Potentials of Endophytic Fungi in the Biosynthesis of Versatile Secondary Metabolites and Enzymes
Abstract
:1. Introduction
2. Endophyte–Host Plant Interactions
3. Processes of Isolation and Characterization of Endophytic Fungi
4. History of Fungal Production of Secondary Metabolites
5. Processes of Fungal Secondary Metabolite Production
6. Biotechnological Applications of Secondary Metabolites Produced by Endophytic Fungi
6.1. Medicinal and Pharmaceutical Applications
6.2. Agricultural Applications
6.3. Industrial Applications
6.4. Bioremediation Applications
7. Challenges and Solutions to Improve Secondary Metabolite Discovery
8. Conclusions
Supplementary Materials
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Conflicts of Interest
References
- Ayukekbong, J.A.; Ntemgwa, M.; Atabe, A.N. The threat of antimicrobial resistance in developing countries: Causes and control strategies. Antimicrob. Resist. Infect. Control 2017, 6, 47. [Google Scholar] [CrossRef]
- Vasan, N.; Baselga, J.; Hyman, D.M. A view on drug resistance in cancer. Nature 2019, 575, 299–309. [Google Scholar] [CrossRef] [Green Version]
- Venugopalan, A.; Srivastava, S. Endophytes as in vitro production platforms of high value plant secondary metabolites. Biotechnol. Adv. 2015, 33, 873–887. [Google Scholar] [CrossRef]
- Aharwal, R.P.; Kumar, S.; Sandhu, S.S. Endophytic mycoflora as a source of biotherapeutic compounds for disease treatment. J. Appl. Pharm. Sci. 2016, 6, 242–254. [Google Scholar] [CrossRef] [Green Version]
- Khare, E.; Mishra, J.; Arora, N.K. Multifaceted interactions between endophytes and plant: Developments and prospects. Front. Microbiol. 2018, 9, 2732. [Google Scholar] [CrossRef] [PubMed]
- Li, F.-S.; Weng, J.-K. Demystifying traditional herbal medicine with modern approach. Nat. Plants 2017, 3, 17019. [Google Scholar] [CrossRef] [PubMed]
- Othman, L.; Sleiman, A.; Abdel-Massih, R.M. Antimicrobial activity of polyphenols and alkaloids in Middle Eastern plants. Front. Microbiol. 2019, 10, 911. [Google Scholar] [CrossRef] [PubMed]
- Zeilinger, S.; Gupta, V.K.; Dahms, T.E.S.; Silva, R.N.; Singh, H.B.; Upadhyay, R.S.; Gomes, E.V.; Tsui, C.K.-M.; Nayak, S.C. Friends or foes? Emerging insights from fungal interactions with plants. FEMS Microbiol. Rev. 2016, 40, 182–207. [Google Scholar] [CrossRef] [Green Version]
- Yan, L.; Zhao, H.; Zhao, X.; Xu, X.; Di, Y.; Jiang, C.; Shi, J.; Shao, D.; Huang, Q.; Yang, H.; et al. Production of bioproducts by endophytic fungi: Chemical ecology, biotechnological applications, bottlenecks, and solutions. Appl. Microbiol. Biotechnol. 2018, 102, 6279–6298. [Google Scholar] [CrossRef]
- Omomowo, O.I.; Babalola, O.O. Bacterial and fungal endophytes: Tiny giants with immense beneficial potential for plant growth and sustainable agricultural productivity. Microorganisms 2019, 7, 481. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Gupta, S.; Chaturvedi, P.; Kulkarni, M.G.; Van Staden, J. A critical review on exploiting the pharmaceutical potential of plant endophytic fungi. Biotechnol. Adv. 2020, 39, 107462. [Google Scholar] [CrossRef]
- Slama, H.; Cherif-Silini, H.; Chenari Bouket, A.; Qader, M.; Silini, A.; Yahiaoui, B.; Alenezi, F.N.; Luptakova, L.; Triki, M.A.; Vallat, A.; et al. Screening for Fusarium antagonistic bacteria from contrasting niches designated the endophyte Bacillus halotolerans as plant warden against Fusarium. Front. Microbiol. 2019, 9, 3236. [Google Scholar] [CrossRef] [Green Version]
- Slama, H.; Triki, M.; Chenari Bouket, A.; Mefteh, F.B.; Alenezi, F.N.; Luptakova, L.; Cherif-Silini, H.; Vallat, A.; Oszako, T.; Gharsallah, N.; et al. Screening of the high-rhizosphere competent Limoniastrum monopetalum’ culturable endophyte microbiota allows the recovery of multifaceted and versatile biocontrol agents. Microorganisms 2019, 7, 249. [Google Scholar] [CrossRef] [Green Version]
- Kusari, S.; Hertweck, C.; Spiteller, M. Chemical ecology of endophytic fungi: Origins of secondary metabolites. Chem. Biol. 2012, 19, 792–798. [Google Scholar] [CrossRef] [Green Version]
- Hiruma, K.; Kobae, Y.; Toju, H. Beneficial associations between Brassicaceae plants and fungal endophytes under nutrient-limiting conditions: Evolutionary origins and host-symbiont molecular mechanisms. Curr. Opin. Plant Biol. 2018, 44, 145–154. [Google Scholar] [CrossRef] [PubMed]
- Fadiji, A.E.; Babalola, O.O. Elucidating mechanisms of endophytes used in plant protection and other bioactivities with multifunctional prospects. Front. Bioeng. Biotechnol. 2020, 8, 467. [Google Scholar] [CrossRef] [PubMed]
- Slama, H.; Cherif-Silini, H.; Chenari Bouket, A.; Silini, A.; Alenezi, F.N.; Luptakova, L.; Vallat, A.; Belbahri, L. Biotechnology and bioinformatics of endophytes in biocontrol, bioremediation, and plant growth promotion. In Endophytes: Mineral Nutrient Management, Volume 3. Sustainable Development and Biodiversity; Maheshwari, D.K., Dheeman, S., Eds.; Springer: Cham, Switzerland, 2021; Volume 26, pp. 181–205. [Google Scholar] [CrossRef]
- Rana, K.L.; Kour, D.; Kaur, T.; Devi, R.; Negi, C.; Yadav, A.N.; Yadav, N.; Singh, K.; Anil Kumar Saxena, A.K. Endophytic fungi from medicinal plants: Biodiversity and biotechnological applications. In Microbial Endophytes, Functional Biology and Applications; Kumar, A., Radhakrishnan, E.K., Eds.; Elsevier: Amsterdam, The Netherlands, 2020; pp. 273–305. [Google Scholar]
- Hawksworth, D.L.; Lücking, R. Fungal diversity revisited: 2.2 to 3.8 million species. In The Fungal Kingdom; Heitman, J., Howlett, B.J., Crous, P.W., Stukenbrock, E.H., James, T.Y., Gow, N.A.R., Eds.; ASM Press: Washington, DC, USA, 2017; pp. 79–95. [Google Scholar] [CrossRef]
- Manganyi, M.C.; Ateba, C.N. Untapped potentials of endophytic fungi: A review of novel bioactive compounds with biological applications. Microorganisms 2020, 8, 1934. [Google Scholar] [CrossRef]
- Obermeier, M.-M.; Christina, A. Prospects for biotechnological exploitation of endophytes using functional metagenomics. In Endophyte Biotechnology: Potential for Agriculture and Pharmacology, 1st ed.; Shouten, A., Ed.; CABI: Wallingford, UK, 2019; pp. 164–179. [Google Scholar]
- Rustamova, N.; Wubulikasimu, A.; Mukhamedov, N.; Gao, Y.; Egamberdieva, D.; Yili, A. Endophytic bacteria associated with medicinal plant Vernonia anthelmintica: Diversity and characterization. Curr. Microbiol. 2020, 77, 1457–1465. [Google Scholar] [CrossRef] [PubMed]
- Keller, N.P. Fungal secondary metabolism: Regulation, function and drug discovery. Nat. Rev. Microbiol. 2019, 17, 167–180. [Google Scholar] [CrossRef]
- Vasundhara, M.; Reddy, M.S.; Kumar, A. Secondary metabolites from endophytic fungi and their biological activities. In New and Future Developments in Microbial Biotechnology and Bioengineering; Gupta, V.K., Pandey, A., Eds.; Elsevier: Amsterdam, The Netherlands, 2019; pp. 237–258. [Google Scholar] [CrossRef]
- Torres-Mendoza, D.; Ortega, H.E.; Cubilla-Rios, L. Patents on endophytic fungi related to secondary metabolites and biotransformation applications. J. Fungi 2020, 6, 58. [Google Scholar] [CrossRef]
- Mandal, S.; Banerjee, D. Proteases from endophytic fungi with potential industrial applications. In Recent Advancement in White Biotechnology Through Fungi. Fungal Biology; Yadav, A., Mishra, S., Singh, S., Gupta, A., Eds.; Springer: Cham, Switzerland, 2019; pp. 319–359. [Google Scholar] [CrossRef]
- Rana, K.L.; Kour, D.; Sheikh, I.; Dhiman, A.; Yadav, N.; Yadav, A.N.; Rastegari, A.A.; Singh, K.; Saxena, A.K. Endophytic fungi: Biodiversity, ecological significance, and potential industrial applications. In Recent Advancement in White Biotechnology Through Fungi: Volume 1: Diversity and Enzymes Perspectives Fungal Biology; Yadav, A.N., Mishra, S., Singh, S., Gupta, A., Eds.; Springer: Cham, Switzerland, 2019; pp. 1–62. [Google Scholar] [CrossRef]
- Field, K.J.; Pressel, S.; Duckett, J.G.; Rimington, W.R.; Bidartondo, M.I. Symbiotic options for the conquest of land. Trends Ecol. Evol. 2015, 30, 477–486. [Google Scholar] [CrossRef] [PubMed]
- Wani, Z.A.; Ashraf, N.; Mohiuddin, T.; Riyaz-Ul-Hassan, S. Plant-endophyte symbiosis, an ecological perspective. Appl. Microbiol. Biotechnol. 2015, 99, 2955–2965. [Google Scholar] [CrossRef]
- Martinez-Klimova, E.; Rodríguez-Peña, K.; Sánchez, S. Endophytes as sources of antibiotics. Biochem. Pharmacol. 2017, 134, 1–17. [Google Scholar] [CrossRef]
- Rabiey, M.; Hailey, L.E.; Roy, S.R.; Grenz, K.; Al-Zadjali, M.A.S.; Barrett, G.A.; Jackson, R.W. Endophytes vs. tree pathogens and pests: Can they be used as biological control agents to improve tree health? Eur. J. Plant Pathol. 2019, 155, 711–729. [Google Scholar] [CrossRef] [Green Version]
- Wang, L.; Ren, L.; Li, C.; Gao, C.; Liu, X.; Wang, M.; Luo, Y. Effects of endophytic fungi diversity in different coniferous species on the colonization of Sirex noctilio (Hymenoptera: Siricidae). Sci. Rep. 2019, 9, 5077. [Google Scholar] [CrossRef]
- Slama, H.B.; Chenari Bouket, A.; Alenezi, F.N.; Khardani, A.; Luptakova, L.; Vallat, A.; Oszako, T.; Rateb, M.E.; Belbahri, L. Olive mill and olive pomace evaporation pond’s by-products: Toxic level determination and role of indigenous microbiota in toxicity alleviation. Appl. Sci. 2021, 11, 5131. [Google Scholar] [CrossRef]
- Balla, A.; Silini, A.; Cherif-Silini, H.; Chenari Bouket, A.; Moser, W.K.; Nowakowska, J.A.; Oszako, T.; Benia, F.; Belbahri, L. The Threat of Pests and Pathogens and the Potential for Biological Control in Forest Ecosystems. Forests 2021, 12, 1579. [Google Scholar] [CrossRef]
- Delaye, L.; García-Guzmán, G.; Heil, M. Endophytes versus biotrophic and necrotrophic pathogens—are fungal lifestyles evolutionarily stable traits? Fungal Divers. 2013, 60, 125–135. [Google Scholar] [CrossRef]
- Newman, D.J.; Cragg, G.M. Natural products as sources of new drugs over the nearly four decades from 01/1981 to 09/2019. J. Nat. Prod. 2020, 83, 770–803. [Google Scholar] [CrossRef]
- Mefteh, F.B.; Daoud, A.; Chenari Bouket, A.; Thissera, B.; Kadri, Y.; Cherif-Silini, H.; Eshelli, M.; Alenezi, F.N.; Vallat, A.; Oszako, T.; et al. Date palm trees root-derived endophytes as fungal cell factories for diverse bioactive metabolites. Int. J. Mol. Sci. 2018, 19, 1986. [Google Scholar] [CrossRef] [Green Version]
- Mefteh, F.B.; Daoud, A.; Chenari Bouket, A.; Alenezi, F.N.; Luptakova, L.; Rateb, M.E.; Kadri, A.; Gharsallah, N.; Belbahri, L. Fungal root microbiome from healthy and brittle leaf diseased date palm trees (Phoenix dactylifera L.) reveals a hidden untapped arsenal of antibacterial and broad spectrum antifungal secondary metabolites. Front. Microbiol. 2017, 8, 307. [Google Scholar] [CrossRef] [PubMed]
- Schouten, A. Endophytic fungi: Definitions, diversity, distribution and their significance in plant life. In Endophyte Biotechnology: Potential for Agriculture and Pharmacology; Schouten, A., Ed.; CABI Biotechnology Series: Wallingford, UK, 2019. [Google Scholar] [CrossRef]
- Liu, T.; Greenslade, A.; Yang, S. Levels of rhizome endophytic fungi fluctuate in Paris polyphylla var. yunnanensis as plants age. Plant Divers. 2017, 39, 60–64. [Google Scholar] [CrossRef]
- Ortega, H.E.; Torres-Mendoza, D.; Cubilla-Rios, L. Patents on endophytic fungi for agriculture and bio-and phytoremediation applications. Microorganisms 2020, 8, 1237. [Google Scholar] [CrossRef] [PubMed]
- Qader, M.M.; Hamed, A.A.; Soldatou, S.; Abdelraof, M.; Elawady, M.E.; Hassane, A.S.I.; Belbahri, L.; Ebel, R.; Rateb, M.E. Antimicrobial and antibiofilm activities of the fungal metabolites isolated from the marine endophytes Epicoccum nigrum M13 and Alternaria alternata 13A. Mar. Drugs 2021, 19, 232. [Google Scholar] [CrossRef] [PubMed]
- Pan, F.; Su, T.-J.; Cai, S.-M.; Wu, W. Fungal endophyte-derived Fritillaria unibracteata var. wabuensis: Diversity, antioxidant capacities in vitro and relations to phenolic, flavonoid or saponin compounds. Sci. Rep. 2017, 7, 42008. [Google Scholar]
- Emmanuel, O.C.; Babalola, O.O. Productivity and quality of horticultural crops through co-inoculation of arbuscular mycorrhizal fungi and plant growth promoting bacteria. Microbiol. Res. 2020, 239, 126569. [Google Scholar] [CrossRef] [PubMed]
- Igiehon, N.O.; Babalola, O.O.; Cheseto, X.; Torto, B. Effects of rhizobia and arbuscular mycorrhizal fungi on yield, size distribution and fatty acid of soybean seeds grown under drought stress. Microbiol. Res. 2021, 242, 126640. [Google Scholar] [CrossRef]
- Bérdy, J. Bioactive microbial metabolites. J. Antibiot. 2005, 58, 1–26. [Google Scholar] [CrossRef] [Green Version]
- Kusari, S.; Spiteller, M. Metabolomics of endophytic fungi producing associated plant secondary metabolites: Progress, challenges and opportunities. Metabolomics 2012, 10, 241–266. [Google Scholar]
- Hou, X.-M.; Wang, C.-Y.; Gerwick, W.H.; Shao, C.-L. Marine natural products as potential anti-tubercular agents. Eur. J. Med. Chem. 2019, 165, 273–292. [Google Scholar] [CrossRef]
- Skellam, E. Strategies for engineering natural product biosynthesis in fungi. Trends Biotechnol. 2019, 37, 416–427. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Stekel, D. First report of antimicrobial resistance pre-dates penicillin. Nature 2018, 562, 192. [Google Scholar] [CrossRef] [PubMed]
- Ibrar, M.; Ullah, M.W.; Manan, S.; Farooq, U.; Rafiq, M.; Hasan, F. Fungi from the extremes of life: An untapped treasure for bioactive compounds. Appl. Microbiol. Biotechnol. 2020, 104, 2777–2801. [Google Scholar] [CrossRef] [PubMed]
- Newman, D.J.; Cragg, G.M. Endophytic and epiphytic microbes as “sources” of bioactive agents. Front. Chem. 2015, 3, 34. [Google Scholar] [CrossRef]
- Zhu, L.; Chen, L. Progress in research on paclitaxel and tumor immunotherapy. Cell. Mol. Biol. Lett. 2019, 24, 40. [Google Scholar] [CrossRef] [Green Version]
- Kusari, S.; Singh, S.; Jayabaskaran, C. Rethinking production of Taxol® (paclitaxel) using endophyte biotechnology. Trends Biotechnol. 2014, 32, 304–311. [Google Scholar] [CrossRef]
- Kharwar, R.N.; Mishra, A.; Gond, S.K.; Stierle, A.; Stierle, D. Anticancer compounds derived from fungal endophytes: Their importance and future challenges. Nat. Prod. Rep. 2011, 28, 1208–1228. [Google Scholar] [CrossRef]
- Schueffler, A.; Anke, T. Fungal natural products in research and development. Nat. Prod. Rep. 2014, 31, 1425–1448. [Google Scholar] [CrossRef]
- Tawfike, A.F.; Romli, M.; Clements, C.; Abbott, G.; Young, L.; Schumacher, M.; Diederich, M.; Farage, M.; Edrada-Ebela, R. Isolation of anticancer and anti-trypanosome secondary metabolites from the endophytic fungus Aspergillus flocculus via bioactivity guided isolation and MS based metabolomics. J. Chromatogr. B 2019, 1106–1107, 71–83. [Google Scholar] [CrossRef] [Green Version]
- Fernandes, E.G.; Pereira, O.L.; da Silva, C.C.; Bento, C.B.P.; de Queiroz, M.V. Diversity of endophytic fungi in Glycine max. Microbiol. Res. 2015, 181, 84–92. [Google Scholar] [CrossRef] [PubMed]
- Shen, W.; Mao, H.; Huang, Q.; Dong, J. Benzenediol lactones: A class of fungal metabolites with diverse structural features and biological activities. Eur. J. Med. Chem. 2015, 97, 747–777. [Google Scholar] [CrossRef] [PubMed]
- Nielsen, J.C.; Nielsen, J. Development of fungal cell factories for the production of secondary metabolites: Linking genomics and metabolism. Synth. Syst. Biotechnol. 2017, 2, 5–12. [Google Scholar] [CrossRef]
- Martelli, G.; Giacomini, D. Antibacterial and antioxidant activities for natural and synthetic dual-active compounds. Eur. J. Med. Chem. 2018, 158, 91–105. [Google Scholar] [CrossRef] [PubMed]
- Adeleke, B.S.; Babalola, O.O. Pharmacological potential of fungal endophytes associated with medicinal plants: A review. J. Fungi. 2021, 7, 147. [Google Scholar] [CrossRef]
- El Sayed, A.S.A.; Sayed, M.T.; Rady, A.M.; Zein, N.; Enan, G.; Shindia, A.; El-Hefnawy, S.; Sitohy, M.; Sitohy, B. Exploiting the Biosynthetic Potency of Taxol from Fungal Endophytes of Conifers Plants; Genome Mining and Metabolic Manipulation. Molecules 2020, 25, 3000. [Google Scholar] [CrossRef]
- Guo, Z.; Zou, Z.-M. Discovery of New Secondary Metabolites by Epigenetic Regulation and NMR Comparison from the Plant Endophytic Fungus Monosporascus eutypoides. Molecules 2020, 25, 4192. [Google Scholar] [CrossRef] [PubMed]
- Kumar, G.; Chandra, P.; Choudhary, M. Endophytic fungi: A potential source of bioactive compounds. Chem. Sci. Rev. Lett. 2017, 6, 2373–2381. [Google Scholar]
- Akinola, S.A.; Babalola, O.O. The fungal and archaeal community within plant rhizosphere: A review on their contribution to crop safety. J. Plant Nutr. 2021, 44, 600–618. [Google Scholar] [CrossRef]
- Michel, J.; Abd Rani, N.Z.; Husain, K. A Review on the potential use of medicinal plants from Asteraceae and Lamiaceae plant family in cardiovascular diseases. Front. Pharmacol. 2020, 11, 852. [Google Scholar] [CrossRef] [PubMed]
- Savi, D.C.; Aluizio, R.; Glienke, C. Brazilian plants: An unexplored source of endophytes as producers of active metabolites. Planta Med. 2019, 85, 619–636. [Google Scholar]
- Bengtsson-Palme, J.; Kristiansson, E.; Larsson, D.J. Environmental factors influencing the development and spread of antibiotic resistance. FEMS Microbiol. Rev. 2018, 42, fux053. [Google Scholar] [CrossRef]
- Kraupner, N.; Ebmeyer, S.; Bengtsson-Palme, J.; Fick, J.; Kristiansson, E.; Flach, C.-F.; Larsson, D.G.J. Selective concentration for ciprofloxacin resistance in Escherichia coli grown in complex aquatic bacterial biofilms. Environ. Int. 2018, 116, 255–268. [Google Scholar] [CrossRef] [PubMed]
- Palanichamy, P.; Krishnamoorthy, G.; Kannan, S.; Marudhamuthu, M. Bioactive potential of secondary metabolites derived from medicinal plant endophytes. Egypt J. Basic Appl. Sci. 2018, 5, 303–312. [Google Scholar] [CrossRef] [Green Version]
- Manganyi, M.C.; Tchatchouang, C.-D.K.; Regnier, T.; Bezuidenhout, C.C.; Ateba, C.N. Bioactive compound produced by endophytic fungi isolated from Pelargonium sidoides against selected bacteria of clinical importance. Mycobiology 2019, 47, 335–339. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Tewari, D.; Rawat, P.; Singh, P.K. Adverse drug reactions of anticancer drugs derived from natural sources. Food Chem. Toxicol. 2019, 123, 522–535. [Google Scholar] [CrossRef]
- Chen, L.; Zhang, Q.-Y.; Jia, M.; Ming, Q.-L.; Yue, W.; Rahman, K.; Qin, L.-P.; Han, T. Endophytic fungi with antitumor activities: Their occurrence and anticancer compounds. Crit. Rev. Microbiol. 2016, 42, 454–473. [Google Scholar] [PubMed]
- Li, S.-J.; Zhang, X.; Wang, X.-H.; Zhao, C.-Q. Novel natural compounds from endophytic fungi with anticancer activity. Eur. J. Med. Chem. 2018, 156, 316–343. [Google Scholar] [CrossRef]
- Mishra, V.K.; Passari, A.K.; Chandra, P.; Leo, V.V.; Kumar, B.; Uthandi, S.; Thankappan, S.; Gupta, V.K.; Singh, B.P. Determination and production of antimicrobial compounds by Aspergillus clavatonanicus strain MJ31, an endophytic fungus from Mirabilis jalapa L. using UPLC-ESI-MS/MS and TD-GC-MS analysis. PLoS ONE 2017, 12, e0186234. [Google Scholar] [CrossRef] [Green Version]
- Raekiansyah, M.; Mori, M.; Nonaka, K.; Agoh, M.; Shiomi, K.; Matsumoto, A.; Morita, K. Identification of novel antiviral of fungus-derived brefeldin A against dengue viruses. Trop. Med. Health 2017, 45, 32. [Google Scholar] [CrossRef] [Green Version]
- Schön, T.; Miotto, P.; Köser, C.U.; Viveiros, M.; Böttger, E.; Cambau, E. Mycobacterium tuberculosis drug-resistance testing: Challenges, recent developments and perspectives. Clin. Microbiol. Infect. 2017, 23, 154–160. [Google Scholar] [CrossRef] [Green Version]
- Manganyi, M.C.; Regnier, T.; Kumar, A.; Bezuidenhout, C.C.; Ateba, C.N. Biodiversity and antibacterial screening of endophytic fungi isolated from Pelargonium sidoides. S. Afr. J. Bot. 2018, 116, 192–199. [Google Scholar] [CrossRef]
- Uzma, F.; Mohan, C.D.; Hashem, A.; Konappa, N.M.; Rangappa, S.; Kamath, P.V.; Singh, B.P.; Mudili, V.; Gupta, V.K.; Siddaiah, C.N.; et al. Endophytic fungi—Alternative sources of cytotoxic compounds: A review. Front. Pharmacol. 2018, 9, 309. [Google Scholar] [CrossRef]
- Kouipou Toghueo, R.M.; Boyom, F.F. Endophytic fungi from Terminalia species: A comprehensive review. J. Fungi 2019, 5, 43. [Google Scholar] [CrossRef]
- Nalin Rathnayake, G.R.; Savitri Kumar, N.; Jayasinghe, L.; Araya, H.; Fujimoto, Y. Secondary metabolites produced by an endophytic fungus Pestalotiopsis microspora. Nat. Prod. Bioprospect. 2019, 9, 411–417. [Google Scholar] [CrossRef] [Green Version]
- Ambele, C.F.; Ekesi, S.; Bisseleua, H.D.; Babalola, O.O.; Khamis, F.M.; Djuideu, C.T.; Akutse, K.S. Entomopathogenic fungi as endophytes for biological control of subterranean termite pests attacking cocoa seedlings. J. Fungi 2020, 6, 126. [Google Scholar] [CrossRef]
- Bacon, C.W.; White, J.F. Functions, mechanisms and regulation of endophytic and epiphytic microbial communities of plants. Symbiosis 2016, 68, 87–98. [Google Scholar] [CrossRef]
- Yan, L.; Zhu, J.; Zhao, X.; Shi, J.; Jiang, C.; Shao, D. Beneficial effects of endophytic fungi colonization on plants. Appl. Microbiol. Biotechnol. 2019, 103, 3327–3340. [Google Scholar] [CrossRef] [PubMed]
- Khiralla, A.; Spina, R.; Yagi, S.; Mohamed, I.; Laurain-Mattar, D. Endophytic fungi: Occurrence, classification, function and natural products. In Endophytic Fungi: Diversity, Characterization and Biocontrol; Nova Publishers: New York, NY, USA, 2016; pp. 1–19. [Google Scholar]
- Latz, M.A.; Jensen, B.; Collinge, D.B.; Jørgensen, H.J. Endophytic fungi as biocontrol agents: Elucidating mechanisms in disease suppression. Plant Ecol. Divers. 2018, 11, 555–567. [Google Scholar] [CrossRef] [Green Version]
- Bamisile, B.S.; Dash, C.K.; Akutse, K.S.; Keppanan, R.; Afolabi, O.G.; Hussain, M.; Qasim, M.; Wang, L. Prospects of endophytic fungal entomopathogens as biocontrol and plant growth promoting agents: An insight on how artificial inoculation methods affect endophytic colonization of host plants. Microbiol. Res. 2018, 217, 34–50. [Google Scholar] [CrossRef] [PubMed]
- Cheffi, M.; Chenari Bouket, A.; Alenezi, F.N.; Luptakova, L.; Belka, M.; Vallat, A.; Rateb, M.E.; Tounsi, S.; Triki, M.A.; Belbahri, L. Olea europaea L. root endophyte Bacillus velezensis OEE1 counteracts oomycete and fungal harmful pathogens and harbours a large repertoire of secreted and volatile metabolites and beneficial functional genes. Microorganisms 2019, 7, 314. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Bilal, S.; Shahzad, R.; Imran, M.; Jan, R.; Kim, K.M.; Lee, I.-J. Synergistic association of endophytic fungi enhances Glycine max L. resilience to combined abiotic stresses: Heavy metals, high temperature and drought stress. Ind. Crops Prod. 2020, 143, 111931. [Google Scholar] [CrossRef]
- Suryanarayanan, T.S.; Thirunavukkarasu, N.; Govindarajulu, M.B.; Gopalan, V. Fungal endophytes: An untapped source of biocatalysts. Fungal Divers. 2012, 54, 19–30. [Google Scholar] [CrossRef]
- Mefteh, F.B.; Frikha, F.; Daoud, A.; Chenari Bouket, A.; Luptakova, L.; Alenezi, F.N.; Al-Anzi, B.S.; Oszako, T.; Gharsallah, N.; Belbahri, L. Response surface methodology optimization of an acidic protease produced by Penicillium bilaiae isolate TDPEF30, a newly recovered endophytic fungus from healthy roots of date palm trees (Phoenix dactylifera L.). Microorganisms 2019, 7, 74. [Google Scholar] [CrossRef] [Green Version]
- Jagannath, S.; Konappa, N.; Lokesh, A.; Dasegowda, T.; Udayashankar, A.C.; Chowdappa, S.; Cheluviah, M.; Satapute, P.; Jogaiah, S. Bioactive compounds guided diversity of endophytic fungi from Baliospermum montanum and their potential extracellular enzymes. Anal. Biochem. 2021, 614, 114024. [Google Scholar] [CrossRef]
- Traving, S.J.; Thygesen, U.H.; Riemann, L.; Stedmon, C.A. A model of extracellular enzymes in free-living microbes: Which strategy pays off? Appl. Environ. Microbiol. 2015, 81, 7385. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Yadav, A.N.; Kumar, R.; Kumar, S.; Kumar, V.; Sugitha, T.; Singh, B.; Chauahan, V.S.; Dhaliwal, H.S.; Saxena, A.K. Beneficial microbiomes: Biodiversity and potential biotechnological applications for sustainable agriculture and human health. J. Appl. Biol. Biotechnol. 2017, 5, 45–57. [Google Scholar]
- Shubha, J.; Srinivas, C. Diversity and extracellular enzymes of endophytic fungi associated with Cymbidium aloifolium L. Afr. J. Biotechnol. 2017, 16, 2248–2258. [Google Scholar]
- Srilakshmi, J.; Madhavi, J.; Lavanya, S.; Ammani, K. Commercial Potential of Fungal Protease: Past, Present and Future Prospects. J. Pharmaceut. Chem. Biol. Sci. 2015, 2, 218–234. [Google Scholar]
- Sahay, H.; Yadav, A.N.; Singh, A.K.; Singh, S.; Kaushik, R.; Saxena, A.K. Hot springs of Indian Himalayas: Potential sources of microbial diversity and thermostable hydrolytic enzymes. 3 Biotech 2017, 7, 118. [Google Scholar] [CrossRef] [Green Version]
- Rajput, K.; Chanyal, S.; Agrawal, P.K. Optimization of protease production by endophytic fungus, Alternaria alternata isolated from gymnosperm tree Cupressus torulosa D Don. World J. Pharm. Pharmaceut. Sci. 2016, 5, 1034–1054. [Google Scholar]
- dos Santos Aguilar, J.G.; Sato, H.H. Microbial proteases: Production and application in obtaining protein hydrolysates. Food Res. Int. 2018, 103, 253–262. [Google Scholar] [CrossRef] [PubMed]
- Yadav, R.; Singh, A.V.; Joshi, S.; Kumar, M. Antifungal and enzyme activity of endophytic fungi isolated from Ocimum sanctum and Aloe vera. Afr. J. Microbiol. Res. 2015, 9, 1783–1788. [Google Scholar]
- Archna, S.; Priyank, V.; Nath, Y.A.; Kumar, S.A. Bioprospecting for extracellular hydrolytic enzymes from culturable thermotolerant bacteria isolated from Manikaran thermal springs. Res. J. Biotechnol. 2015, 10, 4. [Google Scholar]
- Thomas, L.; Joseph, A.; Singhania, R.R.; Patel, A.K.; Pandey, A. Industrial enzymes: Xylanases. In Current Developments in Biotechnology and Bioengineering; Pandey, A., Negi, S., Soccol, C.R., Eds.; Elsevier: Amsterdam, The Netherlands, 2017; pp. 127–148. [Google Scholar]
- Singh, R.V.; Sambyal, K.; Negi, A.; Sonwani, S.; Mahajan, R. Chitinases production: A robust enzyme and its industrial applications. Biocatal. Biotransfor. 2021, 39, 161–189. [Google Scholar] [CrossRef]
- Liaqat, F.; Eltem, R. Chitooligosaccharides and their biological activities: A comprehensive review. Carbohydr. Polym. 2018, 184, 243–259. [Google Scholar] [CrossRef]
- Le, B.; Yang, S.H. Microbial chitinases: Properties, current state and biotechnological applications. World J. Microbiol. Biotechnol. 2019, 35, 144. [Google Scholar] [CrossRef]
- Hartl, L.; Zach, S.; Seidl-Seiboth, V. Fungal chitinases: Diversity, mechanistic properties and biotechnological potential. Appl. Microbiol. Biotechnol. 2012, 93, 533–543. [Google Scholar] [CrossRef] [Green Version]
- Gomaa, E.Z. Microbial chitinases: Properties, enhancement and potential applications. Protoplasma 2021, 258, 695–710. [Google Scholar] [CrossRef]
- Mathew, G.M.; Madhavan, A.; Arun, K.B.; Sindhu, R.; Binod, P.; Singhania, R.R.; Sukumaran, R.K.; Pandey, A. Thermophilic chitinases: Structural, functional and engineering attributes for industrial applications. Appl. Biochem. Biotechnol. 2021, 193, 142–164. [Google Scholar] [CrossRef] [PubMed]
- Makky, E.A.; Yusoff, M.M. Bioeconomy: Pectinases purification and application of fermented waste from Thermomyces lanuginosus. J. Med. Bioeng. 2015, 4, 76–80. [Google Scholar] [CrossRef]
- Garg, G.; Singh, A.; Kaur, A.; Singh, R.; Kaur, J.; Mahajan, R. Microbial pectinases: An ecofriendly tool of nature for industries. 3 Biotech 2016, 6, 47. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Pušić, T.; Tarbuk, A.; Dekanić, T. Bio-innovation in cotton fabric scouring-acid and neutral pectinases. Fibres Text. East. Eur. 2015, 109, 98–103. [Google Scholar]
- Ghanbarzadeh, B.; Ataeefard, M.; Etezad, S.M.; Mahdavi, S. Enzymatic deinking of office waste printed paper: Optimization via response surface methodology. Biomass. Conv. Bioref. 2021. [Google Scholar] [CrossRef]
- Singh, A.; Kaur, A.; Dua, A.; Mahajan, R. An efficient and improved methodology for the screening of industrially valuable xylano-pectino-cellulolytic microbes. Enzyme Res. 2015, 2015, 725281. [Google Scholar] [CrossRef] [PubMed]
- Oliveira, A.C.D.; Watanabe, F.M.F.; Vargas, J.V.C.; Rodrigues, M.L.F.; Mariano, A.B. Production of methyl oleate with a lipase from an endophytic yeast isolated from castor leaves. Biocatal. Agric. Biotechnol. 2012, 1, 295–300. [Google Scholar] [CrossRef]
- Gopinath, S.C.; Anbu, P.; Lakshmipriya, T.; Hilda, A. Strategies to characterize fungal lipases for applications in medicine and dairy industry. BioMed Res. Int. 2013, 2013, 154549. [Google Scholar] [CrossRef]
- Kaur, R.; Saxena, A.; Sangwan, P.; Yadav, A.N.; Kumar, V.; Dhaliwal, H.S. Production and characterization of a neutral phytase of Penicillium oxalicum EUFR-3 isolated from Himalayan region. Nusantara Biosci. 2017, 9, 68–76. [Google Scholar] [CrossRef]
- Yadav, A.N.; Kumar, V.; Dhaliwal, H.S.; Prasad, R.; Saxena, A.K. Microbiome in crops: Diversity, distribution, and potential role in crop improvement. In Crop Improvement through Microbial Biotechnology; Prasad, R., Gill, S.S., Tuteja, N., Eds.; Elsevier: Noita, India, 2018; pp. 305–332. [Google Scholar]
- Toghueo, R.M.K.; Zabalgogeazcoa, I.; de Aldana, B.V.; Boyom, F.F. Enzymatic activity of endophytic fungi from the medicinal plants Terminalia catappa, Terminalia mantaly and Cananga odorata. S. Afr. J. Bot. 2017, 109, 146–153. [Google Scholar] [CrossRef]
- Nandy, S.; Das, T.; Tudu, C.K.; Pandey, D.K.; Dey, A.; Ray, P. Fungal endophytes: Futuristic tool in recent research area of phytoremediation. S. Afr. J. Bot. 2020, 134, 285–295. [Google Scholar] [CrossRef]
- Pietro-Souza, W.; de Campos Pereira, F.; Mello, I.S.; Stachack, F.F.F.; Terezo, A.J.; da Cunha, C.N.; White, J.F.; Li, H.; Soares, M.A. Mercury resistance and bioremediation mediated by endophytic fungi. Chemosphere 2020, 240, 124874. [Google Scholar] [CrossRef]
- Zahoor, M.; Irshad, M.; Rahman, H.; Qasim, M.; Afridi, S.G.; Qadir, M.; Hussain, A. Alleviation of heavy metal toxicity and phytostimulation of Brassica campestris L. by endophytic Mucor sp. MHR-7. Ecotoxicol. Environ. Saf. 2017, 142, 139–149. [Google Scholar] [CrossRef]
- Ripa, F.A.; Cao, W.; Tong, S.; Sun, J. Assessment of plant growth promoting and abiotic stress tolerance properties of wheat endophytic fungi. BioMed Res. Int. 2019. [Google Scholar] [CrossRef]
- Bier, M.C.J.; Medeiros, A.B.P.; Soccol, C.R. Biotransformation of limonene by an endophytic fungus using synthetic and orange residue-based media. Fungal Biol. 2017, 121, 137–144. [Google Scholar] [CrossRef] [PubMed]
- Krishnamurthy, Y.L.; Naik, B.S. Endophytic Fungi Bioremediation. In Endophytes: Crop Productivity and Protection: Volume 2 Sustainable Development and Biodiversity; Maheshwari, D.K., Annapurna, K., Eds.; Springer: Cham, Switzerland, 2017; pp. 47–60. [Google Scholar] [CrossRef]
- He, W.; Megharaj, M.; Wu, C.-Y.; Subashchandrabose, S.R.; Dai, C.-C. Endophyte-assisted phytoremediation: Mechanisms and current application strategies for soil mixed pollutants. Crit. Rev. Biotechnol. 2020, 40, 31–45. [Google Scholar] [CrossRef]
- Deng, Z.; Cao, L. Fungal endophytes and their interactions with plants in phytoremediation: A review. Chemosphere 2017, 168, 1100–1106. [Google Scholar] [CrossRef]
- Moffat, J.G.; Vincent, F.; Lee, J.A.; Eder, J.; Prunotto, M. Opportunities and challenges in phenotypic drug discovery: An industry perspective. Nat. Rev. Drug Discov. 2017, 16, 531–543. [Google Scholar] [CrossRef]
- Atanasov, A.G.; Zotchev, S.B.; Dirsch, V.M.; Supuran, C.T. Natural products in drug discovery: Advances and opportunities. Nat. Rev. Drug Discov. 2021, 20, 200–216. [Google Scholar] [CrossRef] [PubMed]
- van der Lee, T.A.; Medema, M.H. Computational strategies for genome-based natural product discovery and engineering in fungi. Fungal Genet. Biol. 2016, 89, 29–36. [Google Scholar] [CrossRef] [Green Version]
- Schirle, M.; Jenkins, J.L. Identifying compound efficacy targets in phenotypic drug discovery. Drug Discov. Today 2016, 21, 82–89. [Google Scholar] [CrossRef] [PubMed]
- Sagita, R.; Quax, W.J.; Haslinger, K. Current state and future directions of genetics and genomics of endophytic fungi for bioprospecting efforts. Front. Bioeng. Biotechnol. 2021, 9, 170. [Google Scholar] [CrossRef] [PubMed]
- Belbahri, L.; Chenari Bouket, A.; Rekik, I.; Alenezi, F.N.; Vallat, A.; Luptakova, L.; Petrovova, E.; Oszako, T.; Cherrad, S.; Vacher, S.; et al. Comparative genomics of Bacillus amyloliquefaciens strains reveals a core genome with traits for habitat adaptation and a secondary metabolites rich accessory genome. Front. Microbiol. 2017, 8, 1438. [Google Scholar] [CrossRef] [PubMed]
- Reynolds, H.T.; Slot, J.C.; Divon, H.H.; Lysøe, E.; Proctor, R.H.; Brown, D.W. Differential retention of gene functions in a secondary metabolite cluster. Mol. Biol. Evol. 2017, 34, 2002–2015. [Google Scholar] [CrossRef] [PubMed]
- Chavali, A.K.; Rhee, S.Y. Bioinformatics tools for the identification of gene clusters that biosynthesize specialized metabolites. Brief. Bioinf. 2018, 19, 1022–1034. [Google Scholar] [CrossRef]
- Loureiro, C.; Medema, M.H.; van der Oost, J.; Sipkema, D. Exploration and exploitation of the environment for novel specialized metabolites. Curr. Opin. Biotechnol. 2018, 50, 206–213. [Google Scholar] [CrossRef] [Green Version]
- Chiang, Y.-M.; Ahuja, M.; Oakley, C.E.; Entwistle, R.; Asokan, A.; Zutz, C.; Wang, C.C.C.; Oakley, B.R. Development of genetic dereplication strains in Aspergillus nidulans results in the discovery of aspercryptin. Angew. Chem. 2016, 128, 1694–1697. [Google Scholar] [CrossRef] [Green Version]
- Mohimani, H.; Gurevich, A.; Shlemov, A.; Mikheenko, A.; Korobeynikov, A.; Cao, L.; Shcherbin, E.; Nothias, L.-F.; Dorrestein, P.C.; Pevzner, P.A. Dereplication of microbial metabolites through database search of mass spectra. Nat. Commun. 2018, 9, 4035. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Zhang, X.; Li, S.-J.; Li, J.-J.; Liang, Z.-Z.; Zhao, C.-Q. Novel natural products from extremophilic fungi. Mar. Drugs 2018, 16, 194. [Google Scholar] [CrossRef] [Green Version]
- El-Moslamy, S.H.; Elkady, M.F.; Rezk, A.H.; Abdel-Fattah, Y.R. Applying taguchi design and large-scale strategy for mycosynthesis of nano-silver from endophytic Trichoderma harzianum SYA. F4 and its application against phytopathogens. Sci. Rep. 2017, 7, 45297. [Google Scholar] [CrossRef] [Green Version]
- Wang, Y.; Li, H.; Feng, G.; Du, L.; Zeng, D. Biodegradation of diuron by an endophytic fungus Neurospora intermedia DP8-1 isolated from sugarcane and its potential for remediating diuron-contaminated soils. PLoS ONE 2017, 12, e0182556. [Google Scholar] [CrossRef] [Green Version]
- Sekurova, O.N.; Schneider, O.; Zotchev, S.B. Novel bioactive natural products from bacteria via bioprospecting, genome mining and metabolic engineering. Microb. Biotechnol. 2019, 12, 828–844. [Google Scholar] [CrossRef] [Green Version]
- Bertrand, S.; Bohni, N.; Schnee, S.; Schumpp, O.; Gindro, K.; Wolfender, J.-L. Metabolite induction via microorganism co-culture: A potential way to enhance chemical diversity for drug discovery. Biotechnol. Adv. 2014, 32, 1180–1204. [Google Scholar] [CrossRef]
- Adnani, N.; Rajski, S.R.; Bugni, T.S. Symbiosis-inspired approaches to antibiotic discovery. Nat. Prod. Rep. 2017, 34, 784–814. [Google Scholar] [CrossRef]
- Wu, B.; Hussain, M.; Zhang, W.; Stadler, M.; Liu, X.; Xiang, M. Current insights into fungal species diversity and perspective on naming the environmental DNA sequences of fungi. Mycology 2019, 10, 127–140. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Ochi, K. From microbial differentiation to ribosome engineering. Biosci. Biotechnol. Biochem. 2007, 71, 1373–1386. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Ochi, K.; Tanaka, Y.; Tojo, S. Activating the expression of bacterial cryptic genes by rpoB mutations in RNA polymerase or by rare earth elements. J. Ind. Microbiol. Biotechnol. 2014, 41, 403–414. [Google Scholar] [CrossRef]
- Williams, R.B.; Henrikson, J.C.; Hoover, A.R.; Lee, A.E.; Cichewicz, R.H. Epigenetic remodeling of the fungal secondary metabolome. Org. Biomol. Chem. 2008, 6, 1895–1897. [Google Scholar] [CrossRef]
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
Slama, H.B.; Chenari Bouket, A.; Alenezi, F.N.; Pourhassan, Z.; Golińska, P.; Oszako, T.; Belbahri, L. Potentials of Endophytic Fungi in the Biosynthesis of Versatile Secondary Metabolites and Enzymes. Forests 2021, 12, 1784. https://doi.org/10.3390/f12121784
Slama HB, Chenari Bouket A, Alenezi FN, Pourhassan Z, Golińska P, Oszako T, Belbahri L. Potentials of Endophytic Fungi in the Biosynthesis of Versatile Secondary Metabolites and Enzymes. Forests. 2021; 12(12):1784. https://doi.org/10.3390/f12121784
Chicago/Turabian StyleSlama, Houda Ben, Ali Chenari Bouket, Faizah N. Alenezi, Zeinab Pourhassan, Patrycja Golińska, Tomasz Oszako, and Lassaad Belbahri. 2021. "Potentials of Endophytic Fungi in the Biosynthesis of Versatile Secondary Metabolites and Enzymes" Forests 12, no. 12: 1784. https://doi.org/10.3390/f12121784
APA StyleSlama, H. B., Chenari Bouket, A., Alenezi, F. N., Pourhassan, Z., Golińska, P., Oszako, T., & Belbahri, L. (2021). Potentials of Endophytic Fungi in the Biosynthesis of Versatile Secondary Metabolites and Enzymes. Forests, 12(12), 1784. https://doi.org/10.3390/f12121784