom substrate via solid-state solubilization by Acidithiobacillus ferrooxidans. Waste Manag. 2019, 87, 612–620. [Google Scholar] [CrossRef]
  89. Santhanarajan, A.E.; Han, Y.H.; Koh, S.C. The Efficacy of Functional Composts Manufactured Using Spent Coffee Ground, Rice Bran, Biochar, and Functional Microorganisms. Appl. Sci. 2021, 11, 7703. [Google Scholar] [CrossRef]
  90. Shen, T.; Lei, Y.; Pu, X.; Zhang, S.; Du, Y. Identification and application of Streptomyces microflavus G33 in compost to suppress tomato bacterial wilt disease. Appl. Soil Ecol. 2021, 157, 103724. [Google Scholar] [CrossRef]
  91. Silambarasan, S.; Logeswari, P.; Sivaramakrishnan, R.; Incharoensakdi, A.; Cornejo, P.; Kamaraj, B.; Chi, N.T.L. Removal of nutrients from domestic wastewater by microalgae coupled to lipid augmentation for biodiesel production and influence of deoiled algal biomass as biofertilizer for Solanum lycopersicum cultivation. Chemosphere 2021, 268, 129323. [Google Scholar] [CrossRef]
  92. Singh, U.B.; Malviya, D.; Khan, W.; Singh, S.; Karthikeyan, N.; Imran, M.; Oh, J.W. Earthworm grazed-Trichoderma harzianum biofortified spent mushroom substrates modulate accumulation of natural antioxidants and bio-fortification of mineral nutrients in tomato. Front. Plant Sci. 2018, 9, 1017. [Google Scholar] [CrossRef]
  93. Stanley-Raja, V.; Senthil-Nathan, S.; Chanthini, K.M.P.; Sivanesh, H.; Ramasubramanian, R.; Karthi, S.; Kalaivani, K. Biological activity of chitosan inducing resistance efficiency of rice (Oryza sativa L.) after treatment with fungal based chitosan. Sci. Rep. 2021, 11, 1–15. [Google Scholar] [CrossRef]
  94. Suleiman, A.K.A.; Lourenço, K.S.; Clark, C.; Luz, R.L.; da Silva, G.H.R.; Vet, L.E.; Kuramae, E.E. From toilet to agriculture: Fertilization with microalgal biomass from wastewater impacts the soil and rhizosphere active microbiomes, greenhouse gas emissions and plant growth. Resour. Conserv. Recycl. 2020, 161, 104924. [Google Scholar] [CrossRef]
  95. Sun, Z.; Li, X.; Liu, K.; Chi, X.; Liu, L. Optimization for production of a plant growth promoting agent from the degradation of chicken feather using keratinase producing novel isolate Bacillus pumilus JYL. Waste Biomass Valorization 2021, 12, 1943–1954. [Google Scholar] [CrossRef]
  96. Umamaheswari, J.; Shanthakumar, S. Paddy-soaked rice mill wastewater treatment by phycoremediation and feasibility study on use of algal biomass as biofertilizer. J. Chem. Technol. Biotechnol. 2021, 96, 394–403. [Google Scholar] [CrossRef]
  97. Unnikrishnan, G.; Vijayaraghavan, R. Evaluation of lignin waste as potential carriers for phosphate solubilizing bio-fertilizers: A zero waste technology. Int. J. Recycl. Org. Waste Agric. 2021, 10, 331–351. [Google Scholar]
  98. Zeng, Y.H.; Kuo, Y.W.; Chen, H.T. Higher yield of cherry tomato grown in culture medium with microbially inoculated feather compost without fertilizer application. J. Plant Nutr. Soil Sci. 2018, 181, 528–536. [Google Scholar] [CrossRef]
  99. Zhang, H.; Hua, Z.W.; Liang, W.Z.; Niu, Q.H.; Wang, X. The Prevention of Bio-Organic Fertilizer Fermented from Cow Manure Compost by Bacillus sp. XG-1 on Watermelon Continuous Cropping Barrier. Int. J. Environ. Res. Public Health 2020, 17, 5714. [Google Scholar] [CrossRef] [PubMed]
  100. Zhang, X.; Wang, Y.; Han, X.; Gou, J.; Li, W.; Zhang, C. A novel bio-fertilizer produced by prickly ash seeds with biochar addition induces soil suppressiveness against black shank disease on tobacco. Appl. Sci. 2021, 11, 7261. [Google Scholar] [CrossRef]
  101. Jamison, J.; Khanal, S.K.; Nguyen, N.H.; Deenik, J.L. Assessing the effects of digestates and combinations of digestates and fertilizer on yield and nutrient use of Brassica juncea (Kai Choy). Agronomy 2021, 11, 509. [Google Scholar] [CrossRef]
  102. Pottipati, S.; Chakma, R.; Haq, I.; Kalamdhad, A.S. Composting and vermicomposting: Process optimization for the management of organic waste. In Advanced Organic Waste Management; Elsevier: Amsterdam, The Netherlands, 2022; pp. 33–43. [Google Scholar]
  103. Flores-Félix, J.D.; Menéndez, E.; Rivas, R.; de la Encarnación Velázquez, M. Future perspective in organic farming fertilization: Management and product. In Organic Farming; Woodhead Publishing: Cambridge, MA, USA, 2019; pp. 269–315. [Google Scholar]
  104. Ayilara, M.S.; Olanrewaju, O.S.; Babalola, O.O.; Odeyemi, O. Waste management through composting: Challenges and potentials. Sustainability 2020, 12, 4456. [Google Scholar] [CrossRef]
  105. Nguyen, T.K.X.; Thayanukul, P.; Pinyakong, O.; Suttinun, O. Tiamulin removal by wood-rot fungi isolated from swine farms and role of ligninolytic enzymes. Int. Biodeterior. Biodegrad. 2017, 116, 147–154. [Google Scholar] [CrossRef]
  106. Pan, L.J.; Li, J.; Li, C.X.; Yu, G.W.; Wang, Y. Study of ciprofloxacin biodegradation by a Thermus sp. isolated from pharmaceutical sludge. J. Hazard. Mater. 2018, 343, 59–67. [Google Scholar] [CrossRef]
  107. Setiawati, M.R.; Suryatmana, P.; Hindersah, R.; Kamaluddin, N.; Efendi, S. The effectiveness of various compositions lignolytic and cellulolytic microbes in composting empty fruit bunch palm oil and sugar cane biomass. IOP Conf. Ser. Earth Environ. Sci. 2019, 393, 012032. [Google Scholar] [CrossRef]
  108. Nakasaki, K.; Hirai, H.; Mimoto, H.; Quyen, T.N.M.; Koyama, M.; Takeda, K. Succession of microbial community during vigorous organic matter degradation in the primary fermentation stage of food waste composting. Sci. Total Environ. 2019, 671, 1237–1244. [Google Scholar] [CrossRef]
  109. Duan, Y.; Awasthi, S.K.; Liu, T.; Pandey, A.; Zhang, Z.; Kumar, S.; Awasthi, M.K. Succession of keratin-degrading bacteria and associated health risks during pig manure composting. J. Clean. Prod. 2020, 258, 120624. [Google Scholar] [CrossRef]
  110. Song, S.; Lim, J.W.; Lee, J.T.; Cheong, J.C.; Hoy, S.H.; Hu, Q.; Tong, Y.W. Food-waste anaerobic digestate as a fertilizer: The agronomic properties of untreated digestate and biochar-filtered digestate residue. Waste Manag. 2021, 136, 143–152. [Google Scholar] [CrossRef] [PubMed]
  111. Tallou, A.; Salcedo, F.P.; Haouas, A.; Jamali, M.Y.; Atif, K.; Aziz, F.; Amir, S. Assessment of biogas and biofertilizer produced from anaerobic co-digestion of olive mill wastewater with municipal wastewater and cow dung. Environ. Technol. Innov. 2020, 20, 101152. [Google Scholar] [CrossRef]
  112. Cucina, M.; Castro, L.; Escalante, H.; Ferrer, I.; Garfí, M. Benefits and risks of agricultural reuse of digestates from plastic tubular digesters in Colombia. Waste Manag. 2021, 135, 220–228. [Google Scholar] [CrossRef]
  113. Yıldırım, E.; Ince, O.; Aydin, S.; Ince, B. Improvement of biogas potential of anaerobic digesters using rumen fungi. Renew. Energy 2017, 109, 346–353. [Google Scholar] [CrossRef]
  114. Golovko, O.; Ahrens, L.; Schelin, J.; Sörengård, M.; Bergstrand, K.J.; Asp, H.; Wiberg, K. Organic micropollutants, heavy metals and pathogens in anaerobic digestate based on food waste. J. Environ. Manag. 2022, 313, 114997. [Google Scholar] [CrossRef]
  115. Södergren, J.; Larsson, C.U.; Wadsö, L.; Bergstrand, K.J.; Asp, H.; Hultberg, M.; Schelin, J. Food waste to new food: Risk assessment and microbial community analysis of anaerobic digestate as a nutrient source in hydroponic production of vegetables. J. Clean. Prod. 2022, 333, 130239. [Google Scholar] [CrossRef]
  116. Ye, Y.; Ngo, H.H.; Guo, W.; Chang, S.W.; Nguyen, D.D.; Zhang, X.; Liang, S. Nutrient recovery from wastewater: From technology to economy. Bioresour. Technol. Rep. 2020, 11, 100425. [Google Scholar] [CrossRef]
  117. Acién Fernández, F.G.; Gómez-Serrano, C.; Fernández-Sevilla, J.M. Recovery of nutrients from wastewaters using microalgae. Front. Sustain. Food Syst. 2018, 2, 59. [Google Scholar] [CrossRef] [Green Version]
  118. Khan, S.A.; Sharma, G.K.; Malla, F.A.; Kumar, A.; Gupta, N. Microalgae based biofertilizers: A biorefinery approach to phycoremediate wastewater and harvest biodiesel and manure. J. Clean. Prod. 2019, 211, 1412–1419. [Google Scholar] [CrossRef]
  119. Mahapatra, D.M.; Chanakya, H.N.; Joshi, N.V.; Ramachandra, T.V.; Murthy, G.S. Algae-based biofertilizers: A biorefinery approach. In Microorganisms for Green Revolution; Springer: Singapore, 2018; pp. 177–196. [Google Scholar]
  120. Ogata-Gutiérrez, K.; Zúñiga-Dávila, D. Bacteria-Plant interactions: An added value of microbial inoculation. Rev. Peru. De Biol. 2020, 27, 021–025. [Google Scholar] [CrossRef] [Green Version]
  121. Choudhury, D.; Tarafdar, S.; Dutta, S. Plant growth promoting rhizobacteria (PGPR) and their eco-friendly strategies for plant growth regulation: A review. Plant Sci. Today 2022, 9, 3. [Google Scholar] [CrossRef]
  122. Murali, M.; Naziya, B.; Ansari, M.A.; Alomary, M.N.; Al Yahya, S.; Almatroudi, A.; Amruthesh, K.N. Bioprospecting of rhizosphere-resident fungi: Their role and importance in sustainable agriculture. J. Fungi 2021, 7, 314. [Google Scholar] [CrossRef] [PubMed]
  123. Dey, G.; Banerjee, P.; Sharma, R.K.; Maity, J.P.; Etesami, H.; Shaw, A.K.; Chen, C.Y. Management of phosphorus in salinity-stressed agriculture for sustainable crop production by salt-tolerant phosphate-solubilizing bacteria—A review. Agronomy 2021, 11, 1552. [Google Scholar] [CrossRef]
  124. Basak, B.B.; Maity, A.; Ray, P.; Biswas, D.R.; Roy, S. Potassium supply in agriculture through biological potassium fertilizer: A promising and sustainable option for developing countries. Arch. Agron. Soil Sci. 2022, 68, 101–114. [Google Scholar] [CrossRef]
  125. Kuila, D.; Ghosh, S. Aspects, problems and utilization of Arbuscular Mycorrhizal (AM) application as bio-fertilizer in sustainable agriculture. Curr. Res. Microb. Sci. 2022, 3, 100107. [Google Scholar] [CrossRef]
  126. Kumaar, S.A.; Babu, R.P.; Vivek, P.; Saravanan, D. Role of Nitrogen Fixers as Biofertilizers in Future Perspective: A Review. Res. J. Pharm. Technol. 2020, 13, 2459–2467. [Google Scholar] [CrossRef]
  127. Soumare, A.; Diedhiou, A.G.; Thuita, M.; Hafidi, M.; Ouhdouch, Y.; Gopalakrishnan, S.; Kouisni, L. Exploiting biological nitrogen fixation: A route towards a sustainable agriculture. Plants 2020, 9, 1011. [Google Scholar] [CrossRef]
  128. Adeleke, B.S.; Babalola, O.O. Biotechnological overview of agriculturally important endophytic fungi. Hortic. Environ. Biotechnol. 2021, 62, 507–520. [Google Scholar] [CrossRef]
  129. Willey, J.M.; Sandman, K.; Wood, D. Prescott’s Microbiolog, 11th ed.; McGraw-Hill: New York, NY, USA, 2022. [Google Scholar]
  130. Kapoor, M.; Panwar, D.; Kaira, G.S. Bioprocesses for enzyme production using agro-industrial wastes: Technical challenges and commercialization potential. In Agro-Industrial Wastes as Feedstock for Enzyme Production; Academic Press: Cambridge, MA, USA, 2016; pp. 61–93. [Google Scholar]
  131. Chilakamarry, C.R.; Sakinah, A.M.; Zularisam, A.W.; Sirohi, R.; Khilji, I.A.; Ahmad, N.; Pandey, A. Advances in solid-state fermentation for bioconversion of agricultural wastes to value-added products: Opportunities and challenges. Bioresour. Technol. 2022, 343, 126065. [Google Scholar] [CrossRef] [PubMed]
  132. Buntić, A.V.; Milić, M.D.; Stajković-Srbinović, O.S.; Rasulić, N.V.; Delić, D.I.; Mihajlovski, K.R. Cellulase production by Sinorhizobium meliloti strain 224 using waste tobacco as substrate. Int. J. Environ. Sci. Technol. 2019, 16, 5881–5890. [Google Scholar] [CrossRef]
  133. Riddech, N.; Sarin, P.; Phibunwatthanawong, T. Effect of bio-liquid organic fertilizer on the growth of Dipterocarpus alatus Roxb seedlings in the pot experiment. Malays. J. Microbiol. 2019, 15, 213–219. [Google Scholar] [CrossRef]
  134. Ravindran, R.; Hassan, S.S.; Williams, G.A.; Jaiswal, A.K. A review on bioconversion of agro-industrial wastes to industrially important enzymes. Bioengineering 2018, 5, 93. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  135. Giovannoni, M.; Gramegna, G.; Benedetti, M.; Mattei, B. Industrial use of cell wall degrading enzymes: The fine line between production strategy and economic feasibility. Front. Bioeng. Biotechnol. 2020, 8, 356. [Google Scholar] [CrossRef] [PubMed]
  136. Patil, P.P.; Prabhu, M.; Mutnuri, S. A novel and sustainable approach for biotransformation of phosphogypsum to calcium carbonate using urease producing Lysinibacillus sphaericus strain GUMP2. Environ. Technol. 2021, 5, 1–14. [Google Scholar] [CrossRef]
  137. Chakravarty, I.; Mandavgane, S.A. Valorization of fruit and vegetable waste for biofertilizer and biogas. J. Food Process Eng. 2021, 44, e13512. [Google Scholar] [CrossRef]
  138. Mishra, V.; Jana, A.K. Sweet sorghum bagasse pretreatment by Coriolus versicolor in mesh tray bioreactor for selective delignification and improved saccharification. Waste Biomass Valorization 2019, 10, 2689–2702. [Google Scholar] [CrossRef]
  139. Moreno-Bayona, D.A.; Gómez-Méndez, L.D.; Blanco-Vargas, A.; Castillo-Toro, A.; Herrera-Carlosama, L.; Poutou-Piñales, R.A.; Pedroza-Rodríguez, A.M. Simultaneous bioconversion of lignocellulosic residues and oxodegradable polyethylene by Pleurotus ostreatus for biochar production, enriched with phosphate solubilizing bacteria for agricultural use. PLoS ONE 2019, 14, e0217100. [Google Scholar]
  140. Silva, C.O.; Vaz, R.P.; Filho, E.X. Bringing plant cell wall-degrading enzymes into the lignocellulosic biorefinery concept. Biofuels Bioprod. Biorefining 2018, 12, 277–289. [Google Scholar]
  141. Fu, X.; Guo, Y.; Jin, Y.; Ma, M. Bioconversion of chitin waste using a cold-adapted chitinase to produce chitin oligosaccharides. Lwt 2020, 133, 109863. [Google Scholar] [CrossRef]
  142. Jayakumar, A.; Nair, I.C.; Radhakrishnan, E.K. Environmental adaptations of an extremely plant beneficial Bacillus subtilis Dcl1 identified through the genomic and metabolomic analysis. Microb. Ecol. 2021, 81, 687–702. [Google Scholar] [CrossRef] [PubMed]
  143. Banerjee, S.; Mandal, N.C. Diversity of chitinase-producing bacteria and their possible role in plant pest control. In Microbial Diversity in Ecosystem Sustainability and Biotechnological Applications; Springer: Singapore, 2019; pp. 457–491. [Google Scholar]
  144. Calin, M.; Raut, I.; Arsene, M.L.; Capra, L.; Gurban, A.M.; Doni, M.; Jecu, L. Applications of fungal strains with keratin-degrading and plant growth promoting characteristics. Agronomy 2019, 9, 543. [Google Scholar] [CrossRef]
  145. Tamreihao, K.; Mukherjee, S.; Khunjamayum, R.; Devi, L.J.; Asem, R.S.; Ningthoujam, D.S. Feather degradation by keratinolytic bacteria and biofertilizing potential for sustainable agricultural production. J. Basic Microbiol. 2019, 59, 4–13. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  146. Saeid, A. Phosphorus Microbial Solubilization as a Key for Phosphorus Recycling in Agriculture. In Phosphorus—Recovery and Recycling; Zhang, T., Ed.; IntechOpen: London, UK, 2018. [Google Scholar] [CrossRef] [Green Version]
  147. Saeid, A.; Labuda, M.; Chojnacka, K.; Górecki, H. Valorization of bones to liquid phosphorus fertilizer by microbial solubilization. Waste Biomass Valorization 2014, 5, 265–272. [Google Scholar] [CrossRef] [Green Version]
  148. Nandimath, A.P.; Karad, D.D.; Gupta, S.G.; Kharat, A.S. Consortium inoculum of five thermo-tolerant phosphate solubilizing Actinomycetes for multipurpose biofertilizer preparation. Iran. J. Microbiol. 2017, 9, 295. [Google Scholar] [PubMed]
  149. Santana, C.A.; Piccirillo, C.; Pereira, S.I.A.; Pullar, R.C.; Lima, S.M.; Castro, P.M.L. Employment of phosphate solubilising bacteria on fish scales–Turning food waste into an available phosphorus source. J. Environ. Chem. Eng. 2019, 7, 103403. [Google Scholar] [CrossRef]
  150. Busato, J.G.; Zandonadi, D.B.; Mól, A.R.; Souza, R.S.; Aguiar, K.P.; Júnior, F.B.R.; Olivares, F.L. Compost biofortification with diazotrophic and P-solubilizing bacteria improves maturation process and P availability. J. Sci. Food Agric. 2017, 97, 949–955. [Google Scholar] [CrossRef]
  151. Ortega-Torres, A.E.; Rico-García, E.; Guzmán-Cruz, R.; Torres-Pacheco, I.; Tovar-Pérez, E.G.; Guevara-González, R.G. Addition of Phosphatases and Phytases to Mature Compost to Increase Available Phosphorus: A Short Study. Agronomy 2021, 11, 2555. [Google Scholar] [CrossRef]
  152. O’Callaghan, M.; Ballard, R.A.; Wright, D. Soil microbial inoculants for sustainable agriculture: Limitations and opportunities. Soil Use Manag. 2022, 38, 1340–1369. [Google Scholar] [CrossRef]
  153. Devi, R.; Kaur, T.; Kour, D.; Yadav, A.; Yadav, A.N.; Suman, A.; Saxena, A.K. Minerals solubilizing and mobilizing microbiomes: A sustainable approach for managing minerals deficiency in agricultural soil. J. Appl. Microbiol. 2022, 133, 1245–1272. [Google Scholar] [CrossRef] [PubMed]
  154. Seneviratne, G.; Kecskés, M.L.; Kennedy, I.R. Biofilmed biofertilisers: Novel inoculants for efficient nutrient use in plants. ACIAR Proc. 2008, 130, 126–130. [Google Scholar]
  155. Rathnathilaka, T.; Premarathna, M.; Madawala, S.; Pathirana, A.; Karunaratne, K.; Seneviratne, G. Biofilm biofertilizer application rapidly increases soil quality and grain yield in large scale conventional rice cultivation: A case study. J. Plant Nutr. 2022, 2, 1–11. [Google Scholar] [CrossRef]
  156. Joulak, I.; Concórdio-Reis, P.; Torres, C.A.; Sevrin, C.; Grandfils, C.; Attia, H.; Azabou, S. Sustainable use of agro-industrial wastes as potential feedstocks for exopolysaccharide production by selected Halomonas strains. Environ. Sci. Pollut. Res. 2022, 29, 22043–22055. [Google Scholar] [CrossRef] [PubMed]
  157. Choi, I.S.; Ko, S.H.; Lee, M.E.; Kim, H.M.; Yang, J.E.; Jeong, S.G.; Park, H.W. Production, characterization, and antioxidant activities of an exopolysaccharide extracted from spent media wastewater after Leuconostoc mesenteroides WiKim32 fermentation. ACS Omega 2021, 6, 8171–8178. [Google Scholar] [CrossRef]
  158. Nazli, F.; Jamil, M.; Hussain, A.; Hussain, T. Exopolysaccharides and indole-3-acetic acid producing Bacillus safensis strain FN13 potential candidate for phytostabilization of heavy metals. Environ. Monit. Assess. 2020, 192, 1–16. [Google Scholar] [CrossRef]
  159. Marchetti, R.; Vasmara, C.; Fiume, F. Pig slurry improves the anaerobic digestion of waste cooking oil. Appl. Microbiol. Biotechnol. 2019, 103, 8267–8279. [Google Scholar] [CrossRef]
  160. Bialy, H.E.; Gomaa, O.M.; Azab, K.S. Conversion of oil waste to valuable fatty acids using oleaginous yeast. World J. Microbiol. Biotechnol. 2011, 27, 2791–2798. [Google Scholar] [CrossRef]
  161. Lam, M.K.; Lee, K.T.; Mohamed, A.R. Homogeneous, heterogeneous and enzymatic catalysis for transesterification of high free fatty acid oil (waste cooking oil) to biodiesel: A review. Biotechnol. Adv. 2010, 28, 500–518. [Google Scholar] [CrossRef]
  162. Zhou, B.; Zheng, X.; Zhu, Z.; Qin, Q.; Song, K.; Sun, L.; Xue, Y. Effects of fertilizer application on phthalate ester pollution and the soil microbial community in plastic-shed soil on long-term fertilizer experiment. Chemosphere 2022, 2, 136315. [Google Scholar] [CrossRef]
  163. Zhang, Y.; Liang, Q.; Gao, R.; Hou, H.; Tan, W.; He, X.; Wang, X. Contamination of phthalate esters (PAEs) in typical wastewater-irrigated agricultural soils in Hebei, North China. PLoS ONE 2015, 10, e0137998. [Google Scholar] [CrossRef] [PubMed]
  164. Zeng, F.; Cui, K.; Xie, Z.; Wu, L.; Liu, M.; Sun, G.; Zeng, Z. Phthalate esters (PAEs): Emerging organic contaminants in agricultural soils in peri-urban areas around Guangzhou, China. Environ. Pollut. 2008, 156, 425–434. [Google Scholar] [CrossRef] [PubMed]
  165. Wang, S.P.; Zhong, X.Z.; Wang, T.T.; Sun, Z.Y.; Tang, Y.Q.; Kida, K. Aerobic composting of distilled grain waste eluted from a Chinese spirit-making process: The effects of initial pH adjustment. Bioresour. Technol. 2017, 245, 778–785. [Google Scholar] [CrossRef] [PubMed]
  166. Huang, Y.L.; Sun, Z.Y.; Zhong, X.Z.; Wang, T.T.; Tan, L.; Tang, Y.Q.; Kida, K. Aerobic composting of digested residue eluted from dry methane fermentation to develop a zero-emission process. Waste Manag. 2017, 61, 206–212. [Google Scholar] [CrossRef]
  167. Luo, Y.; Wu, Y.; Wang, H.; Xing, R.; Zheng, Z.; Qiu, J.; Yang, L. Bacterial community structure and diversity responses to the direct revegetation of an artisanal zinc smelting slag after 5 years. Environ. Sci. Pollut. Res. 2018, 25, 14773–14788. [Google Scholar] [CrossRef]
  168. Chi, C.P.; Chu, S.; Wang, B.; Zhang, D.; Zhi, Y.; Yang, X.; Zhou, P. Dynamic bacterial assembly driven by Streptomyces griseorubens JSD-1 inoculants correspond to composting performance in swine manure and rice straw co-composting. Bioresour. Technol. 2020, 313, 123692. [Google Scholar] [CrossRef]
  169. Jiang, Y.; Dennehy, C.; Lawlor, P.G.; Hu, Z.; McCabe, M.; Cormican, P.; Gardiner, G.E. Exploring the roles of and interactions among microbes in dry co-digestion of food waste and pig manure using high-throughput 16S rRNA gene amplicon sequencing. Biotechnol. Biofuels 2019, 12, 1–16. [Google Scholar] [CrossRef] [Green Version]
  170. Jin, K.; Pezzuolo, A.; Gouda, S.G.; Jia, S.; Eraky, M.; Ran, Y.; Ai, P. Valorization of bio-fertilizer from anaerobic digestate through ammonia stripping process: A practical and sustainable approach towards circular economy. Environ. Technol. Innov. 2022, 27, 102414. [Google Scholar] [CrossRef]
  171. Santiago, B.; Moreira, M.T.; Feijoo, G.; González-García, S. Environmental comparison of banana waste valorisation strategies under a biorefinery approach. Waste Manag. 2022, 142, 77–87. [Google Scholar] [CrossRef]
  172. de Oliveira Gonçalves, M.; Carpanez, T.G.; Silva, J.B.G.; Otenio, M.H.; de Paula, V.R.; de Mendonça, H.V. Biomass Production of the Tropical Forage Grass Pennisetum purpureum (BRS Capiaçu) Following Biofertilizer Application. Waste Biomass Valorization 2022, 13, 2137–2147. [Google Scholar] [CrossRef]
  173. Gebremikael, M.T.; van Wickeren, N.; Salehi Hosseini, P.; De Neve, S. The impacts of black soldier fly frass on nitrogen availability, microbial activities, C sequestration, and plant growth. Front. Sustain. Food Syst. 2022, 6, 795950. [Google Scholar] [CrossRef]
  174. Green, B.W. Fertilizer use in aquaculture. In Feed and Feeding Practices in Aquaculture; Woodhead Publishing: Cambridge, MA, USA, 2022; pp. 29–63. [Google Scholar]
  175. Ibeto, C.N.; Lag-Brotons, A.J.; Marshall, R.; Semple, K.T. The nutritional effects of digested and undigested organic wastes combined with wood ash amendments on carrot plants. J. Soil Sci. Plant Nutr. 2020, 20, 460–472. [Google Scholar] [CrossRef]
  176. Hidaka, T.; Nakamura, M.; Oritate, F.; Nishimura, F. Utilization of high solid waste activated sludge from small facilities by anaerobic digestion and application as fertilizer. Water Sci. Technol. 2019, 80, 2320–2327. [Google Scholar] [CrossRef] [PubMed]
  177. Schardt, C.; Adams, M.B.; Owens, T.; Keitz, S.; Fontelo, P. Utilization of the PICO framework to improve searching PubMed for clinical questions. BMC Med. Inform. Decis. Mak. 2007, 7, 1–6. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  178. Azeem, M.; Hassan, T.U.; Tahir, M.I.; Ali, A.; Jeyasundar, P.G.S.A.; Hussain, Q.; Zhang, Z. Tea leaves biochar as a carrier of Bacillus cereus improves the soil function and crop productivity. Appl. Soil Ecol. 2021, 157, 103732. [Google Scholar] [CrossRef]
  179. Ajeng, A.A.; Abdullah, R.; Ling, T.C.; Ismail, S.; Lau, B.F.; Ong, H.C.; Chang, J.S. Bioformulation of biochar as a potential inoculant carrier for sustainable agriculture. Environ. Technol. Innov. 2020, 20, 101168. [Google Scholar] [CrossRef]
Figure 1. Schematic representation of the inclusion and exclusion criteria utilized in this study.
Figure 1. Schematic representation of the inclusion and exclusion criteria utilized in this study.
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Figure 2. PRISMA flowchart reporting the article selection process for the systematic literature review.
Figure 2. PRISMA flowchart reporting the article selection process for the systematic literature review.
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Figure 3. Geographical distribution of bioconversion research during the last five years (2017–2022).
Figure 3. Geographical distribution of bioconversion research during the last five years (2017–2022).
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Figure 4. Trends in research publication using the keywords “waste valorisation”, “bioconversion” and “biofertilizer” over time.
Figure 4. Trends in research publication using the keywords “waste valorisation”, “bioconversion” and “biofertilizer” over time.
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Figure 5. Graphical representation of co-occurrence mapping of relevant keywords associated with fertilizer research.
Figure 5. Graphical representation of co-occurrence mapping of relevant keywords associated with fertilizer research.
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Figure 6. Visualisation of critical terms co-occurrence in textual data used in fertilizer research.
Figure 6. Visualisation of critical terms co-occurrence in textual data used in fertilizer research.
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Figure 7. Depicting the co-authorship between countries that engage in intensive fertilizer-based research and their citation weightage.
Figure 7. Depicting the co-authorship between countries that engage in intensive fertilizer-based research and their citation weightage.
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Figure 8. Tracking the journals that are involved in intensive fertilizer-based research and their relative impact factor.
Figure 8. Tracking the journals that are involved in intensive fertilizer-based research and their relative impact factor.
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Table 1. Search strategy used to retrieve relevant research articles.
Table 1. Search strategy used to retrieve relevant research articles.
Search StrategyScopusWeb of Science
biofertilizer * AND waste * AND fung *5664
biofertilizer * AND waste * AND bacteria *109121
“Plant growth” AND waste * AND bacteria *449461
“Plant growth” AND waste * AND fung *202217
fertilizer AND waste AND fungi148154
fertilizer AND waste AND bacteria632412
biofertilizer AND waste298252
biofertilizer AND bacteria606507
biofertilizer AND fungi268252
bioconversion AND waste AND fungi12799
bioconversion AND waste AND bacteria469203
bioinoculant * AND waste *1119
Year range was limited to 2017–2021 (last five years)
“*” indicates the truncated version of the term (fung * represents fungus, fungi, fungal) as recognised by the search algorithm.
Table 2. PICO framework utilization for the development of the research question.
Table 2. PICO framework utilization for the development of the research question.
Problem (P)Extensive Use of Chemical Fertilizers
Intervention (I)application of biofertilizers produced by the waste valorization
Comparison (C)different types of microbial inoculants used for waste valorization for biofertilizer production
Outcome (O)Identification of microbial inoculants with potential and used for wastes bioconversion strategies
Table 3. Inclusion and exclusion criteria used in this study.
Table 3. Inclusion and exclusion criteria used in this study.
Inclusion CriteriaExclusion Criteria
Studies that used plant growth studies in pot, or plot settingsReview articles associated with anaerobic digestion or composting
Articles published during 2017–2021Studies that were related to waste pre-treatment techniques, biorefinery, microalgae production
Studies that studied microbial inoculants for the bioconversion of wastes into fertilizers only on plate-based or culture-based setups without plant growth assessments
Studies that assessed microbial inoculants for the bioconversion of wastes into fertilizersConference proceedings and posters were excluded
Table 4. Some of the terms allocated into clusters based on mapping of textual data.
Table 4. Some of the terms allocated into clusters based on mapping of textual data.
Parameters of Interest in
Fertilizer Studies
Plant Growth Promoting MicroorganismsKeywords in
Circular Economy
Parameters of Plant Growth Promotion by Microorganisms
Ash, soil amendment, Biofertilizer treatment, Carrier material, seed inoculation, co-inoculation, chlorophyll content, available p, bacterial community, abundance, field experiment, root, shoot, dry and fresh weight, urea, greenhouse experiment, crop yield, harvest, growth parameters, NPK, nutrient content and uptake, Oryza sativa, Triticum aestivum, soybeanBacillus subtilis, Burkholderia, Fusarium oxysporum, Enterobacter, Azotobacter chroococcum, Bacillus megaterium, endophytic bacterium, solubilizing bacteria, Trichoderma, Pseudomonas, Rhizobium, rhizobacteria, SerratiaAgricultural waste, anaerobic digestion, biochar, biofuel, biogas, composting, circular economy, feedstock, digestate, electricity, energy, environmental impact, recovery, recycling, reduction, industry, pollution, sustainable development, circular economy, waste valorization, wastewater, food waste, sewage sludgeACC deaminase, acetic acid, ammonia, biocontrol, biopesticide, catalase, protease, chitinase, IAA production, nitrogen fixation, phosphate solubilization, phytohormone, salt stress, seedling germination, siderophore and gibberellic acid production
Table 5. Different types of consortia used for bioconversion of wastes.
Table 5. Different types of consortia used for bioconversion of wastes.
Inoculum TypeType of MicroorganismMicrobial Inoculant UsedWaste UsedReference
consortiaactinomycetesActinomycetessawdust plus chicken litter[34]
consortiabacteriaAeromonas, Bacillus, Thaueraamino aromatica, Acinetobacter (a consortium of 7 isolates)Dairy Wastewater[24]
consortiabacteriacellulolytic bacterial consortiumorganic liquid waste (rice washing, coconut water liquid, tofu liquid waste, and palm oil mill liquid waste)[35]
consortiabacteriaconsortium of decomposer microorganisms: Bacillus pumilus AL16, Microbacterium terregens AC1180, Aeromonas sp. B5376, Arthrobacter globiformis AC1529, Streptomyces olivocinereus AC1169 and Acinetobacter sp. B390.feather-downy waste and dung[28]
consortiabacterialactic acid bacteriasilage (BE) of shrimp head, molasses, and milk[36]
consortiacyanobacteriacyanobacteria (Fischerella muscicola, Anabaena variabilis, Aulosira fertilissima, Tolypothrix tenuis)Chilli waste (stems and leaves after harvesting the fruit)[37]
consortiacyanobacteriaChlorella sp., Dictyosphaerium sp., Monoraphidium sp., Neochloris sp. and Scenedesmus sp.municipal wastewater (MWW) with simulated flue gas[38]
consortiamixedEnhydrobacter aerosaccus (ACCA2 JX042472), Aspergillus sp. (ALUH KT356201)raw rice husk (RRH)[39]
consortiamixedAcidithiobacillus, Beijerinckia indica and Cunninghamella elegansrock biofertilizers mixed with sulfur[27]
consortiaunknownEM bokashipetroleum sludge[40]
Table 6. Table of evidence (ToE) matrix constructed based on systematic literature review of 74 research articles.
Table 6. Table of evidence (ToE) matrix constructed based on systematic literature review of 74 research articles.
Waste UsedBioconversion StrategyMicrobial Inoculant UsedPlant TestedMode of ApplicationType of Test (In Vitro/Pot/Plot)Role of MicrobeReferences
Cattle hooves (slaughterhouse waste)submerged fermentationLichtheimia corymbifera AS1Vigna mungoirrigation with hydrolysed hoovesgermination and pot testskeratinolysis[41]
Olive mill solid waste (OMSW)fermentationAspergillus tamariiVicia fabasoil amendmentgermination and pot testsfermentation[42]
petroleum sludgebiodegradationEM bokashiOnionsoil amendmentpot testsbiodegradation[40]
Municipal solid wastes (MSW)compostingStreptomyces sp. Al-Dhabi 30Solanum lycopersicumsoil amendmentgermination and pot testsplant growth promotion (IAA, siderophore, phosphate solubilization), hydrolytic enzyme production (cellulase, pectinase), biocontrol[43]
Municipal organic wastescompostingPenicillium vinaceum and Eupenicillium hirayamaCapsicum annuum (pepper), Solanum melongena (aubergine) and S. lycopersicum (tomato)soil supplementationplot testsplant growth promotion, biocontrol[44]
Mixture of sawdust, sewage sludge, chicken littercompostingActinomycetes (thermo-tolerant)Okra (Albenus Esculentus) and Maize (Zea-mays)soil amendmentplot testsfermentation, nitrogen fixation[34]
composite of sawdust, chicken litter, vegetable waste, sewage sludgecompostingStreptomyces spp and Rothia sppOkra (Albenus Esculentus) and Maize (Zea-mays)soil amendmentplot testscellulolytic, ligninolytic, nitrogen mineralization[45]
jarosite wastenanoparticle synthesisAspergillus terreus strain J4Triticum aestivumseed priminggermination testsbioleaching[46]
Dairy Wastewaterbiofilm bioreactorAeromonas, Bacillus, Thaueraamino aromatica, Acinetobacter (consortium of 7 isolates)Mung bean (var. Meha)soil irrigationplot testsbiofilm production[24]
Chicken featherssubmerged fermentationBacillus cereustomatosoil amendmentplot testskeratinolysis[47]
1% (w/w) keratin wastes (chicken feathers and sheep wool)preparation of Protein Hydrolysates (PHs)Trichoderma asperellumSolanum lycopersicumweekly application of PHSgermination and pot testsplant growth promotion (IAA production, siderophore, cellulase activity, phosphate solubilization), biocontrol[48]
fruit pulp from of ripened fruits not suitable for human consumptionsubmerged fermentation (culture medium)Komagataeibacter medellinensisOnionsoil amendmentpot testsproduction of Bacterial Nanocellulose Mulch[49]
Mixture of Cattle manure organic fertilizer (composted) and biocharfermentationArthrobacter sp. DNS10soybeansoil amendmentgermination and pot tests[50]
Chilli waste (stems and leaves after harvesting the fruit)microbial enrichmentcyanobacteria (Fischerella muscicola, Anabaena variabilis, Aulosira fertilissima, Tolypothrix tenuis)Brinjal (Solanum melongena)soil amendmentpot testsnutrient recovery[37]
municipal wastewater (MWW) with simulated flue gasmicro-algal biorefinery approachChlorella sp., Dictyosphaerium sp., Monoraphidium sp., Neochloris sp. and Scenedesmus sp.Wheatsoil supplementationGermination testnutrient recovery[38]
Mixed medicinal plant wastecompostingconsortia of Streptomyces, Paenibacillus, Bacillus and HymenobacterFagopirum esculentum, Thymus vulgaris, Cynara scolimus and Lavandula officinalisseed priminggermination testsplant growth promotion[51]
combination of rice washing water waste, tofu liquid waste, coconut water waste, and palm oil liquid wasteIncubation of liquid waste with bacterial consortium for 21 days (fermentation)Bacillus cereus JP6, Bacillus cereus JP7, Proteus mirabilis TKKS3, Proteus mirabilis TKKS7, Providencia vermicola SA1 and Bacillus cereus SA6upland rice (Oryza sativa L.)soil amendmentplot testscellulolysis, fermentation[35]
Spent coffee grounds (SCG), poultry manure, and agricultural waste-derived biocharcompostingStreptomyces albus, Gibellulopsis nigrescens, Bacillus licheniformis, Bacillus smithii, and Alternaria tenuissima.pepper and leeksoil amendmentgermination and pot testsmicrobial bioaugmentation[52]
sewage sludge and agricultural wastecompostingBacillus megateriumChinese flowering cabbagepolluted soil supplementationplot testsPAEs degradation and phosphate solubilization[53]
brewery wastewater (BWW)micro-algal biorefinery approachScenedesmus obliquus (ACOI 204/07)barley and wheat seedssoil supplementationgermination and pot testsnutrient recovery[54]
cane bagasse and broadbean seed capsule compositesolid-state fermentation (SSF)Kosakonia cowanii LT-1Zea mays L.soil amendmentpot testsEPS production[55]
feather waste (FW) and coconut oil cake (COC)Biorefinery-FermentationHaloferax lucentensis GUBF-2 MG076878Oryza sativa L. var. Korgutseed priming, soil amendmentgermination and pot testsproduction of protease and lipase haloextremozymes, Feather and COC Hydrolysate[56]
biological silage (BE) of shrimp head, molasses and milkfermentationlactic acid bacteriamaralfalfa grassapplication of leachateplot testsproduction of fermented liquid fertilizer[36]
sugarcane molassesfermentationCorynebacterium glutamicumBrassica campestris var. Pekinensisfoliar applications of fermented brothpot testsfermentation[57]
wastewater from a WWTPsolid-state formulationsScenedesmus sp.Ryegrass and (b) barleysoil application of lyophilised microalgae with vegetable compostplot testsnutrient recovery[58]
pressmudsolid state fermentationBacillus circulansjowar and bajrasoil amendmentplot testsfermentation and phosphate solubilization[59]
native chicken feathersfermentationChryseobacterium sp. RBTSolanum melongena L and Capsicum annuum L.foliar spray (S 5%, v/v) and root drenching (RD) (20%, v/v)pot and plot testsKeratinase[60]
sardine waste (SW), potato peels (PP), and poultry waste (PW)mesophilic bio-digestionAspergillus niger and Saccharomyces cerevisiaebell pepperssoil amendmentseed germination and pot testsfermentation[61]
Vermicompost and lignite (carrier)fermentationAzospirillum lipoferum (Az 204), Bacillus
megaterium (PB2) and Pseudomonas
fluorescens(Pf1)
upland rice NLR 145 (Oryza sativa L.)soil supplementationpot testscellulolysis[62]
coconut fibremedium for mass micropropagule productionTrichoderma asperellum B1092Cherry tomato var. Sakura 318soil amendmentpot testsbiocontrol against Fusarium oxysporum f. sp. lycopersici B713T[63]
A. bisporus industrial wastewatersubmerged fermentation (culture medium)Bacillus cereusBrassica chinensis LApplication of treated liquid fermentation broth at proper intervalsplot testsfermentation[64]
(ZnO)-orange peel waste compositebio-activationBacillus sp. AZ6Zea mays L.soil amendmentplot testszinc solubilization[65]
Lobster processing wastesSubmerged fermentationStreptomyces griseusArabidopsis thalianafoliar applications of extractsgermination testschitinolysis, biocontrol[66]
lignocellulosic green waste (GW) from Municipal solid waste (MSW)compostingAspergillus fumigatus and Geotrichum sp.Capsicum annuum L.soil amendmentpot testscellulolytic and ligninolytic decomposer inducer[67]
WWTP ash and poultry bone wastesgranulation and microbiological activationBacillus megaterium and Acidithiobacillus ferrooxidansWheatsoil supplementationPhytotoxicity seed germination testphosphate solubilization[25]
sewage sludge ash and dried animal (porcine) bloodbiological activation and granulationBacillus megateriumwheat (Triticum aestivum ssp. vulgare MacKey)soil amendmentpot testsphosphate solubilization[68]
sewage sludge ash and animal bonesenrichment and granulationBacillus megaterium and Acidithiobacillus ferrooxidanswinter wheatsoil supplementationplot testsphosphate solubilization[29]
chicken featherscompostingChrysosporium indicum JK14Zea mays L.soil amendmentpot testskeratinolysis[69]
Chicken feather wastesubmerged state fermentationAlternaria tenuissimaChickpea (Cicer arietinum)soil supplementationplot testskeratinolysis[70]
kitchen waste oilfermentationPseudomonas aeruginosa ATC 15442Cabbagedrip irrigationpot testslong chain triglycerides (LCTs) degradation[71]
spent mushroom substrate (SMS) compostsemi-solid fermentationPantoea agglomerans ZBChili pepper seedlingssoil supplementationplot testsphosphate solubilization[72]
sugarcane filter cake and boiler ashcompostingconsortia of Pseudomonas aeruginosa PSBR12, Bacillus sp. BACBR04, Bacillus sp. BACBR06, Bacillus sp. BACBR01 and Rhizobium sp. RIZBR01sugarcanesoil amendmentplot testsphosphate solubilization[73]
low-moisture food waste materialcompostingAspergillus niger UY2015_11Lactuca sativa var. crispa (lettuce), and Brassica rapa var. perviridissoil supplementationphytotoxicity and plot testsnitrogen release, phosphate solubilization[74]
raw press mudcompostingAspergillus niger (RHS/M492-NAIMCC-F-02890)Zea mays L.soil amendmentplot testsphosphate and zinc solubilization[75]
chicken featherscompostingBacillus subtilis FW12green gramsoil amendmentpot testskeratinolysis[76]
kitchen waste (79%), chita-dhan (unfilled rice grain) biochar (15%), rock phosphate (5%)co-compostinga consortium of 10 PGPB (1%) (Bacillus mycoides, Proteus sp., Bacillus cereus, Bacillus subtilis, Bacillus pumilus, Paenibacillus polymyxa, and Paenibacillus spp.)Oryza sativa Lfertilizer amendmentplot testsplant growth promotion (IAA production, phosphate solubilization, N2 fixation)[77]
Glycerin pitchfermentationLactobacillus spp.cucumbersoil supplementationpot testsglycerin biodegradation[78]
domestic wastewater from wastewater sewage pump with coal-fired flue gas (2.5% CO2)microalgae cultivation and lipid extractionScenedesmus sp.Oryza sativasoil amendmentpot testsnutrient recovery[79]
organic vegetable heapscompostingClonostachys rosea f. catenulaSolanum lycopersicumsoil amendmentpot testsbiocontrol, plant growth promotion[80]
natural phosphate and potash rockphosphate solubilization pilesAcidithiobacillus thiooxidans, Beijerinckia indicaSugarcanesoil supplementationplot testsphosphate solubilization[81]
Crustacean shell waste (shrimp and crab shell powder (SCSP))Submerged fermentationAlcaligenes faecalis SK10Pisum sativum and Cicer arietinumsoil amendmentpot testschitinolysis and proteolysis[82]
vermicompostmicrobial enrichmentconsortia of Serratia marcescens, Pseudomonas aeruginosa, and Bacillus cereustomato and wheatsoil amendmentpot testsphosphate solubilization[83]
vineyard wastecompostingTrichoderma harzianum T-78muskmelonsoil supplementationpot testsplant growth promotion, biocontrol[84]
organic biomedical wasteanerobic fermentation followed by incinerationPasterulla canis circinelloidesSolanum lycopersicumsoil amendmentpot testsplant nutrient dynamics, biodegradation[85]
mixture of feather-downy waste and dung (8 : 2)biohumus production through decompositionconsortium of decomposer microorganisms: Bacillus pumilus AL16, Microbacterium terregens AC1180, Aeromonas sp. B5376, Arthrobacter globiformis AC1529, Streptomyces olivocinereus AC1169 and Acinetobacter sp. B390winter wheat cropssoil amendmentplot testsdecomposition[28]
sewage sludge ashesfungal spore inoculation for 8 daysPenicillium bilaiae DBS-5 and Aspergillus niger ATCC 9142spring wheat (Triticum aestivum L. cv. Dacke)soil applicationplot testsphosphate solubilization[86]
sugarcane molassesfermentationCorynebacterium glutamicumPotatofoliar applicationplot testsglutamic acid production[87]
sewage sludge ash and spent mushroom substratesolid-state solubilization and compostingAcidithiobacillus ferrooxidanssunflower seedssoil amendmentgermination testsphosphate solubilization[88]
Spent Coffee Grounds, Rice Bran, and BiocharcompostingBacillus sp. and Actinomyces sp.pepper and leeksoil amendmentpot testsplant growth, biocontrol[89]
biogas residue, rice straw and cattle manurecompostingStreptomyces microflavus G33Solanum lycopersicumsoil amendmentplot testsbiocontrol[90]
domestic wastewatermicroalgae cultivation and lipid extractionChlorella sp. (KP972095) and Scenedesmus sp. (KR025877)Solanum lycopersicumsoil amendmentpot testsnutrient recovery[91]
spent mushroom substrate (SMS)fungal digestionTrichoderma harzianumSolanum lycopersicumsoil amendmentpot testsmycodegradation[92]
rock biofertilizers mixed with sulfurcompostingAcidithiobacillus, Beijerinckia indica and Cunninghamella elegansbanana “Williams”soil supplementationplot testsphosphate solubilization[27]
rice strawsolid-state fermentation (SSF)Aspergillus niger (RHS/M492-NAIMCC-F-02890)Oryza sativa Lseedling spraygermination and pot testsproduction of fungal-based chitosan[93]
black water (toilet wastewater)micro-algal biorefinery approachChlorella sorokinianaspring barley (Hordeum vulgare L.)soil supplementationPhytotoxicity seed germination test and plot testsnutrient recovery[94]
Chicken feathers powderLiquid FermentationBacillus pumilus JYLwheatsoil supplementationpot testskeratinolysis[95]
rice husk (RH)compostingAspergillus spblack gramsoil amendmentpot testscellulolytic activity[39]
paddy-soaked rice mill wastewater (PSRMW)micro-algal biorefinery approachChlorella pyrenoidosaIndian okra (Abelmoschus angulosus)soil amendmentpot testsnutrient recovery[96]
lignin wastefermentationMeyerozyma guilliermondii and Providencia rettgeriCowpeafoliar applicationSeed germination pot testsligninolysis[97]
chicken manurefermentationBacillus subtilisChinese cabbage and rape seedsseed immersiongermination and pot testsdecomposition[26]
duck featherscompostingconsortia of Arthrobacter ureafaciens K10 and Streptomyces sp. CP3cherry tomatoseed priminggermination and pot testsfeather degradation, phosphatesolubilization, and IAA formation[98]
Cow Manure and rapeseed mealSolid State FermentationBacillus sp. XG-1Citrullus lanatus Thumb.soil amendmentplot testsplant growth promotion (IAA, gibberellins, phytase), biocontrol[99]
prickly ash seeds (PAS) and biochar from rice huskssolid state fermentationBacillus subtilis Tpb55rape seedsseed immersion and soil amendmentgermination and pot testsbiocontrol[100]
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Kiruba N, J.M.; Saeid, A. An Insight into Microbial Inoculants for Bioconversion of Waste Biomass into Sustainable “Bio-Organic” Fertilizers: A Bibliometric Analysis and Systematic Literature Review. Int. J. Mol. Sci. 2022, 23, 13049. https://doi.org/10.3390/ijms232113049

AMA Style

Kiruba N JM, Saeid A. An Insight into Microbial Inoculants for Bioconversion of Waste Biomass into Sustainable “Bio-Organic” Fertilizers: A Bibliometric Analysis and Systematic Literature Review. International Journal of Molecular Sciences. 2022; 23(21):13049. https://doi.org/10.3390/ijms232113049

Chicago/Turabian Style

Kiruba N, Jennifer Michellin, and Agnieszka Saeid. 2022. "An Insight into Microbial Inoculants for Bioconversion of Waste Biomass into Sustainable “Bio-Organic” Fertilizers: A Bibliometric Analysis and Systematic Literature Review" International Journal of Molecular Sciences 23, no. 21: 13049. https://doi.org/10.3390/ijms232113049

APA Style

Kiruba N, J. M., & Saeid, A. (2022). An Insight into Microbial Inoculants for Bioconversion of Waste Biomass into Sustainable “Bio-Organic” Fertilizers: A Bibliometric Analysis and Systematic Literature Review. International Journal of Molecular Sciences, 23(21), 13049. https://doi.org/10.3390/ijms232113049

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