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Draft genome sequence of Micromonospora sp. DSW705 and distribution of biosynthetic gene clusters for depsipeptides bearing 4-amino-2,4-pentadienoate in actinomycetes
Standards in Genomic Sciences volume 11, Article number: 84 (2016)
Here, we report the draft genome sequence of Micromonospora sp. DSW705 (=NBRC 110037), a producer of antitumor cyclic depsipeptides rakicidins A and B, together with the features of this strain and generation, annotation, and analysis of the genome sequence. The 6.8 Mb genome of Micromonospora sp. DSW705 encodes 6,219 putative ORFs, of which 4,846 are assigned with COG categories. The genome harbors at least three type I polyketide synthase (PKS) gene clusters, one nonribosomal peptide synthetase (NRPS) gene clusters, and three hybrid PKS/NRPS gene clusters. A hybrid PKS/NRPS gene cluster encoded in scaffold 2 is responsible for rakicidin synthesis. DNA database search indicated that the biosynthetic gene clusters for depsipeptides bearing 4-amino-2,4-pentadienoate are widely present in taxonomically diverse actinomycetes.
In our screening of antitumor compounds from rare actinomycetes, Micromonospora sp. DSW705 collected from deep seawater was found to produce rakicidins A and B. Rakicidins are fifteen-membered cyclic depsipeptides comprising three amino acids and a modified fatty acid. The most intriguing feature of rakicidins is the presence of a rare unusual amino acid, 4-amino-2,4-pentadienoate (APDA) in their cyclic structures, which is present only in a limited range of secondary metabolites of actinomycetes [1–3]. To date, five rakicidin congeners have been reported; rakicidins A, B, and E were isolated from Micromonospora , and rakicidins C and D from Streptomyces [4–7]. Recently, we disclosed the biosynthetic gene (rak) cluster for rakicidin D through the genome analysis of Streptomyces sp. MWW064 and proposed its biosynthetic pathway . In this study, the whole genome shotgun sequencing of Micromonospora sp. DSW705 was conducted to assess its potential in secondary metabolism, to identify the biosynthetic genes for rakicidins A and B, and to make a comparative analysis with the gene cluster of rakicidin D in Streptomyces sp. MWW064. We here report the draft genome sequence of Micromonospora sp. DSW705, together with the taxonomical identification of the strain, description of its genome properties, and annotation of the rakicidin gene cluster. Furthermore, we investigated distribution of the rak–like clusters in other bacterial strains to evaluate the gene distribution in taxonomically diverse actinomycetes.
Classification and features
In the screening of antitumor compounds from rare actinomycetes, Micromonospora sp. DSW705 was isolated from deep seawater collected in Toyama Bay, Japan and found to produce BU-4664 L and rakicidins A and B (unpublished). The general feature of this strain is shown in Table 1. This strain grew well on ISP 2 and ISP 4 agars. On ISP 7 agars, the growth was poor. No growth was observed on ISP 5 agar. No aerial mycelia were observed. Substrate mycelium was orange, turning dark brown on sporulation on ISP 2 agar. No diffusible pigment was observed on ISP 2, ISP 3, ISP 4, ISP 5, ISP 6, and ISP 7 agar media. The strain bored single spore on short sporophore. The spores were spherical (0.7–0.8 μm in diameter) with wrinkle surface. A scanning electron micrograph of the strain is shown in Fig. 1. Growth occurred at 20–45 °C (optimum 37 °C) and pH 5–8 (optimum pH 7). Strain DSW705 exhibited growth with 0–3 % (w/v) NaCl (optimum 0 % NaCl). Strain DSW705 utilized arabinose, fructose, glucose, raffinose, sucrose, and xylose for growth. This strain was deposited in the NBRC culture collection with the registration number of NBRC 110037. The genes encoding 16S rRNA were amplified by PCR using two universal primers, 9 F and 1541R. After purification of the PCR product by AMPure (Beckman Coulter), the sequencing was carried out according to an established method . Homology search of the sequence by EzTaxon-e  indicated the highest similarity (99.66 %, 1448/1453) to Micromonospora chalcea DSM 43026T (X92594) as the closest type strain. A phylogenetic tree was reconstructed using ClustalX2  and NJPlot  on the basis of the 16S rRNA gene sequence together with those of taxonomically close type strains showing over 98.5 % similarities. Evolutionary distances were calculated using Kimura’s two-parameter model . The tree has been deposited into TreeBase (http://purl.org/phylo/treebase/phylows/study/TB2:S19405). In the phylogenetic tree, strain DSW705 and M. chalcea DSM 43026T (X92594) formed a monophyletic cluster with a bootstrap resampling value of 100 % (Fig. 2).
The isomer of diaminopimelic acid in the whole-cell hydrolysate was analyzed according to the method described by Hasegawa et al. . Isoprenoid quinones and cellular fatty acids were analyzed as described previously . The whole-cell hydrolysate of strain DSW705 contained meso-diaminopimelic acid as its diagnostic peptidoglycan diamino acid. The predominant menaquinone was identified as MK-10(H4); MK-9(H4), MK-10(H2), and MK-10(H6) were also detected as minor components. The major cellular fatty acids were found to be iso-C16:0, iso-C15:0 and anteiso-C17:0.
Genome sequencing information
Genome project history
In collaboration between Toyama Prefectural University and NBRC, the organism was selected for genome sequencing to elucidate the rakicidin biosynthetic pathway. The draft genome sequences have been deposited in the INSDC database under the accession number BBVA01000001-BBVA01000024. The project information and its association with MIGS version 2.0 compliance are summarized in Table 2 .
Growth conditions and genomic DNA preparation
Micromonospora sp. DSW705 was deposited in the NBRC culture collection with the registration number of NBRC 110037. The monoisolate of strain DSW705 was grown on a polycarbonate membrane filter (Advantec) on double diluted NBRC 227 agar medium (0.2 % yeast extract, 0.5 % malt extract, 0.2 % glucose, 2 % agar, pH 7.3) at 28 °C. High quality genomic DNA for sequencing was isolated from the mycelia using an EZ1 DNA Tissue Kit and a Bio Robot EZ1 (Qiagen) according to the protocol for extraction of nucleic acid from Gram-positive bacteria. The size, purity, and double-strand DNA concentration of the genomic DNA were measured by pulsed-field gel electrophoresis, ratio of absorbance values at 260 nm and 280 nm, and Quant-iT PicoGreen dsDNA Assay Kit (Life Technologies), respectively, to assess the quality of genomic DNA.
Genome sequencing and assembly
Shotgun and paired-end libraries were prepared and subsequently sequenced using 454 pyrosequencing technology and HiSeq1000 (Illumina) paired-end technology, respectively (Table 2). The 36 Mb shotgun sequences and 682 Mb paired-end sequences were assembled using Newbler v2.6 and subsequently finished using GenoFinisher  to yield 24 scaffolds larger than 500 bp. The N50 was 629,027 bp.
Coding sequences were predicted by Prodigal  and tRNA-scanSE . The gene functions were annotated by an in-house genome annotation pipeline, and searched for domains related to polyketide synthase (PKS) and nonribosomal peptide synthetase (NRPS) using the SMART and PFAM domain databases. PKS and NRPS gene clusters and their domain organizations were determined as reported previously  and using antiSMASH . Substrates of adenylation (A) and acyltransferase (AT) domains were predicted using antiSMASH. BLASTP search against the NCBI nr databases were also used for predicting function of proteins encoded in the rak cluster.
The total size of the genome is 6,795,311 bp and the GC content is 72.9 % (Table 3), similar to other genome-sequenced Micronomospora members. Of the total 6,273 genes, 6,219 are protein-coding genes and 54 are RNA genes. The classification of genes into COGs functional categories is shown in Table 4. As for secondary metabolite pathways by modular PKSs and NRPSs, Micromonospora sp. DSW705 has at least three hybrid PKS/NRPS gene clusters, three type I PKS gene clusters, and one NRPS gene clusters. According to the assembly line mechanism , we predicted the chemical structures which each cluster would synthesize (Table 5), suggesting the potential of Micromonospora sp. DSW705 to produce diverse polyketide- and nonribosomal peptide-compounds as secondary metabolites.
Insights from the genome sequence
Rakicidin biosynthetic gene cluster in Micromonospora sp. DSW705
Our previous study revealed that rakicidin is synthesized by a hybrid PKS/NRPS gene cluster. Its domain organization is shown in Fig. 3a . Among the three hybrid PKS/NRPS gene clusters present in the Micromonospora sp. DSW705 genome shown in Table 5, only pks/nrps-1 shows the same domain organization as the rak cluster of Streptomyces sp. MWW064 (Fig. 3b). Since this gene cluster encodes all the enzymes necessary for assembling the rakicidin core structure, this cluster was confirmed as a rak cluster (Table 6). Gene organizations of the clusters for rakicidin D in Streptomyces sp. MWW064 (Fig. 3a) and rakicidins A and B in Micromonospora sp. DSW705 (Fig. 3b) are essentially identical. Proposed biosynthetic pathway for rakicidins in Micromonospora sp. DSW705 is illustrated in Fig. 3b.
Biosynthetic gene clusters for rakicidins and the related compounds in other strains
Since the BLAST analysis shown in Table 6 suggests that other Micromonospora strains such as M. purpureochromogenes and Micromonospora sp. M42 may possess rak clusters, hybrid PKS/NRPS gene clusters similar to rak clusters were searched for bacterial strains whose genome sequences and the ORF information are available in the GenBank database. We carried out BLAST search using RakEF sequence of Micromonospora sp. DSW705 and Streptomyces sp. MWW064 as the queries, and then analyzed each of the gene clusters encoding RakEF orthologues using antiSMASH  and manually if necessary. As shown in Fig. 4, three Micromonospora , 19 Streptomyces , three Frankia , one Nocardiopisis, one Salinispora , and two Kitasatospora strains were found to possess hybrid PKS/NRPS gene clusters encoding RakEF orthologues. On the basis of the domain organizations and amino-acids substrates of A domains, these gene clusters can be classified into four groups (Fig. 4).
M. purpureochromogenes NRRL B-2672 harbors a rak cluster as same as Micromonospora sp. DSW705 and Streptomyces sp. MWW064. Micromonospora sp. M42 also possesses almost the same cluster, but the methyltransferase (MT) domain in module 5 (m5) is not present and some ORFs are fragmented (Fig. 4a).
Eighteen gene clusters categorized into Fig. 4b have domain organizations similar to rak clusters but the substrate of A domain in m6 was predicted to be L-valine. As vinylamycin and microtermolide contain a valine residue in their depsipeptide structure [1, 2], the four gene clusters of “ Streptomyces rubellomurinus” ATCC 31215 and three Frankia strains were proposed to be responsible for vinylamycin biosynthesis. A plausible biosynthetic pathway for vinylamycin is illustrated in Fig. 5a. If the loading modules incorporate a C3 unit or LMs encode an AT domain for a C3 starter instead of the CoA-ligase domain, the cluster is likely responsible for microtermolide biosynthesis. The remaining 14 strains in Fig. 4b lack a KR domain in m2. In the clusters of eight among the 18 strains, NRPSs for m5 and m6 are encoded the complementary strands, although the cluster of Streptomyces durhamensis NRRL ISP-5539T was not completely sequenced. Streptomyces sp. 769 does not have the PKS for LM and m1. In the cluster of Streptomyces sp. MspMP-M5, the PKS likely for LM and m1 is encoded downstream of the PKS gene for m4, although the gene cluster was not completely sequenced. The cluster of Nocardiposis sp. CNS639 likely lacks a LM, and some domains are distinct from those of other strains.
Gene clusters of Salinispora arenicola CNR107 and Micromonospora sp. RV43 contain three NRPS modules at m3, m4, and m6, which were predicted to incorporate glycine, serine, and glycine, respectively. Only BE-43547 is known as a depsipeptide containing two glycines and APDA moiety. According to the domain organization, these two clusters are proposed to be involved with BE-43547 production as illustrated in Fig. 5b.
Figure 4d shows gene clusters in which the last NRPS module incorporates amino acids different from those of the other three groups described above. Five gene clusters shown in green were predicted to incorporate L-tyrosine into the polyketide/nonribosomal peptide chains by m6. Since depsipeptides bearing both tyrosine and APDA residues are not known, products from these clusters may be structurally novel. Two gene clusters of Streptomyces celluloflavas NRRL B-2493T and Streptomyces albus subsp. albus NRRL B-2513 showed the same domain organization as rak clusters, but NRPS substrate prediction suggests incorporation of L-glutamate and L-tryptophan/β-hydroxy-tyrosine (bht) by m6, respectively. Because rakicidin analogues containing these amino acids in place of the asparagine residue have not been reported, production of novel APDA-containing peptides is expected in these strains.
Distribution of the gene clusters among genome-sequenced strains
Whole genome sequencing has been performed for a large number of actinomycete strains. At present, genome sequences of over 227 Streptomyces species, eight species and six strains of Kitasatospora , eight species and seven strains of Micromonospora , three Salinispora species, one species and 97 strains of Frankia , and 18 species and 6 strains of Nocardiopsis are available from the GenBank database. Among them, 29 strains possess the rak-like gene clusters. To investigate the correlation between evolution and secondary metabolite gene distribution, strains harboring the rak-like gene clusters (shaded in black) were mapped onto the phylogenetic tree of genome-sequenced strains based on 16S rRNA gene sequences (Fig. 6). Micromonospora strains are divided into two clades, one of which includes three rakicidin-producers and one BE-43547-producer. Strain MWW064 is the only Streptomyces that possesses the rak cluster other than Micromonospora . In contrast, vinylamycin-related gene clusters, shown in blue, are distributed in taxonomically diverse Streptomyces strains. It is noteworthy that two Frankia strains have the same gene cluster whereas only four compounds have been described for Frankia species . This genus should be more examined for secondary metabolite production. BE-43547 gene clusters are present only in two strains of two genera belonging to the family Micromonosporaceae in this analysis. But, since this compound was originally found from Streptomyces , the gene cluster must also be present in the genus Streptomyces . Presence of gene clusters for depsipeptides containing a tyrosine residue is limited to the genus Kitasatospora and phylogenetically close Streptomyces members. The S. celluloflavas NRRL B-2493T gene cluster shows a similar domain organization to those of rak clusters stated above, but this strain is not taxonomically close to rakicidin producers.
The 6.8 Mb draft genome of Micromonospora sp. DSW705, a producer of rakicidins A and B isolated from deep seawater, has been deposited at GenBank/ENA/DDBJ under the accession number BBVA00000000. This strain contains seven PKS and NRPS gene clusters, from which rakicidin-biosynthetic gene cluster was identified. Gene clusters for the synthesis of rakicidins or the related compounds are present in taxonomically diverse actinomycete strains, belonging to Micromonospora , Salinispora , Frankia , Nocardiposis, Kitasatospora , and Streptomyces . These findings provide useful information for discovering new and diverse depsipeptides bearing the APDA unit, and accelerate understanding of relationship between taxonomy and secondary metabolite gene distribution, and will possibly provide the insight regarding to the evolution of secondary metabolite genes.
Acyl carrier protein
DNA Data Bank of Japan
International Streptomyces project
Biological Resource Center, National Institute of Technology and Evaluation
Nonribosomal peptide synthetase
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This research was supported by a Grant-in-aid for Scientific Research from the Ministry of Education, Culture, Sports, and Technology of Japan to Y.I. We also thank Dr. Akane Kimura, Ms. Yuko Kitahashi, Ms. Satomi Saitou and Ms. Chiyo Shibata for assistance to this study.
HK analysed biosynthetic gene clusters and drafted the manuscript. NI annotated the genome sequences. AH sequenced the genome. MH performed chemotaxonomic experiments. EH examined the features of the strain. AI predicted products of gene clusters similar to rak clusters. YI designed this study and edited the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing of interests.
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Komaki, H., Ichikawa, N., Hosoyama, A. et al. Draft genome sequence of Micromonospora sp. DSW705 and distribution of biosynthetic gene clusters for depsipeptides bearing 4-amino-2,4-pentadienoate in actinomycetes. Stand in Genomic Sci 11, 84 (2016) doi:10.1186/s40793-016-0206-2
- Nonribosomal peptide synthetase
- Polyketide synthase