1887

Abstract

A novel bacterial strain, A3, was isolated from the intestines of the sea urchin collected in Øresund, Denmark. The strain was Gram-reaction-negative, rod-shaped and facultatively anaerobic, and displayed growth at 5–25 °C (optimum 20 °C), pH 7–9 (optimum at pH 7) and 1–6 % (w/v) NaCl (optimum 3 %). Furthermore, strain A3 grew on agar, agarose, -carrageenan, alginate and laminarin as sole carbon source. Complete liquefaction of agar and -carrageenan was observed on solid plate media as a result of enzymatic activities. Major fatty acids were summed feature 3 (Cω7 and/or Cω6) and C. The respiratory quinones were determined to be ubiquinones Q-8 (92 %) and Q-7 (8 %), and polar lipids were phosphatidylethanolamine, phosphatidylglycerol and diphosphatidylglycerol. The DNA G+C content was 36.9 mol%. Phylogenetical analyses based on the 16S rRNA gene showed that the bacterium was affiliated with the genus within the of the . The level of 16S rRNA gene sequence similarity between strain A3 and its closest relatives in the genus ( ATCC 27364 and KMD 002) was 97.5 %. The average nucleotide identity between strain A3 and other members of was 78.6–80.5 %, and DNA–DNA hybridization prediction revealed values of less than 23 % relatedness between strain A3 and other species. The phenotypic, phylogenetic and genomic analyses support the hypothesis that strain A3 represents a novel species of the genus , for which the name sp. nov. is proposed. The type strain is A3 (=LMG 30125=NCIMB 15095).

Loading

Article metrics loading...

/content/journal/ijsem/10.1099/ijsem.0.002568
2018-02-01
2024-04-20
Loading full text...

Full text loading...

/deliver/fulltext/ijsem/68/2/687.html?itemId=/content/journal/ijsem/10.1099/ijsem.0.002568&mimeType=html&fmt=ahah

References

  1. Deming JW, Somers LK, Straube WL, Swartz DG, Macdonell MT. Isolation of an obligately barophilic bacterium and description of a new genus, Colwellia gen. nov. Syst Appl Microbiol 1988; 10:152–160 [View Article]
    [Google Scholar]
  2. Bowman JP, Gosink JJ, Mccammon SA, Lewis TE, Nichols DS et al. Colwellia demingiae sp. nov., Colwellia hornerae sp. nov., Colwellia rossensis sp. nov. and Colwellia psychrotropica sp. nov.: psychrophilic Antarctic species with the ability to synthesize docosahexaenoic acid (22:ω63). Int J Syst Bacteriol 1998; 48:1171–1180 [View Article]
    [Google Scholar]
  3. Kim YO, Park IS, Park S, Nam BH, Jung YT et al. Colwellia mytili sp. nov., isolated from mussel Mytilus edulis. Int J Syst Evol Microbiol 2017; 67:31–36 [View Article][PubMed]
    [Google Scholar]
  4. Kusube M, Kyaw TS, Tanikawa K, Chastain RA, Hardy KM et al. Colwellia marinimaniae sp. nov., a hyperpiezophilic species isolated from an amphipod within the Challenger Deep, Mariana Trench. Int J Syst Evol Microbiol 2017; 67:824–831 [View Article][PubMed]
    [Google Scholar]
  5. Choi EJ, Kwon HC, Koh HY, Kim YS, Yang HO. Colwellia asteriadis sp. nov., a marine bacterium isolated from the starfish Asterias amurensis. Int J Syst Evol Microbiol 2010; 60:1952–1957 [View Article][PubMed]
    [Google Scholar]
  6. Yumoto I, Kawasaki K, Iwata H, Matsuyama H, Okuyama H. Assignment of Vibrio sp. strain ABE-1 to Colwellia maris sp. nov., a new psychrophilic bacterium. Int J Syst Bacteriol 1998; 48:1357–1362 [View Article][PubMed]
    [Google Scholar]
  7. Nogi Y, Hosoya S, Kato C, Horikoshi K. Colwellia piezophila sp. nov., a novel piezophilic species from deep-sea sediments of the Japan Trench. Int J Syst Evol Microbiol 2004; 54:1627–1631 [View Article][PubMed]
    [Google Scholar]
  8. Jung SY, Oh TK, Yoon JH. Colwellia aestuarii sp. nov., isolated from a tidal flat sediment in Korea. Int J Syst Evol Microbiol 2006; 56:33–37 [View Article][PubMed]
    [Google Scholar]
  9. Xu ZX, Zhang HX, Han JR, Dunlap CA, Rooney AP et al. Colwellia agarivorans sp. nov., an agar-digesting marine bacterium isolated from coastal seawater. Int J Syst Evol Microbiol 2017; 67:1969–1974 [View Article][PubMed]
    [Google Scholar]
  10. Liu Y, Liu LZ, Zhong ZP, Zhou YG, Liu Y et al. Colwellia aquaemaris sp. nov., isolated from the Cynoglossus semilaevis culture tank in a recirculating mariculture system. Int J Syst Evol Microbiol 2014; 64:3926–3930 [View Article][PubMed]
    [Google Scholar]
  11. Wang FQ, Lin XZ, Chen GJ, Du ZJ. Colwellia arctica sp. nov., isolated from Arctic marine sediment. Antonie van Leeuwenhoek 2015; 107:723–729 [View Article][PubMed]
    [Google Scholar]
  12. Yu Y, Li HR, Zeng YX. Colwellia chukchiensis sp. nov., a psychrotolerant bacterium isolated from the Arctic Ocean. Int J Syst Evol Microbiol 2011; 61:850–853 [View Article][PubMed]
    [Google Scholar]
  13. Kim YO, Park S, Nam BH, Jung YT, Kim DG et al. Colwellia meonggei sp. nov., a novel gammaproteobacterium isolated from sea squirt Halocynthia roretzi. Antonie van Leeuwenhoek 2013; 104:1021–1027 [View Article][PubMed]
    [Google Scholar]
  14. Zhang DC, Yu Y, Xin YH, Liu HC, Zhou PJ et al. Colwellia polaris sp. nov., a psychrotolerant bacterium isolated from Arctic sea ice. Int J Syst Evol Microbiol 2008; 58:1931–1934 [View Article][PubMed]
    [Google Scholar]
  15. Park S, Jung YT, Yoon JH. Colwellia sediminilitoris sp. nov., isolated from a tidal flat. Int J Syst Evol Microbiol 2016; 66:3258–3263 [View Article][PubMed]
    [Google Scholar]
  16. Martin M, Barbeyron T, Martin R, Portetelle D, Michel G et al. The cultivable surface microbiota of the brown alga Ascophyllum nodosum is enriched in macroalgal-polysaccharide-degrading bacteria. Front Microbiol 2015; 6:1487 [View Article][PubMed]
    [Google Scholar]
  17. Romanenko LA, Zhukova NV, Rohde M, Lysenko AM, Mikhailov VV et al. Glaciecola mesophila sp. nov., a novel marine agar-digesting bacterium. Int J Syst Evol Microbiol 2003; 53:647–651 [View Article][PubMed]
    [Google Scholar]
  18. Powers EM. Efficacy of the Ryu nonstaining KOH technique for rapidly determining gram reactions of food-borne and waterborne bacteria and yeasts. Appl Environ Microbiol 1995; 61:3756–3758[PubMed]
    [Google Scholar]
  19. Thomas F, Barbeyron T, Michel G. Evaluation of reference genes for real-time quantitative PCR in the marine flavobacterium Zobellia galactanivorans. J Microbiol Methods 2011; 84:61–66 [View Article][PubMed]
    [Google Scholar]
  20. Miller LT. A single derivatization method for bacterial fatty acid methyl esters including hydroxy acids. J Clin Microbiol 1982; 16:584–586
    [Google Scholar]
  21. Kuykendall LD, Roy MA, O'Neill JJ, Devine TE. Fatty acids, antibiotic resistance, and deoxyribonucleic acid homology groups of Bradyrhizobium japonicum. Int J Syst Bacteriol 1988; 38:358–361 [View Article]
    [Google Scholar]
  22. Tindall BJ, Sikorski J, Smibert RM, Kreig NR. Phenotypic characterization and the principles of comparative systematics. In Reddy CA, Beveridge TJ, Breznak JA, Marzluf G, Schmidt TM et al. (editors) Methods for General and Molecular Microbiology, 3rd ed. Washington, DC, USA: ASM Press; pp. 330–393
    [Google Scholar]
  23. Schultz-Johansen M, Glaring MA, Bech PK, Stougaard P. Draft genome sequence of a novel marine bacterium, Paraglaciecola sp. strain S66, with hydrolytic activity against seaweed polysaccharides. Genome Announc 2016; 4:e00304-16 [View Article][PubMed]
    [Google Scholar]
  24. Katoh K, Misawa K, Kuma K, Miyata T. MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform. Nucleic Acids Res 2002; 30:3059–3066 [View Article][PubMed]
    [Google Scholar]
  25. Tamura K, Peterson D, Peterson N, Stecher G, Nei M et al. MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 2011; 28:2731–2739 [View Article][PubMed]
    [Google Scholar]
  26. Meier-Kolthoff JP, Auch AF, Klenk HP, Göker M. Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinformatics 2013; 14:60 [View Article][PubMed]
    [Google Scholar]
  27. Meier-Kolthoff JP, Göker M, Spröer C, Klenk HP. When should a DDH experiment be mandatory in microbial taxonomy?. Arch Microbiol 2013; 195:413–418 [View Article][PubMed]
    [Google Scholar]
  28. Goris J, Konstantinidis KT, Klappenbach JA, Coenye T, Vandamme P et al. DNA–DNA hybridization values and their relationship to whole-genome sequence similarities. Int J Syst Evol Microbiol 2007; 57:81–91 [View Article][PubMed]
    [Google Scholar]
  29. Richter M, Rosselló-Móra R. Shifting the genomic gold standard for the prokaryotic species definition. Proc Natl Acad Sci USA 2009; 106:19126–19131 [View Article][PubMed]
    [Google Scholar]
  30. Auch AF, Klenk HP, Göker M. Standard operating procedure for calculating genome-to-genome distances based on high-scoring segment pairs. Stand Genomic Sci 2010; 2:142–148 [View Article][PubMed]
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/ijsem/10.1099/ijsem.0.002568
Loading
/content/journal/ijsem/10.1099/ijsem.0.002568
Loading

Data & Media loading...

Supplements

Supplementary File 1

PDF
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error