Abstract
Here, we report the draft genome sequence of Thermogemmatispora onikobensis NBRC 111776T, an aerial mycelium- and spore-forming thermophilic bacterium belonging to the class Ktedonobacteria. The genome contains five biosynthetic gene clusters coding for secondary metabolites, such as terpene, thiopeptide, lantipeptide, nonribosomal peptide, and lassopeptide, suggesting the potential to produce secondary metabolites.
GENOME ANNOUNCEMENT
Thermogemmatispora onikobensis ONI-1T, isolated from fallen leaves on geothermal soils, is a thermophilic, Gram-positive, and sporulating bacterium belonging to the class Ktedonobacteria within the phylum Chloroflexi (1). The class Ktedonobacteria contains six cultured species with validly published names: Ktedonobacter racemifer (2), Thermosporothrix hazakensis (3), Thermogemmatispora onikobensis, Thermogemmatispora foliorum (1), Thermogemmatispora carboxidivorans (4), and Thermosporothrix narukonensis (5). The complete genome sequence of Ktedonobacter racemifer SOSP1-21T has already been reported (6). Since these species form branched vegetative and aerial mycelia, their colony morphologies resemble those of actinomycetes of the phylum Actinobacteria. Actinomycetes are widely recognized as rich sources for a variety of bioactive secondary metabolites (7), and secondary metabolism is often associated with morphological developments in microorganisms (8–10). Therefore, members of the class Ktedonobacteria are recently expected as new sources, and indeed, new compounds were discovered from T. hazakensis SK20-1T (11). The genome project for T. hazakensis SK20-1T is also ongoing (12, 13), which suggests that the genome contains many biosynthetic gene clusters coding for secondary metabolites, such as polyketides and nonribosomal peptides (13). In contrast, the diversity of secondary metabolic pathways in the genus Thermogemmatispora was unclear, because no genome information of this genus had been available when we began this study. Hence, we conducted genome sequencing of T. onikobensis to assess its potential as a secondary metabolite producer.
T. onikobensis ONI-1T was deposited into the NBRC culture collection and has been registered as NBRC 111776T. The whole genome of T. onikobensis NBRC 111776T was sequenced by paired-end sequencing with MiSeq (Illumina; 792-Mb sequences, 142.5-fold coverage). These reads were assembled using Newbler version 3.0 and subsequently finished using GenoFinisher (14), which led to a final assembly of 112 scaffold sequences of >500 bp each. The total size of the assembly was 5,556,501 bp, with a G+C content of 61.1%. Secondary metabolic gene clusters were surveyed using antiSMASH (15). The genome harbors biosynthetic gene clusters for terpene, thiopeptide-lantipeptide, lantipeptide, and lassopeptide, which are encoded in scaffold00005, scaffold00006, scaffold00015, and scaffold00090, respectively. A biosynthetic gene cluster for nonribosomal peptide is also present, but it was not completely sequenced and is divided into scaffold00050, scaffold00083, and scaffold00122.
During this study, the draft genome sequence of Thermogemmatispora carboxidivorans PM5T (GenBank accession no. JNIM01000001) was released to the public. The genome of T. carboxidivorans PM5T also possesses biosynthetic gene clusters for terpene, thiopeptide-lantipeptide, lantipeptide, and nonribosomal peptide, which are similar to those of T. onikobensis ONI-1T, suggesting that these four clusters are conserved in the genus Thermogemmatispora. In contrast, the lassopeptide biosynthetic gene cluster is specific to T. onikobensis ONI-1T, since T. carboxidivorans PM5T does not harbor any lassopeptide biosynthetic gene clusters.
Here, we publish the draft genome sequence of T. onikobensis ONI-1T. The genome sequence will provide significant information to elucidate the potential as a secondary metabolite producer.
Accession number(s).
The draft genome sequence of Thermogemmatispora onikobensis NBRC 111776T has been deposited in the DDBJ/ENA/GenBank database under the accession no. BDGT00000000. The version described in this paper is the first version, BDGT01000000.
ACKNOWLEDGMENTS
This work was supported by the Ministry of Economy, Trade and Industry of Japan.
We thank Keiko Tsuchikane and Yuko Kitahashi for genome sequencing and finishing the genome sequence, respectively.
Footnotes
Citation Komaki H, Hosoyama A, Yabe S, Yokota A, Uchino Y, Takano H. 2016. Draft genome sequence of Thermogemmatispora onikobensis NBRC 111776T, an aerial mycelium- and spore-forming thermophilic bacterium belonging to the class Ktedonobacteria. Genome Announc 4(5):e01156-16. doi:10.1128/genomeA.01156-16.
REFERENCES
- 1.Yabe S, Aiba Y, Sakai Y, Hazaka M, Yokota A. 2011. Thermogemmatispora onikobensis gen. nov., sp. nov. and Thermogemmatispora foliorum sp. nov., isolated from fallen leaves on geothermal soils, and description of Thermogemmatisporaceae fam. nov. and Thermogemmatisporales ord. nov. within the class Ktedonobacteria. Int J Syst Evol Microbiol 61:903–910. doi: 10.1099/ijs.0.024877-0. [DOI] [PubMed] [Google Scholar]
- 2.Cavaletti L, Monciardini P, Bamonte R, Schumann P, Rohde M, Sosio M, Donadio S. 2006. New lineage of filamentous, spore-forming, Gram-positive bacteria from soil. Appl Environ Microbiol 72:4360–4369. doi: 10.1128/AEM.00132-06. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Yabe S, Aiba Y, Sakai Y, Hazaka M, Yokota A. 2010. Thermosporothrix hazakensis gen. nov., sp. nov., isolated from compost, description of Thermosporotrichaceae fam. nov. within the class Ktedonobacteria Cavaletti et al. 2007 and emended description of the class Ktedonobacteria. Int J Syst Evol Microbiol 60:1794–1801. doi: 10.1099/ijs.0.018069-0. [DOI] [PubMed] [Google Scholar]
- 4.King CE, King GM. 2014. Description of Thermogemmatispora carboxidivorans sp. nov., a carbon-monoxide-oxidizing member of the class Ktedonobacteria isolated from a geothermally heated biofilm, and analysis of carbon monoxide oxidation by members of the class Ktedonobacteria. Int J Syst Evol Microbiol 64:1244–1251. doi: 10.1099/ijs.0.059675-0. [DOI] [PubMed] [Google Scholar]
- 5.Yabe S, Sakai Y, Yokota A. 2016. Thermosporothrix narukonensis sp. nov., belonging to the class Ktedonobacteria, isolated from fallen leaves on geothermal soil, and emended description of the genus Thermosporothrix. Int J Syst Evol Microbiol 66:2152–2157. doi: 10.1099/ijsem.0.001004. [DOI] [PubMed] [Google Scholar]
- 6.Chang YJ, Land M, Hauser L, Chertkov O, Del Rio TG, Nolan M, Copeland A, Tice H, Cheng JF, Lucas S, Han C, Goodwin L, Pitluck S, Ivanova N, Ovchinikova G, Pati A, Chen A, Palaniappan K, Mavromatis K, Liolios K, Brettin T, Fiebig A, Rohde M, Abt B, Goker M, Detter JC, Woyke T, Bristow J, Eisen JA, Markowitz V, Hugenholtz P, Kyrpides NC, Klenk HP, Lapidus A. 2011. Non-contiguous finished genome sequence and contextual data of the filamentous soil bacterium Ktedonobacter racemifer type strain (SOSP1-21). Stand Genomic Sci 5:97–111. doi: 10.4056/sigs.2114901. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Bérdy J. 2005. Bioactive microbial metabolites. J Antibiot (Tokyo) 58:1–26. doi: 10.1038/ja.2005.1. [DOI] [PubMed] [Google Scholar]
- 8.Flärdh K, Buttner MJ. 2009. Streptomyces morphogenetics: dissecting differentiation in a filamentous bacterium. Nat Rev Microbiol 7:36–49. doi: 10.1038/nrmicro1968. [DOI] [PubMed] [Google Scholar]
- 9.Horinouchi S, Beppu T. 2007. Hormonal control by A-factor of morphological development and secondary metabolism in Streptomyces. Proc Jpn Acad Ser B Phys Biol Sci 83:277–295. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Wenzel SC, Müller R. 2009. Myxobacteria—“microbial factories” for the production of bioactive secondary metabolites. Mol Biosyst 5:567–574. doi: 10.1039/b901287g. [DOI] [PubMed] [Google Scholar]
- 11.Park J, Yabe S, Shin-ya K, Nishiyama M, Kuzuyama T. 2015. New 2-(1′H-indole-3′-carbonyl)-thiazoles derived from the thermophilic bacterium Thermosporothrix hazakensis SK20-1T. J Antibiot (Tokyo) 68:60–62. doi: 10.1038/ja.2014.93. [DOI] [PubMed] [Google Scholar]
- 12.Park JS, Kagaya N, Hashimoto J, Izumikawa M, Yabe S, Shin-Ya K, Nishiyama M, Kuzuyama T. 2014. Identification and biosynthesis of new acyloins from the thermophilic bacterium Thermosporothrix hazakensis SK20-1(T). Chembiochem 15:527–532. doi: 10.1002/cbic.201300690. [DOI] [PubMed] [Google Scholar]
- 13.Yabe S. 2012. Isolation, systematic classification and genome analysis of novel thermophilic bacteria─characteristic of actinomycetes-like bacteria belonging to the class Ktedonobacteira within the phylum Chloroflexi. Microbiol Cult Collect 28:109–120. http://www.jsmrs.jp/journal/No28_2/No28_2_109.pdf. [Google Scholar]
- 14.Ohtsubo Y, Maruyama F, Mitsui H, Nagata Y, Tsuda M. 2012. Complete genome sequence of Acidovorax sp. strain KKS102, a polychlorinated-biphenyl degrader. J Bacteriol 194:6970–6971. doi: 10.1128/JB.01848-12. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Weber T, Blin K, Duddela S, Krug D, Kim HU, Bruccoleri R, Lee SY, Fischbach MA, Müller R, Wohlleben W, Breitling R, Takano E, Medema MH. 2015. antiSMASH 3.0–a comprehensive resource for the genome mining of biosynthetic gene clusters. Nucleic Acids Res 43:W237–W243. doi: 10.1093/nar/gkv437. [DOI] [PMC free article] [PubMed] [Google Scholar]
