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Abstract

A Gram-stain-negative bacterium, designated IO390501, was isolated from a sea water sample from the Indian Ocean and taxonomically characterized using a polyphasic approach. The strain is phylogenetically close to '' L15 and IPL18, with 16S rRNA gene sequence similarity of 97.7 and 97.4 %, respectively. The genome of IO390501 has a DNA G+C content of 61.9 mol% for the 3.9 Mb chromosome. Genome-based phylogenetic trees indicated that IO390501 clusters as an independent lineage with '' L15. Genomic relatedness of DNA–DNA hybridization between IO390501 and phylogenetic neighbours ranged from 18.8 to 21.5 %, below the cutoff of 70 %, and corresponding average nucleotide identity values were between 71.4 and 79.0 %, lower than the 95.0 % threshold. The predominant cellular fatty acids of IO390501 are summed feature 8 (Cω7/ ω6) and C. IO390501 contains ubiquinone-10 as the sole respiratory quinone, and phosphatidylglycerol and glycolipids as the major polar lipids. On the basis of the results of phenotypic, chemotaxonomic and genetic analyses, strain IO390501 represents a novel species of the genus for which the name sp. nov. is proposed. The type strain is IO390501.

Funding
This study was supported by the:
  • the China Ocean Mineral Resources R and D Association (CPMRA) (Award DY135-E2-02-07)
    • Principle Award Recipient: Jifang Yang
  • the Zhejiang Provincial Top Key Discipline of Biological Engineering (Award CX2018006, CX2018007, CX2018019)
    • Principle Award Recipient: Jigang Chen
  • the Ningbo Public Service Platform for High-Value Utilization of Marine Biological Resources (Award NBHY-2017-P2)
    • Principle Award Recipient: Jigang Chen
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2020-02-03
2024-04-25
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References

  1. Nakagawa Y, Sakane T, Yokota A. Transfer of "Pseudomonas riboflavina" (Foster 1944), a Gram-negative, motile rod with long-chain 3-hydroxy fatty acids, to Devosia riboflavina gen. nov., sp. nov., nom. rev. Int J Syst Bacteriol 1996; 46:16–22 [View Article]
    [Google Scholar]
  2. Yoon J-H, Kang S-J, Park S, Oh T-K. Devosia insulae sp. nov., isolated from soil, and emended description of the genus Devosia . Int J Syst Evol Microbiol 2007; 57:1310–1314 [View Article]
    [Google Scholar]
  3. Parte AC. LPSN - List of prokaryotic names with standing in nomenclature (bacterio.net), 20 years on. Int J Syst Evol Microbiol 2018; 68:1825–1829 [View Article]
    [Google Scholar]
  4. Mohd Nor MN, Sabaratnam V, Tan GYA. Devosia elaeis sp. nov., isolated from oil palm rhizospheric soil. Int J Syst Evol Microbiol 2017; 67:851–855 [View Article]
    [Google Scholar]
  5. Vanparys B, Heylen K, Lebbe L, De Vos P. Devosia limi sp. nov., isolated from a nitrifying inoculum. Int J Syst Evol Microbiol 2005; 55:1997–2000 [View Article]
    [Google Scholar]
  6. Xu L, Zhang Y, Read N, Liu S, Friman V-P. Devosia nitraria sp. nov., a novel species isolated from the roots of Nitraria sibirica in China. Antonie van Leeuwenhoek 2017; 110:1475–1483 [View Article]
    [Google Scholar]
  7. Lane DJ. 16S/23S rRNA sequencing. In Stackebrandt E, Goodfellow M. (editors) Nucleic A cid Techniques in Bacterial Systematics Chichester, UK: John Wiley & Sons; 1991 pp 115–175
    [Google Scholar]
  8. Kumar S, Stecher G, Tamura K. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol 2016; 33:1870–1874 [View Article]
    [Google Scholar]
  9. Kimura M. A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J Mol Evol 1980; 16:111–120 [View Article]
    [Google Scholar]
  10. Na S-I, Kim YO, Yoon S-H, Ha S-M, Baek I et al. UBCG: up-to-date bacterial core gene set and pipeline for phylogenomic tree reconstruction. J Microbiol 2018; 56:280–285 [View Article]
    [Google Scholar]
  11. Zuo G, Hao B. CVTree3 web server for whole-genome-based and alignment-free prokaryotic phylogeny and taxonomy. Genomics Proteomics Bioinformatics 2015; 13:321–331 [View Article]
    [Google Scholar]
  12. Seemann T. Prokka: rapid prokaryotic genome annotation. Bioinformatics 2014; 30:2068–2069 [View Article]
    [Google Scholar]
  13. Nordberg H, Cantor M, Dusheyko S, Hua S, Poliakov A et al. The genome portal of the Department of Energy Joint Genome Institute: 2014 updates. Nucleic Acids Res 2014; 42:D26–D31 [View Article]
    [Google Scholar]
  14. Yoon S-H, Ha S-M, Lim J, Kwon S, Chun J. A large-scale evaluation of algorithms to calculate average nucleotide identity. Antonie van Leeuwenhoek 2017; 110:1281–1286 [View Article]
    [Google Scholar]
  15. Meier-Kolthoff JP, Auch AF, Klenk H-P, Göker M. Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinformatics 2013; 14:60 [View Article]
    [Google Scholar]
  16. Colston SM, Fullmer MS, Beka L, Lamy B, Gogarten JP et al. Bioinformatic genome comparisons for taxonomic and phylogenetic assignments using Aeromonas as a test case. MBio 2014; 5:e02136–14 [View Article]
    [Google Scholar]
  17. Chun J, Oren A, Ventosa A, Christensen H, Arahal DR 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 [View Article]
    [Google Scholar]
  18. Lai Q, Cao J, Yuan J, Li F, Shao Z. Celeribacter indicus sp. nov., a polycyclic aromatic hydrocarbon-degrading bacterium from deep-sea sediment and reclassification of Huaishuia halophila as Celeribacter halophilus comb. nov. Int J Syst Evol Microbiol 2014; 64:4160–4167 [View Article]
    [Google Scholar]
  19. Smibert RM, Krieg NR. Phenotypic characterization. In Gerhardt P, Murray RGE. (editors) Methods for General and Molecular Bacteriology Washington, DC: Wood WA, Krieg NR; 1994 pp 607–654
    [Google Scholar]
  20. Komagata K, Suzuki K. Lipid and cell-wall analysis in bacterial systematics. Methods Microbiol 1987; 19:161–207
    [Google Scholar]
  21. da Costa MS, Albuquerque L, Nobre MF, Wait R. The identification of polar lipids in prokaryotes. Methods Microbiol 2011; 38:165–181
    [Google Scholar]
  22. Dua A, Malhotra J, Saxena A, Khan F, Lal R. Devosia lucknowensis sp. nov., a bacterium isolated from hexachlorocyclohexane (HCH) contaminated pond soil. J Microbiol 2013; 51:689–694 [View Article]
    [Google Scholar]
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