Taxonomic Positions and Secondary Metabolite-Biosynthetic Gene Clusters of Akazaoxime- and Levantilide-Producers
1
Biological Resource Center, National Institute of Technology and Evaluation (NBRC), Chiba 292-0818, Japan
2
Biotechnology Research Center and Department of Biotechnology, Toyama Prefectural University, Toyama 939-0398, Japan
*
Author to whom correspondence should be addressed.
Life 2023, 13(2), 542; https://doi.org/10.3390/life13020542
Submission received: 15 December 2022
/
Revised: 8 February 2023
/
Accepted: 10 February 2023
/
Published: 15 February 2023
(This article belongs to the Special Issue New Insights into Marine Drugs Discovery)
Abstract
:Micromonospora sp. AKA109 is a producer of akazaoxime and A-76356, whereas Micromonospora sp. AKA38 is that of levantilide C. We aimed to clarify their taxonomic positions and identify biosynthetic gene clusters (BGCs) of these compounds. In 16S rRNA gene and DNA gyrase subunit B gene (gyrB) sequence analyses, strains AKA109 and AKA38 were the most closely related to Micromonospora humidisoli MMS20-R2-29T and Micromonospora schwarzwaldensis HKI0641T, respectively. Although Micromonospora sp. AKA109 was identified as M. humidisoli by the gyrB sequence similarity and DNA–DNA relatedness based on whole genome sequences, Micromonospora sp. AKA38 was classified to a new genomospecies. M. humidisoli AKA109 harbored six type-I polyketide synthase (PKS), one type-II PKS, one type-III PKS, three non-ribosomal peptide synthetase (NRPS) and three hybrid PKS/NRPS gene clusters, among which the BGC of akazaoxime and A-76356 was identified. These gene clusters are conserved in M. humidisoli MMS20-R2-29T. Micromonospora sp. AKA38 harbored two type-I PKS, one of which was responsible for levantilide C, one type-II PKS, one type-III PKS, two NRPS and five hybrid PKS/NRPS gene clusters. We predicted products derived from these gene clusters through bioinformatic analyses. Consequently, these two strains are revealed to be promising sources for diverse non-ribosomal peptide and polyketide compounds.
1. Introduction
Actinomycetes are Gram stain-positive and filamentous bacteria with high G + C contents in genomic DNAs. They are well known as a promising source for pharmacologically useful bioactive substances with diverse chemistries, from which many pharmaceuticals were developed and are clinically used [1]. The genus Streptomyces is the representative of actinomycetes, and its main habitat is soil. However, soil environments are extensively searched for novel actinomycetes, and consequently, it is getting harder to isolate novel actinomycetal strains from the same environments. In contrast, marine environments are attracting attention as rich sources of underexplored actinomycetes. Indeed, we have discovered new and diverse bioactive secondary metabolites from marine actinomycetes [2,3,4,5,6,7,8,9]. Micromonospora strains are frequently isolated from marine environments. Many bioactive substances are reported from this genus [10,11]. We previously isolated Micromonospora sp. AKA109 and Micromonospora sp. AKA38 from deep sea water. From Micromonospora sp. AKA109, a new compound named akazaoxime (1, Figure 1) was discovered, along with a known compound, A-76356 (2, Figure 1). Akazaoxime and A-76356 are enteromycin-class antibiotics. Incorporation experiments of labelled precursors suggested these two compounds are biosynthesized from glycine, leucin and propionate. Akazaoxime exhibits antibacterial activity to Gram-positive Kocuria rhizophila, whereas A-76356 is active against filamentous fungi such as the plant pathogen Glomerella cingulata [12]. Micromonospora sp. AKA38 produces levantilide C (3, Figure 1), which is a 20-membered macrolide and exhibits antiproliferative activities against several tumor cell lines [13]. Biosynthetic gene clusters (BGCs) of these compounds have not been identified yet, although identification of BGCs plays an important role in developments in combinatorial biosynthesis and synthetic biology.
Polyketides such as macrolide backbones are biosynthesized by the assemblage of acyl-CoAs as building blocks. The assembly is catalyzed by polyketide synthases (PKSs). PKSs are classified by three types. Type-I PKSs are large modular enzymes composed of multiple catalytic domains. Polyketide chains are synthesized according to the co-linearity rule of assembly lines. Such a mechanism shows similarity to that in the biosynthesis of non-ribosomal peptides by non-ribosomal peptide synthetases (NRPSs), which is based on assembly of amino acids as building blocks. NRPSs as well as type-I PKSs are large and modular enzymes with multiple catalytic domains, and they accord to the co-linearity rule [14,15]. Polyketide chains for macrolide compounds are synthesized by type-I PKSs. Backbones synthesized by type-I PKSs and/or NRPSs can be predicted from their domain organizations by bioinformatic analysis [14,15]. In contrast, type-II PKSs are composed of three monofunctional enzymes, ketosynthase α (KSα), KSβ (chain length factor), and acyl carrier protein (ACP). Differently from type-I PKSs, these three enzymes iteratively catalyze multiple chain elongation steps. The main products of type-II PKSs are aromatic compounds [16]. Type-III PKSs are not multimodular or composed of abovementioned three enzymes, but stand alone with a KS domain and iteratively catalyze the assembly of the acyl-CoA unit [17]. Genome analyses revealed that half to three quarters of the secondary metabolite-BGCs in each actinomycetal genome are associated with PKSs or NRPSs. This suggests that polyketides, non-ribosomal peptides, and their hybrid compounds, which are derived from hybrid PKS/NRPS gene clusters, are main secondary metabolites in actinomycetes [18].
In the present study, we classified Micromonospora sp. AKA109 and Micromonospora sp. AKA38 at species level. Next, we identified BGCs for akazaoxime/A-76356 and levantilide C through analysis of PKS and NRPS gene clusters in their genomes. The analysis revealed the potential of the two strains to act as producers of diverse polyketide- and nonribosomal peptide-compounds. These results are useful to elucidate potential products of each strain.
2. Materials and Methods
Micromonospora strains AKA109 and AKA38 were isolated from deep sea water collected in Shizuoka, Japan, maintained as TP-A0907 and TP-A0908, respectively, in Toyama Prefectural University, and have been deposited to and are available from the NBRC culture collection as NBRC 113680 and NBRC 113681, respectively. The 16S rRNA genes were amplified by PCR using 9F and 1541R primers. The amplicons were sequenced by the method described in our previous report [19]. Type strains showing high 16S rRNA gene sequence similarities to AKA109 and AKA38 were searched using the EzBioCloud web server [20]. Phylogenetic trees based on 16S rRNA gene and DNA gyrase subunit B gene (gyrB) sequences were reconstructed by the neighbor-joining method using ClustalX 2.1. Whole genomes were sequenced using PacBio, as reported [21]. Draft genome sequences of strains AKA109 and AKA38 were deposited to DDBJ under the accession numbers of BNEH01000001–BNEH01000007 and BNEI01000001–BNEI01000011, respectively. A phylogenomic tree was reconstructed using the TYSG server [22]. DNA–DNA relatedness was calculated by digital DNA–DNA hybridization (DDH) using the Genome-to-Genome Distance Calculator 2.1 (GGDC) [23], and DDH estimates by the Formula 2 were employed. PKS and NRPS gene clusters in the whole genome were searched, and their domains were determined using antiSMASH [24]. The products were predicted by reviewing module numbers and domain organizations in PKSs and NRPSs, the substrates of acyltransferase (AT) and adenylation (A) domains, and orthologs searched by BLAST, in addition to results of ClusterBlast in antiSMASH.
3. Results
3.1. Classification of Micromonospora Strains AKA109 and AKA38
In the 16S rRNA gene sequence analysis, Micromonospora sp. AKA109 showed 100% similarity to Micromonospora humidisoli MMS20-R2-29T, whereas Micromonospora sp. AKA38 showed 99.9% similarity to Micromonospora schwarzwaldensis HKI0641T as the closest. In the phylogenetic tree shown in Figure 2, strain AKA109 formed an independent clade with M. humidisoli MMS20-R2-29T, whereas strain AKA38 did that with M. schwarzwaldensis HKI0641T.
We next reconstructed a phylogenetic tree based on gyrB sequences, as shown in Figure 3, since gyrB sequences are recognized to be more suitable than 16S rRNA gene sequences for phylogenetic classification and identification [25]. In this tree, M. humidisoli and M. schwarzwaldensis were also phylogenetically the closest species of strains AKA109 and AKA38, respectively. The gyrB sequence similarity between Micromonospora sp. AKA109 and M. humidisoli MMS20-R2-29T was 99.0%. Since 98.5% in gyrB sequence similarity is recognized to correspond to 70% in DNA–DNA relatedness [25,26], Micromonospora sp. AKA109 is likely M. humidisoli. In contrast, the gyrB sequence similarity between Micromonospora sp. AKA38 and M. schwarzwaldensis HKI0641T was 97.4%, which is much below than 98.5%; therefore, Micromonospora sp. AKA38 is considered an independent new genomospecies.
Additionally, a phylogenomic tree was reconstructed with type strains whose whole genome sequences are published (Figure 4). The phylogenetic relationships well correlated to those in phylogenetic trees of Figure 1 and Figure 2. DNA–DNA relatedness, estimated by digital DDH, between Micromonospora sp. AKA109 and M. humidisoli MMS20-R2-29T was 93.5%. As this value is much higher than 70%, which is the established cut-off for species delineation [27,28,29], strain AKA109 was identified to be M. humidisoli. In contrast, DNA–DNA relatedness between Micromonospora sp. AKA38 and the other strains shown in Figure 4 were less than 41.4%. This result also shows Micromonospora sp. AKA38 to be an independent genomospecies.
3.2. PKS and NRPS Gene Clusters in the Whole Genome of M. humidisoli AKA109
Six type-I PKS, one type-II PKS, one type-III PKS, three NRPS and three hybrid PKS/NRPS gene clusters were encoded in the genome of Micromonospora sp. AKA109. Type-I PKS gene cluster 1 (t1pks-1) encoded three PKSs, whose domain organization was almost identical to those (KS ATm ACP KS ATm DH KR ACP KS ATm DH KR ACP, KS ATm DH KR ACP KS ATm DH KR ACP, KS ATm/mm/em DH KR ACP TD) of camporidine-, argimycin- and streptazone-BGCs [30,31,32]. However, t1pks-1 lacked the KR domain (underlined in the previous brackets) present in CamD, ArpII and StzC. Although the substrate of the last AT domain in t1pks-1 was methylmalonyl-CoA, those in ArpIII and StzB are malonyl-CoA. Thus, product(s) of t1pks-1 may resemble camporidine, argimycin or streptazone, but will be different from these. PKSs encoded in t1pks-2, t1pks-3 and t1pks-4 did not show high sequence similarities to PKSs whose products have been identified. Thus, the products of these PKS gene clusters were not predicted. The domain organization, KS/AT/KR/DH, of the PKS encoded by TPA0907_18690 in t1pks-3 is well known as that of iterative PKSs for enediyne syntheses. Hence, the products of t1pks-3 may include an enediyne moiety. T1pks-5 encoded five PKSs. These PKSs showed high similarities to those in the marinolactam-BGC (mrl) [33]. Their domain organization was identical to that of mrl except for the presence of a DH domain in the first module of MrlB, which is absent in that of TPA0907_35890. Therefore, we annotated this cluster to be responsible for a marinolactum congener. As genes in t1pks-6 showed high similarities to those in the amycomicin-BGC, the product was predicted to be amycomicin. Products of type-II PKS gene cluster 1 (t2pks-1) were predicted to be an aromatic compound. Type-III PKS gene cluster 1 (t3pks-1) showed similarity to agq, which is the BGC of alkyl-O-dihydrogeranyl-methoxyhydroquinone [34]. Three NRPS gene clusters (nrps-1, nrps-2, and nrps-3) did not show high similarities to those whose products are elucidated, suggesting that they are orphan gene clusters. Although the product of nrps-2 was unpredictable because its NRPS was not multimodular, those of nrps-1 and nrps-3 were predicted as dipeptide and tetrapeptide, respectively, as shown in Table 1. Hybrid PKS/NRPS gene clusters 1 and 2 (pks/nrps-1 and pks/nrps-2) were orphan. The domain organization of pks/nrps-1 was unusual, because thioesterase (TE) domain is not present at the terminal, but as the first domain. Hence, it is doubtful that the cluster works to synthesize hybrid polyketide/non-ribosomal peptide compounds. The product derived from pks/nrps-2 was predicted to be a hybrid polyketide/non-ribosomal peptide compound including Asn and Ser residues.
We considered pks/nrps-3 to be the BGC for akazaoxime and A-76356, according to its domain organization and the biosynthetic pathway revealed by incorporation of labeled precursors [12]. These two compounds have been reported to be synthesized from glycine, leucine, and propionate. Similarly, pks/nrps-3 encodes two NRPS and one PKS, which incorporate two amino acids and one acyl-CoA, respectively, to the product. One of the amino acids was predicted to be leucine, although the other was bioinformatically not. Presence of a KR domain in the PKS well accounts for hydration of the keto group derived from carboxyl group of leucine. The cluster encoded a diiron oxygenase and a nitronate O-methyltransferase, which are essential to form aldoxime functionality and an O-methyl nitronic acid moiety [35]. We predicted the biosynthetic pathway of akazaoxime and A-76356, as shown Figure 5. A glycine molecule is loaded on the NRPS encoded by TPA0907_56660. Its amino group is converted to an aldoxime functionality through an intermediate by the diiron oxygenase, as reported in the biosynthesis of althiomycin [35,36]. If the methyltransferase encoded by TPA0907_56720 acts the intermediate, the amino group is converted to O-methyl nitronic acid moiety, as reported in the biosynthesis of enteromycin carboxamide [35]. To the modified glycine molecules, leucine and methylmalonyl-CoA are bound by the other NRPS (TPA0907_56840) and the PKS (TPA0907_56670). Finally, the chains are released from the PKS to yield akazaoxime (1) and A-76356 (2), respectively.
3.3. PKS and NRPS Gene Clusters in the Whole Genome of Micromonospora sp. AKA38
Micromonospora sp. AKA38 harbored two type-I PKS, one type-II PKS, one type-III PKS, two NRPS and five hybrid PKS/NRPS gene clusters in its genome, as listed in Table 2.
We annotated t1pks-7 as the BGC of levantilide C, according to its domain organization and the chemical structure. The cluster encoded three PKSs including a loading module and eleven modules to incorporate acyl-CoAs in the polyketide chain, as shown in Figure 6. The chemical structure predicted by the domain organization well matched to that of levantilide C. DH and ER domains in module 3 and the DH domain in module 8 would be inactive considering the actual chemical structure of levantilide C. A hydroxyl group is present at C-10 in levantilide C, and it does not form by polyketide biosynthesis. Because a cytochrome P450 is encoded near the PKSs in the gene cluster as TPA0908_40790, the hydroxyl group is likely introduced by the cytochrome P450.
T1pks-8 is a large type-I PKS gene cluster encoding 13 PKSs, which form 33 modules. The product was predicted to be quinolidomicin based on the domain organization and similarities to quinolidomicin’s PKSs (QmnA1 to QmnA13) [37]. The gene cluster is widely distributed in the genus Micromonospora [38]. The product of t2pks-2 could not be predicted because the type-II PKSs did not show high sequence similarities to enzymes for the reported compounds. In most type-II PKS gene clusters, an ACP is encoded downstream of KSβ (CLF), but the ACP of t2pks-2 is upstream of KSα and includes a cyclase domain. Two gene clusters, t3pks-1 and pks/nrps-2, asterisked in the tables, were orthologs of those present in M. humidisoli AKA109. The other gene clusters, such as nrps-4, nrps-5, pks/nrps-4, pks/nrps-5, pks/nrps-6 and pks/nrps-7, were orphan, and their products were predicted as shown in Table 2. In pks/nrps-7, two type-I PKSs whose domain organizations are KS-AT-KR-DH and KS-AT-ACP, respectively and one type-III PKS were encoded in addition to NRPSs. The domain pair, KR-DH, observed in one of the type-I PKSs is known to be specific for PksE. Therefore, the product of pks/nrps-7 will include an enediyne moiety [39].
3.4. Specificity of the PKS and NRPS Gene Clusters in Each Strain
We conducted a BLAST search to investigate whether the gene clusters identified in this study are specific in each strain or present in the other strains. All the PKSs and NRPSs of M. humidisoli AKA109 were also present in M. humidisoli MMS20-R2-29T (Table 3). As the TPA0907_16820 homolog in M. humidisoli MMS20-R2-29T is not well sequenced, it was not hit in the search. Although a homolog of TPA0907_20190 was also present in M. humidisoli MMS20-R2-29T, it is not described in the table because its sequence identity/similarity were lower (99/98 in%) than those of Micromonospora sp. RL09-050-HVF-A.
Among eleven gene clusters of Micromonospora sp. AKA38, seven (t1pks-8, t2pks-2, t3pks-1, pks/nrps-2, pks/nrps-4, pks/nrps-5 and pks/nrps-7) were present in other strains with high sequence identity/similarity, although TPA0908_54560, TPA0908_54550 and TPA0908_54470 in pks/nrps-7 were not observed, suggesting pks/nrps-7 orthologs in other strains may be partial or not completely sequenced. Except for pks/nrps-4, the closest genes were present in Micromonospora sp. RP3T and their identity/similarity values were quite high. In contrast, four gene clusters, t1pks-7, nrps-4, nrps-5 and pks/nrps-6, were not present in other strains because their BLAST top hits showed low identity/similarity values. This suggests that they are novel and specific to strain AKA38.
4. Discussion
Many strains found as producers of new bioactive substances have not been classified yet at species level. Consequently, relationships between products and taxonomic positions of the producer are not well understood. In this study, we classified Micromonospora sp. AKA109, a producer of akazaoxime and A-76356, to M. humidisoli [40]. In contrast, Micromonospora sp. AKA38, a producer of levantilide C, was revealed to be a novel genomospecies. If Micromonospora sp. AKA38 is characterized in detail [41], it can be proposed as a new Micromonospora species because it was not classified to known species. M. humidisoli is very recently proposed, and its type strain, MMS20-R2-29T, was isolated from riverside soil. It is explained that its growth occurs in the presence of 0–2% NaCl, with optimal growth at 0% NaCl [40]. In contrast, strain AKA109 was isolated from deep sea water with a higher salt concentration. To the best of our knowledge, this is the first report on marine-derived M. humidisoli.
Recently, genome mining has often been used when searching for new compounds. However, if researchers find an unknown BGC that appears novel by genome mining, it may be a BGC for known compounds, because many BGCs of known compounds have not been identified, and consequently, they are considered BGCs for new compounds. Thus, BGCs of known compounds need to be identified for more effective genome mining if the BGCs have not been unidentified. We here identified the BGC of akazaoxime and A-76356, and that of levantilide C from Micromonospora sp. AKA109 and Micromonospora sp. AKA38, respectively. This is the first report on the BGCs and biosynthetic pathways of these compounds.
Micromonospora sp. AKA109, classified to M. humidisoli, harbored fourteen PKS and NRPS gene clusters, all of which are also present in M. humidisoli MMS20-R2-29T. This well supports our idea that members of the same species possess similar sets of PKS and NRPS gene clusters [42,43,44]. Micromonospora sp. AKA38, classified as a new genomospecies, harbored eleven PKS and NRPS gene clusters. Although seven of them were present in other strains, such as Micromonospora sp. RP3T and Micromonospora sp. WMMA2032, the remaining four are not found in any other strains. If a strain is taxonomically novel at the species level, it may possess new PKS and/or NRPS gene clusters.
Although PKS and NRPS gene clusters found from our two strains include BGCs of known compounds such as amycomicin, alkyl-O-dihydrogeranyl-methoxyhydroquinone and quinolidomicin, and congeners of known compounds, they include many orphan and unknown clusters. Their products were predicted to be novel at present. Thus, these two strains are expected to produce new and diverse polyketide and non-ribosomal peptide compounds.
Except for PKS and NRPS gene clusters, eleven putative secondary metabolite-biosynthetic gene clusters are present in each genome of M. humidisoli AKA109 and Micromonospora sp. AKA38 (Tables S1 and S2). The products, except for SapB, desferrioxamine, N-acetylglutaminylglutamine amide (NAGGN) and class II lanthipeptides of Micromonospora sp. AKA38, could not be predicted because there is less information on these types of gene clusters. SapB, desferrioxamine, NAGGN, three terpene, and one hybrid oligosaccharide/terpene gene cluster are conserved in the two strains. SapB, desferrioxamine and NAGGN are known as common secondary metabolites in actinomycetes. The numbers of gene clusters shown in Tables S1 and S2 did not exceed those of the PKS and NRPS gene clusters (Table 1 and Table 2). This supports the assertion that polyketides and non-ribosomal peptides are major and diverse secondary metabolites, as previously reported [18].
5. Conclusions
We sequenced whole genomes of an akazaoxime- and A-76356-producer, Micromonospora sp. AKA109, and a levantilide C-producer, Micromonospora sp. AKA38. Micromonospora sp. AKA109 was identified as M. humidisoli, whereas Micromonospora sp. AKA38 was revealed to be a new genomospecies. Akazaoxime- and A-76356-BGC and levantilide C-one were identified from whole genome sequences of these two strains, respectively. M. humidisoli AKA109 harbored fourteen PKS and NRPS gene clusters, all of which were conserved in the type strain of M. humidisoli. Micromonospora sp. AKA38 harbored eleven PKS and NRPS gene clusters. Our bioinformatic analysis suggested their potential to synthesis diverse non-ribosomal peptides and polyketides.
Supplementary Materials
The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/life13020542/s1, Table S1: Secondary metabolite-biosynthetic gene clusters, except for PKS and NRPS gene clusters, of M. humidisoli AKA109; Table S2: Secondary metabolite-biosynthetic gene clusters, except for PKS and NRPS gene clusters, of Micromonospora sp. AKA38.
Author Contributions
Conceptualization, H.K. and Y.I., methodology, T.T., resources, Y.I., data curation, H.K., writing—original draft preparation, H.K., writing—review and editing, Y.I., project administration, T.T. and Y.I., funding acquisition, T.T. All authors have read and agreed to the published version of the manuscript.
Funding
This research was supported in part by a commissioned project from the Japan Patent Office.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
The whole genome shotgun project of Micromonospora sp. AKA109 and Micromonospora sp. AKA38 have been deposited at GenBank under the accession numbers BNEH00000000 and BNEI00000000, respectively. BioProject accession numbers are PRJDB9818 and PRJDB9819. BioSample accession numbers are SAMD00228008 and SAMD00228009.
Acknowledgments
We thank Shinpei Ino and Takahiro Matsuyama for genome DNA preparation and Aya Uohara for registering whole genome sequences in DDBJ.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Berdy, J. Bioactive microbial metabolites. J. Antibiot. 2005, 58, 1–26. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Harunari, E.; Imada, C.; Igarashi, Y.; Fukuda, T.; Terahara, T.; Kobayashi, T. Hyaluromycin, a new hyaluronidase inhibitor of polyketide origin from marine Streptomyces sp. Mar. Drugs 2014, 12, 491–507. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Igarashi, Y.; Ikeda, M.; Miyanaga, S.; Kasai, H.; Shizuri, Y.; Matsuura, N. Two butenolides with PPARα agonistic activity from a marine-derived Streptomyces. J. Antibiot. 2015, 68, 345–347. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Igarashi, Y.; Shimasaki, R.; Miyanaga, S.; Oku, N.; Onaka, H.; Sakurai, H.; Saiki, I.; Kitani, S.; Nihira, T.; Wimonsiravude, W.; et al. Rakicidin D, an inhibitor of tumor cell invasion from marine-derived Streptomyces sp. J. Antibiot. 2010, 63, 563–565. [Google Scholar] [CrossRef] [PubMed]
- Igarashi, Y.; Zhou, T.; Sato, S.; Matsumoto, T.; Yu, L.; Oku, N. Akaeolide, a carbocyclic polyketide from marine-derived Streptomyces. Org. Lett. 2013, 15, 5678–5681. [Google Scholar] [CrossRef] [PubMed]
- Karim, M.R.U.; In, Y.; Zhou, T.; Harunari, E.; Oku, N.; Igarashi, Y. Nyuzenamides A and B: Bicyclic peptides with antifungal and cytotoxic activity from a marine-derived Streptomyces sp. Org. Lett. 2021, 23, 2109–2113. [Google Scholar] [CrossRef] [PubMed]
- Kim, Y.; Ogura, H.; Akasaka, K.; Oikawa, T.; Matsuura, N.; Imada, C.; Yasuda, H.; Igarashi, Y. Nocapyrones: Alpha- and gamma-pyrones from a marine-derived Nocardiopsis sp. Mar. Drugs 2014, 12, 4110–4125. [Google Scholar] [CrossRef] [Green Version]
- Yang, T.; Yamada, K.; Zhou, T.; Harunari, E.; Igarashi, Y.; Terahara, T.; Kobayashi, T.; Imada, C. Akazamicin, a cytotoxic aromatic polyketide from marine-derived Nonomuraea sp. J. Antibiot. 2019, 72, 202–209. [Google Scholar] [CrossRef]
- Zhang, Z.; Zhou, T.; Yang, T.; Fukaya, K.; Harunari, E.; Saito, S.; Yamada, K.; Imada, C.; Urabe, D.; Igarashi, Y. Nomimicins B-D, new tetronate-class polyketides from a marine-derived actinomycete of the genus Actinomadura. Beilstein J. Org. Chem. 2021, 17, 2194–2202. [Google Scholar] [CrossRef]
- Qi, S.; Gui, M.; Li, H.; Yu, C.; Li, H.; Zeng, Z.; Sun, P. Secondary metabolites from marine Micromonospora: Chemistry and bioactivities. Chem. Biodivers 2020, 17, e2000024. [Google Scholar] [CrossRef]
- Yan, S.; Zeng, M.; Wang, H.; Zhang, H. Micromonospora: A prolific source of bioactive secondary metabolites with therapeutic potential. J. Med. Chem. 2022, 65, 8735–8771. [Google Scholar] [CrossRef] [PubMed]
- Igarashi, Y.; Matsuyuki, Y.; Yamada, M.; Fujihara, N.; Harunari, E.; Oku, N.; Karim, M.R.U.; Yang, T.; Yamada, K.; Imada, C.; et al. Structure determination, biosynthetic origin, and total synthesis of akazaoxime, an enteromycin-class metabolite from a marine-derived actinomycete of the genus Micromonospora. J. Org. Chem. 2021, 86, 6528–6537. [Google Scholar] [CrossRef]
- Fei, P.; Chuan-Xi, W.; Yang, X.; Hong-Lei, J.; Lu-Jie, C.; Uribe, P.; Bull, A.T.; Goodfellow, M.; Hong, J.; Yun-Yang, L. A new 20-membered macrolide produced by a marine-derived Micromonospora strain. Nat. Prod. Res. 2013, 27, 1366–1371. [Google Scholar] [CrossRef]
- Fischbach, M.A.; Walsh, C.T. Assembly-line enzymology for polyketide and nonribosomal peptide antibiotics: Logic, machinery, and mechanisms. Chem. Rev. 2006, 106, 3468–3496. [Google Scholar] [CrossRef] [PubMed]
- Schwarzer, D.; Marahiel, M.A. Multimodular biocatalysts for natural product assembly. Naturwissenschaften 2001, 88, 93–101. [Google Scholar] [CrossRef] [PubMed]
- Zhan, J. Biosynthesis of bacterial aromatic polyketides. Curr. Top Med. Chem. 2009, 9, 1598–1610. [Google Scholar] [CrossRef] [PubMed]
- Katsuyama, Y.; Ohnishi, Y. Type III polyketide synthases in microorganisms. Methods Enzym. 2012, 515, 359–377. [Google Scholar]
- Nett, M.; Ikeda, H.; Moore, B.S. Genomic basis for natural product biosynthetic diversity in the actinomycetes. Nat. Prod. Rep. 2009, 26, 1362–1384. [Google Scholar] [CrossRef]
- Komaki, H.; Ichikawa, N.; Oguchi, A.; Hamada, M.; Harunari, E.; Kodani, S.; Fujita, N.; Igarashi, Y. Draft genome sequence of Streptomyces sp. TP-A0867, an alchivemycin producer. Stand Genomic. Sci. 2016, 11, 85. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Yoon, S.; Ha, S.; Kwon, S.; Lim, J.; Kim, Y.; Seo, H.; Chun, J. Introducing EzBioCloud: A taxonomically united database of 16S rRNA gene sequences and whole-genome assemblies. Int. J. Syst. Evol. Microbiol. 2017, 67, 1613–1617. [Google Scholar] [CrossRef] [PubMed]
- Komaki, H.; Igarashi, Y.; Tamura, T. Taxonomic positions of a nyuzenamide-producer and its closely related strains. Microorganisms 2022, 10, 349. [Google Scholar] [CrossRef]
- Meier-Kolthoff, J.P.; Göker, M. TYGS is an automated high-throughput platform for state-of-the-art genome-based taxonomy. Nat. Commun. 2019, 10, 2182. [Google Scholar] [CrossRef] [Green Version]
- Meier-Kolthoff, J.P.; Auch, A.F.; Klenk, H.P.; Göker, M. Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinform. 2013, 14, 60. [Google Scholar] [CrossRef] [Green Version]
- Blin, K.; Shaw, S.; Steinke, K.; Villebro, R.; Ziemert, N.; Lee, S.Y.; Medema, M.H.; Weber, T. antiSMASH 5.0: Updates to the secondary metabolite genome mining pipeline. Nucleic Acids Res. 2019, 47, W81–W87. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Hatano, K.; Nishii, T.; Kasai, H. Taxonomic re-evaluation of whorl-forming Streptomyces (formerly Streptoverticillium) species by using phenotypes, DNA-DNA hybridization and sequences of gyrB, and proposal of Streptomyces luteireticuli (ex Katoh and Arai 1957) corrig., sp. nov., nom. rev. Int. J. Syst. Evol. Microbiol. 2003, 53, 1519–1529. [Google Scholar] [CrossRef] [PubMed]
- Kasai, H.; Tamura, T.; Harayama, S. Intrageneric relationships among Micromonospora species deduced from gyrB-based phylogeny and DNA relatedness. Int. J. Syst. Evol. Microbiol. 2000, 50, 127–134. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Meier-Kolthoff, J.P.; Goker, M.; Sproer, C.; Klenk, H.P. When should a DDH experiment be mandatory in microbial taxonomy? Arch Microbiol. 2013, 195, 413–418. [Google Scholar] [CrossRef] [PubMed]
- Stackebrandt, E.; Ebers, J. Taxonomic parameters revisited: Tarnished gold standards. Microbiol. Today 2006, 33, 152–155. [Google Scholar]
- Wayne, L.G.; Brenner, D.J.; Colwell, R.R.; Grimont, P.A.D.; Kandler, O.; Krichevsky, M.I.; Moore, B.S.; Moore, W.E.; Murray, R.G.E.; Stackebrandt, E.; et al. Report of the ad hoc committee on reconciliation of approaches to bacterial systematics. Int. J. Syst. Bacteriol. 1987, 37, 463–464. [Google Scholar] [CrossRef] [Green Version]
- Hong, S.; Ban, Y.H.; Byun, W.S.; Kim, D.; Jang, Y.; An, J.S.; Shin, B.; Lee, S.K.; Shin, J.; Yoon, Y.J.; et al. Camporidines A and B: Antimetastatic and anti-inflammatory polyketide alkaloids from a gut bacterium of Camponotus kiusiuensis. J. Nat. Prod. 2019, 82, 903–910. [Google Scholar] [CrossRef] [PubMed]
- Ohno, S.; Katsuyama, Y.; Tajima, Y.; Izumikawa, M.; Takagi, M.; Fujie, M.; Satoh, N.; Shin-ya, K.; Ohnishi, Y. Identification and characterization of the streptazone E biosynthetic gene cluster in Streptomyces sp. MSC090213JE08. ChemBioChem 2015, 16, 2385–2391. [Google Scholar] [CrossRef]
- Ye, S.; Molloy, B.; Brana, A.F.; Zabala, D.; Olano, C.; Cortes, J.; Moris, F.; Salas, J.A.; Mendez, C. Identification by genome mining of a type I polyketide gene gluster from Streptomyces argillaceus involved in the biosynthesis of pyridine and piperidine alkaloids argimycins P. Front. Microbiol. 2017, 8, 194. [Google Scholar] [CrossRef]
- Liang, M.; Liu, L.; Xu, F.; Zeng, X.; Wang, R.; Yang, J.; Wang, W.; Karthik, L.; Liu, J.; Yang, Z.; et al. Activating cryptic biosynthetic gene cluster through a CRISPR-Cas12a-mediated direct cloning approach. Nucleic Acids Res. 2022, 50, 3581–3592. [Google Scholar] [CrossRef] [PubMed]
- Awakawa, T.; Fujita, N.; Hayakawa, M.; Ohnishi, Y.; Horinouchi, S. Characterization of the biosynthesis gene cluster for alkyl-O-dihydrogeranyl-methoxyhydroquinones in Actinoplanes missouriensis. ChemBioChem 2011, 12, 439–448. [Google Scholar] [CrossRef] [PubMed]
- He, H.Y.; Ryan, K.S. Glycine-derived nitronates bifurcate to O-methylation or denitrification in bacteria. Nat. Chem. 2021, 13, 599–606. [Google Scholar] [CrossRef]
- Cortina, N.S.; Revermann, O.; Krug, D.; Muller, R. Identification and characterization of the althiomycin biosynthetic gene cluster in Myxococcus xanthus DK897. ChemBioChem 2011, 12, 1411–1416. [Google Scholar] [CrossRef] [PubMed]
- Hashimoto, T.; Hashimoto, J.; Kozone, I.; Amagai, K.; Kawahara, T.; Takahashi, S.; Ikeda, H.; Shin-ya, K. Biosynthesis of quinolidomicin, the largest known macrolide of terrestrial origin: Identification and heterologous expression of a biosynthetic gene cluster over 200 kb. Org. Lett. 2018, 20, 7996–7999. [Google Scholar] [CrossRef] [PubMed]
- Komaki, H.; Ichikawa, N.; Hosoyama, A.; Hamada, M.; Igarashi, Y. In silico analysis of PKS and NRPS gene clusters in arisostatin- and kosinostatin-producers and description of Micromonospora okii sp. nov. Antibiotics 2021, 10, 1447. [Google Scholar] [CrossRef]
- Horsman, G.P.; Van Lanen, S.G.; Shen, B. Iterative type I polyketide synthases for enediyne core biosynthesis. Methods Enzymol. 2009, 459, 97–112. [Google Scholar]
- Lee, D.H.; Ra, J.S.; Kim, M.J.; Kim, S.B. Micromonospora antibiotica sp. nov. and Micromonospora humidisoli sp. nov., two new actinobacterial species exhibiting antimicrobial potential. Int. J. Syst. Evol. Microbiol. 2022, 72, 005522. [Google Scholar] [CrossRef]
- Chun, J.; Oren, A.; Ventosa, A.; Christensen, H.; Arahal, D.R.; da Costa, M.S.; Rooney, A.P.; Yi, H.; Xu, X.W.; De Meyer, S.; et al. Proposed minimal standards for the use of genome data for the taxonomy of prokaryotes. Int. J. Syst. Evol. Microbiol. 2018, 68, 461–466. [Google Scholar] [CrossRef] [PubMed]
- Komaki, H.; Sakurai, K.; Hosoyama, A.; Kimura, A.; Igarashi, Y.; Tamura, T. Diversity of nonribosomal peptide synthetase and polyketide synthase gene clusters among taxonomically close Streptomyces strains. Sci. Rep. 2018, 8, 6888. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Komaki, H.; Tamura, T. Reclassification of Streptomyces diastaticus subsp. ardesiacus, Streptomyces gougerotii and Streptomyces rutgersensis. Int. J. Syst. Evol. Microbiol. 2020, 70, 4291–4297. [Google Scholar] [CrossRef]
- Komaki, H.; Tamura, T. Differences at species level and in repertoires of secondary metabolite biosynthetic gene clusters among Streptomyces coelicolor A3(2) and type strains of S. coelicolor and its taxonomic neighbors. Appl. Microbiol. 2021, 1, 573–585. [Google Scholar] [CrossRef]
Figure 1.
Chemical structures of akazaoxime (1), A-76356 (2) and levantilide C (3).
Figure 2.
Phylogenetic tree based on 16S rRNA gene sequences. Type strains of species showing sequence simiralities of >99.0% to Micromonospora sp. AKA109 and/or Micromonospora AKA38 are included in this tree. Numbers on the branches are the confidence limits estimated by bootstrap analysis with 1000 replicates, and values above 50% are indicated at branching points. Phytohabitans suffuscus K07-0523T (AB490769) was used as an outgroup (not shown).
Figure 2.
Phylogenetic tree based on 16S rRNA gene sequences. Type strains of species showing sequence simiralities of >99.0% to Micromonospora sp. AKA109 and/or Micromonospora AKA38 are included in this tree. Numbers on the branches are the confidence limits estimated by bootstrap analysis with 1000 replicates, and values above 50% are indicated at branching points. Phytohabitans suffuscus K07-0523T (AB490769) was used as an outgroup (not shown).
Figure 3.
Phylogenetic tree based on gyrB sequences. Type strains of species shown in Figure 2 are included in this tree. Numbers on the branches are the confidence limits estimated by bootstrap analysis with 1000 replicates, and values above 50% are indicated at branching points. P. suffuscus NBRC 105367T (AP022871) was used as an outgroup (not shown).
Figure 3.
Phylogenetic tree based on gyrB sequences. Type strains of species shown in Figure 2 are included in this tree. Numbers on the branches are the confidence limits estimated by bootstrap analysis with 1000 replicates, and values above 50% are indicated at branching points. P. suffuscus NBRC 105367T (AP022871) was used as an outgroup (not shown).
Figure 4.
Phylogenomic tree reconstituted using the TYGS server. P. suffuscus NBRC 105367T (AP022871) was used as an outgroup (not shown) to show the root. The numbers in parentheses are accession numbers of WGS Projects or whole genome sequences in GenBank. Type strains of species shown in Figure 2 whose whole genome sequences are published are included in this tree.
Figure 4.
Phylogenomic tree reconstituted using the TYGS server. P. suffuscus NBRC 105367T (AP022871) was used as an outgroup (not shown) to show the root. The numbers in parentheses are accession numbers of WGS Projects or whole genome sequences in GenBank. Type strains of species shown in Figure 2 whose whole genome sequences are published are included in this tree.
Figure 5.
Putative biosynthetic pathways for akazaoxime (1) and A-76356 (2). An intermediate converted by the diiron oxygenase is shown in gray.
Figure 5.
Putative biosynthetic pathways for akazaoxime (1) and A-76356 (2). An intermediate converted by the diiron oxygenase is shown in gray.
Figure 6.
Proposed biosynthetic pathway of levantilide C (3). Abbreviations of domains are the same as those in Table 1. dh, inactive DH; er, inactive ER.
Figure 6.
Proposed biosynthetic pathway of levantilide C (3). Abbreviations of domains are the same as those in Table 1. dh, inactive DH; er, inactive ER.
Table 1.
PKS and NRPS gene clusters in the whole genome of M. humidisoli AKA109.
| Cluster | Locus Tag (TPA0907) | Domain Organization | Product Predicted |
|---|---|---|---|
| t1pks-1 | _14850 _14840 _14830 | KS ATm ACP KS ATm DH KR ACP KS ATm DH KR ACP KS ATm DH KR ACP KS ATm DH ACP KS ATmm DH KR ACP TD | New analog(s) of camporidine, argimycin, streptazone |
| t1pks-2 | _16830 _16820 _16810 | KS ATm ACP ACP ACP KR KS ATmm ACP | Unknown |
| t1pks-3 | _18400 _18690 | KS AT DH KR ACP KS ATm KR DH | Compound with an enediyne moiety |
| t1pks-4 | _47680 | KS ATm DH ER KR ACP | Unknown |
| t1pks-5 (mrl) | _35900 _35890 _35880 _35870 _35750 | KS ATm DH KR ACP KS ATm KR ACP KS ATm KR ACP KS ATmm KR ACP KS ATm DH KR ACP KS ATm DH KR ACP KS ATm DH KR ACP TE ACP KS ATm DH KR ACP KS ATmm DH KR ACP KS ATmm DH KR ACP KS ATm DH KR ACP | Marinolactam congener |
| t1pks-6 | _29310 | KS ATm DH ER KR ACP | Amycomicin |
| t2pks-1 | _20160 _20170 _20190 | KSα KSβ (CLF) ACP | Aromatic polyketide |
| t3pks-1 * (aqq) | _59200 | KS | Alkyl-O-dihydrogeranyl-methoxyhydroquinone |
| nrps-1 | _47220 _47230 _47240 | C Aphe PCP C A PCP C | Phe-x |
| nrps-2 | _47680 | A PCP C | Unknown |
| nrps-3 | _56920 _56930 _56940 _56970 C | C A PCP C Acys PCP A PCP C C Aglu PCP E C | Tetrapeptide including Cys and Glu |
| pks/nrps-1 | _15480 | TE A PCP KS ATm KR ACP | Unknown |
| pks/nrps-2 * | _28040 _28030 _28010 _28000 _27970 _27960 | A PCP KS TE A PCP C PCP KS ATm KR DH ACP C Aasn PCP C Aser PCP TE | x-x-y-mal-Asn-Ser |
| pks/nrps-3 | _56660 _56670 _56710 _56840 C | A PCP KS ATm KR ACP ACP C Aleu PCP | Akazaoxime and A-76356 |
C, encoded in the complementary strand; *, conserved between strains AKA109 and AKA38; A, adenylation domain; ACP, acyl carrier protein; AT, acyltransferase domain; ATm, AT for malonyl-CoA, ATmm, AT for methylmalonyl-CoA; ATem/mx, AT for ethylmalonyl-CoA or methoxymalonyl CoA; C, condensation domain; CLF, chain length factor; CoL, CoA ligase domain; DH, dehydratase domain; Cyc, cyclase domain; E, epimerization domain; ER, enoylreductase domain; KR, ketoreductase domain; KS, ketosynthase domain; mal, residue derived from malonyl-CoA; MT, methyltransferase domain; nrps, PCP, peptidyl carrier protein; nrps, NRPS gene; pks/nrps, hybrid PKS/NRPS gene; pk, residue derived from a single module of type-I PKS; TD, termination domain; TE, thioesterase domain, t1pks, type-I PKS gene; t2pks, type-II PKS gene; t3pks, type-III PKS gene; x, unidentified amino acid residue; y, unknown unit by lack of A domain in the module. Amino acids incorporated by A domains are indicated as 3-letter abbreviations in subscript just after A.
Table 2.
PKS and NRPS gene clusters in the whole genome of Micromonospora sp. AKA38.
| Gene Cluster | Locus Tag (TPA0908) | Domain Organization | Product Predicted |
|---|---|---|---|
| t1pks-7 | _40860 _40870 _40880 | ATmm ACP KS ATm KR ACP KS ATm DH ER KR ACP KS ATmm DH ER KR ACP KS ATmm DH ER KR ACP KS ATmm DH KR ACP KS ATmm DH ER KR ACP KS ATmm KR ACP KS ATm DH KR ACP KS ATm KR ACP KS ATm DH KR ACP KS ATm DH KR ACP TE | Levantilide C |
| t1pks-8 (qmn) | _45370 _45410 _45420 _45440 _45450 _45460 _45470 _45480 _45490 _45500 _45510 _45520 _45530 | CoL ACP KS ATm DH KR ACP KS ATmm DH ER KR ACP KS ATm DH KR ACP KS ATm KR ACP KS ATm KR ACP KS ATm KR ACP KS ATm DH ER KR ACP KS ATmm DH ER KR ACP KS ATm DH ER KR ACP KS ATm KR ACP KS AT KR ACP KS ATm DH KR ACP KS ATm DH KR ACP KS ATm DH KR ACP KS ATm KR ACP KS ATm KR ACP KS ATm KR ACP KS ATmm DH KR ACP KS ATm DH KR ACP KS ATmm KR ACP KS ATm KR ACP KS ATmm KR ACP KS ATmm DH ER KR ACP KS ATm KR ACP KS ATmm KR ACP KS ATmm KR ACP KS ATm DH KR ACP KS ATmm DH KR ACP KS ATmm KR ACP KS ATmm KR ACP KS ATm KR ACP KS ATm KR ACP TE | Quinolidomicin |
| t2pks-2 | _49930 _49910 _49900 | ACP Cyc KSα KSβ (CLF) | Unknown |
| t3pks-1 * (aqq) | _06420 | KS | Alkyl-O-dihydrogeranyl-methoxyhydroquinone |
| nrps-4 | _34180 _34160 _34150 _34130 _34100 | Athr MT PCP C Apro PCP C PCP C PCP TE TE Aval PCP A C Athr PCP C Aleu PCP C Apro PCP C Aleu PCP C | Val-Thr-Leu-Pro-Leu-mThr-Pro-y-y |
| nrps-5 | _34870 C _34920 _35060 _35080 | C A PCP C A PCP C Aasn PCP TE A PCP C Aasn PCP C A PCP C Athr PCP C Aasn PCP C A PCP C A PCP C Athr PCP C A PCP TE | x-Asn-x-Thr-Asn-x-x-Thr-x-x-x-Asn |
| pks/nrps-2 * | _42740 _42750 _42770 _42780 _42810 _42820 | A PCP KS TE A PCP C PCP KS ATm KR DH ACP C Aasn PCP C Aser PCP TE | x-x-y-mal-Asn-Ser |
| pks/nrps-4 | _08330 _08340 _08370 | C Aasn PCP KS ATm ACP C A PCP Aala PCP C Aglu PCP C PCP | Asn-mal-x-Ala-Glu-y |
| pks/nrps-5 | _34600 _34620 _34650 _34660 _34670 _34690 _34690 _34730 | TE A PCP A PCP KS A PCP C PCP KS ATm KR ACP C Aser PCP PCP | x-x-x-y-mal-Ser |
| pks/nrps-6 | _35130 _35200 _35210 _35230 C _35250 C | Athr PCP A PCP C Aasn PCP ACP KS AT DH KR ACP C A PCP C | x-Thr-x-Asn-pk |
| pks/nrps-7 | _54560 C _54550 C _54470 C _54430 C _54260 _54200 _54120 _54020 C _54000 _53990 _53970 | C A PCP PCP C A Aala PCP C Aval PCP KS (type III PKS) KS ATm KR DH PCP TE C Aval PCP KS ATm ACP Aser | Ala-Val-enediyne-Val-mal-Ser-x-x with an aromatic moiety |
Footnotes are the same as those of Table 1.
Table 3.
The closest homolog or ortholog of PKSs and NRPSs encoded by the gene clusters of M. humidisoli AKA109 and Micromonospora sp. AKA38.
Table 3.
The closest homolog or ortholog of PKSs and NRPSs encoded by the gene clusters of M. humidisoli AKA109 and Micromonospora sp. AKA38.
| Cluster | Locus Tag (TPA090) | BLAST Top Hit | ||
|---|---|---|---|---|
| I/S (%) 1 | Locus Tag or Gene (Accession No.) | Origin | ||
| t1pks-1 | 7_14850 7_14840 7_14830 | 99/99 99/99 99/99 | JQN84_27510 JQN84_31080 JQN84_29090 | M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T |
| t1pks-2 | 7_16830 7_16820 7_16810 | 90/92 99/99 100/100 | J7462_RS07410 JQN84_30180 JQN84_30185 | Micromonospora sp. RL09-050-HVF-A M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T |
| t1pks-3 | 7_18400 7_18690 | 99/100 99/100 | JQN84_22230 JQN84_22370 | M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T |
| t1pks-4 | 7_47680 | 99/99 | JQN84_24840 | M. humidisoli MMS20-R2-29T |
| t1pks-5 (mrl) | 7_35900 7_35890 7_35880 7_35870 7_35750 | 99/99 99/99 99/99 99/99 99/99 | JQN84_05260 JQN84_05265 JQN84_05270 JQN84_05275 JQN84_05335 | M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T |
| t1pks-6 | 7_29310 | 99/100 | JQN84_14785 | M. humidisoli MMS20-R2-29T |
| t2pks-1 | 7_20160 7_20170 7_20190 | 99/100 99/99 99/100 | JQN84_23105 JQN84_23110 J7462_05705 | M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T Micromonospora sp. RL09-050-HVF-A |
| t3pks-1 * (aqq) | 7_59200 | 100/100 | JQN84_06220 | M. humidisoli MMS20-R2-29T |
| nrps-1 | 7_47220 7_47230 7_47240 | 99/99 99/99 99/100 | JQN84_30545 JQN84_30550 JQN84_30555 | M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T |
| nrps-2 | 7_47680 | 99/99 | JQN84_14135 | M. humidisoli MMS20-R2-29T |
| nrps-3 | 7_56920 7_56930 7_56940 7_56970 | 99/100 99/99 99/99 99/99 | JQN84_29450 JQN84_29445 JQN84_29440 JQN84_29425 | M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T |
| pks/nrps-1 | 7_15480 | 99/99 | JQN84_27845 | M. humidisoli MMS20-R2-29T |
| pks/nrps-2 * | 7_28040 7_28030 7_28010 7_28000 7_27970 7_27960 | 99/99 99/99 99/99 99/99 98/98 99/99 | JQN84_25460 JQN84_25465 JQN84_25475 JQN84_25480 JQN84_25495 JQN84_25500 | M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T |
| pks/nrps-3 | 7_56660 7_56670 7_56710 7_56840 | 99/99 99/99 100/100 99/99 | JQN84_29575 JQN84_29570 JQN84_29550 JQN84_29485 | M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T M. humidisoli MMS20-R2-29T |
| t1pks-7 | 8_40860 8_40870 8_40880 | 59/69 56/67 54/66 | C8E87_8689 M4V62_39485 SBI_01382 | Actinoplanes brasiliensis DSM 43805T Streptomyces durmitorensis MS405 “Streptomyces bingchenggensis” BCW-1 |
| t1pks-8 (qmn) | 8_45370 8_45410 8_45420 8_45440 8_45450 8_45460 8_45470 8_45480 8_45490 8_45500 8_45510 8_45520 8_45530 | 98/98 96/96 95/96 91/93 91/93 97/98 98/98 97/97 94/95 97/98 99/99 96/96 96/97 | C8054_25705 C8054_25725 C8054_25730 H1D33_RS20350 H1D33_20360 C8054_27580 C8054_27585 C8054_27590 H1D33_20380 C8054_11295 C8054_11300 C8054_11305 C8054_11310 | Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T M. ferruginea 28ISP2-46 M. ferruginea 28ISP2-46 Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T M. ferruginea 28ISP2-46 Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T |
| t2pks-2 | 8_49930 8_49910 8_49900 | 98/99 99/99 99/99 | C8054_23750 CO540_02355 C8054_23735 | Micromonospora sp. RP3T Micromonospora sp. WMMA2032 Micromonospora sp. RP3T |
| t3pks-1 * (aqq) | 8_06420 | 99/98 | C8054_27190 | Micromonospora sp. RP3T |
| nrps-4 | 8_34180 8_34160 8_34150 8_34130 8_34100 | 55/66 63/73 55/65 53/66 51/64 | ADL15_RS07780 bnvE (QVQ62850) HUV60_15065 Raf01_61150 HUV60_15130 | “Actinoplanes awajinensis subsp. mycoplanecinus” NRRL B-16712 Streptomyces sp. UTZ13 Streptomyces sp. KMM 9044 Rugosimonospora africana NBRC 104875T Streptomyces sp. KMM 9044 |
| nrps-5 | 8_34870 C 8_34920 8_35060 8_35080 | 42/58 44/57 55/67 54/68 | KA716_28265 HRW08_08145 SAMN05216553 _119106 DMC61_21850 | Gloeotrichia echinulata DEX184 Streptomyces lunaelactis MM15 Lentzea fradiae CGMCC 4.3506T Amycolatopsis sp. WAC 04169 |
| pks/nrps-2 * | 8_42740 8_42750 8_42770 8_42780 8_42810 8_42820 | 99/99 97/97 98/98 99/99 96/96 99/99 | C8054_04550 C8054_04555 C8054_04565 C8054_04570 C8054_04585 C8054_04590 | Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T |
| pks/nrps-4 | 8_08330 8_08340 8_08370 | 87/88 86/88 87/90 | GA0070213 _12115 CO540_09565 CO540_09580 | M. humi DSM 45647T Micromonospora sp. WMMA2032 Micromonospora sp. WMMA2032 |
| pks/nrps-5 | 8_34600 8_34620 8_34650 8_34660 8_34670 8_34690 8_34690 8_34730 | 98/98 98/98 96/96 95/96 97/98 97/97 97/97 99/98 | C8054_08855 C8054_08865 C8054_08880 C8054_08885 C8054_08890 C8054_08900 C8054_08905 C8054_08920 | Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T |
| pks/nrps-6 | 8_35130 8_35200 8_35210 8_35230 8_35250 | 52/59 59/69 55/70 64/73 56/68 | GCM10011578 _091720 MXD61_11230 LX86_002128 SAMN05216215 _102899 SAMN05216215 _102897 | Streptomyces fuscichromogenes CGMCC 4.7110T Frankia sp. AgPm24 Lentzea aerocolonigenes DSM 40034T Saccharopolyspora shandongensis CGMCC 4.3530T S. shandongensis CGMCC 4.3530T |
| pks/nrps-7 | 8_54560 8_54550 8_54470 8_54430 8_54260 8_54200 8_54120 8_54020 8_54000 8_53990 8_53970 | 63/76 71/82 57/69 89/94 94/95 89/92 93/95 98/98 96/97 98/98 98/98 | Psuf_070260 Psuf_070270 FHG89_16340 DER29_6205 C8054_02625 DLJ59_18505 C8054_02645 C8054_02695 C8054_02705 C8054_02710 C8054_02715 | Phytohabitans suffuscus NBRC 105367T P. suffuscus NBRC 105367T M. orduensis S2509 Micromonospora sp. M71_S20 Micromonospora sp. RP3T M. inaquosa LB39T Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T Micromonospora sp. RP3T |
1 Similarity/identity in amino acid sequences. C, encoded in the complementary strand; *, conserved between strains AKA109 and AKA38.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2023 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
MDPI and ACS Style
Komaki, H.; Tamura, T.; Igarashi, Y. Taxonomic Positions and Secondary Metabolite-Biosynthetic Gene Clusters of Akazaoxime- and Levantilide-Producers. Life 2023, 13, 542. https://doi.org/10.3390/life13020542
AMA Style
Komaki H, Tamura T, Igarashi Y. Taxonomic Positions and Secondary Metabolite-Biosynthetic Gene Clusters of Akazaoxime- and Levantilide-Producers. Life. 2023; 13(2):542. https://doi.org/10.3390/life13020542
Chicago/Turabian StyleKomaki, Hisayuki, Tomohiko Tamura, and Yasuhiro Igarashi. 2023. "Taxonomic Positions and Secondary Metabolite-Biosynthetic Gene Clusters of Akazaoxime- and Levantilide-Producers" Life 13, no. 2: 542. https://doi.org/10.3390/life13020542
APA StyleKomaki, H., Tamura, T., & Igarashi, Y. (2023). Taxonomic Positions and Secondary Metabolite-Biosynthetic Gene Clusters of Akazaoxime- and Levantilide-Producers. Life, 13(2), 542. https://doi.org/10.3390/life13020542
Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.
