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Abstract

Two Gram-staining-negative, aerobic, rod-shaped bacteria NNCM1 and NNCM2 were isolated from the scleractinian coral . NNCM1 grew with 0.5–12 % (w/v) NaCl (optimum, 3–6 %), at 18–37 °C (optimum, 28 °C) and at pH 6.0–10.0 (optimum, 7.0–8.0). NNCM2 grew with 0.5–10 % (w/v) NaCl (optimum, 2 %), at 18–37 °C (optimum, 28 °C) and at pH 6.5–9.0 (optimum, 7.0). The results of phylogenetic analysis based on 16S rRNA gene sequences indicated that NNCM1 formed a lineage within the genus of the family Algiphilaceae, and it was distinct from the most closely related species DG1253, with a 16S rRNA gene sequences similarity of 97.05 %. NNCM2 formed a lineage within the family Rhodobacteraceae, and it was distinct from the closely related genera CAU 1123, D4M1 and MME-001 with 93.41, 92.78 and 91.09% identities, respectively. The major respiratory quinone was Q-8 and Q-10 for NNCM1 and NNCM2, respectively. The predominant fatty acids (more than 10 %) were summed feature 8 (39.4 %) and C (19.4 %) for NNCM1 and summed feature 8 (62.8 %) and C (12.4 %) for NNCM2. The DNA G+C contents of NNCM1 and NNCM2 were 63.3 and 63.4 mol% respectively. The polar lipids of NNCM1 comprised one diphosphatidylglycerol, one phosphatidylethanolamine, one phosphatidylglycerol and one unknown polar lipid, while those of NNCM2 comprised one phosphatidylethanolamine, one phosphatidylglycerol, one aminolipid and four unknown polar lipids. Phenotypic characteristics (physiological, biochemical and chemotaxonomic) also supported the taxonomic novelty of the two isolates. Thus, NNCM1 is considered to represent a novel species within genus , for which the name sp. nov. is proposed. The type strain is NNCM1 (=KCTC 82966=MCCC 1K06445). NNCM2 represents a novel genus and species within the family Rhodobacteraceae, for which the name gen. nov. sp. nov. is proposed. The type strain is NNCM2 (=KCTC 82967=MCCC 1K06408).

Funding
This study was supported by the:
  • Guangdong Key Area R & D Program Project (Award 2020B1111030002)
    • Principle Award Recipient: BaohuaXiao
  • Shenzhen Science and Technology R&D Fund (Award JCYJ20200109144803833)
    • Principle Award Recipient: BaohuaXiao
  • Shenzhen Science and Technology R&D Fund (Award KJYY20180213182720347)
    • Principle Award Recipient: BaohuaXiao
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2022-04-19
2024-04-20
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References

  1. Gutierrez T, Green DH, Whitman WB, Nichols PD, Semple KT et al. Algiphilus aromaticivorans gen. nov., sp. nov., an aromatic hydrocarbon-degrading bacterium isolated from a culture of the marine dinoflagellate Lingulodinium polyedrum, and proposal of Algiphilaceae fam. nov. Int J Syst Evol Microbiol 2012; 62:2743–2749 [View Article] [PubMed]
    [Google Scholar]
  2. Famintzin A. Eine neue bacterienform: Nevskia ramosa. Bulletin of the Academy of Science St Petersbourg 1892; New series 2 volume 34:481–486
    [Google Scholar]
  3. Sneath PHA, McGowan V, Skerman VBD. Approved lists of bacterial names. Int J Syst Evol Microbiol 1980; 30:225–420 [View Article]
    [Google Scholar]
  4. Elifantz H, Horn G, Ayon M, Cohen Y, Minz D. Rhodobacteraceae are the key members of the microbial community of the initial biofilm formed in Eastern Mediterranean coastal seawater. FEMS Microbiol Ecol 2013; 85:348–357 [View Article] [PubMed]
    [Google Scholar]
  5. Shin YH, Kim J-H, Suckhoom A, Kantachote D, Kim W. Limibaculum halophilum gen. nov., sp. nov., a new member of the family Rhodobacteraceae. Int J Syst Evol Microbiol 2017; 67:3812–3818 [View Article]
    [Google Scholar]
  6. Liu P, Ding W, Lai Q, Liu R, Wei Y et al. Physiological and genomic features of Paraoceanicella profunda gen. nov., sp. nov., a novel piezophile isolated from deep seawater of the Mariana Trench. Microbiologyopen 2020; 9:e966 [View Article]
    [Google Scholar]
  7. Cha I-T, Park I, Lee H-W, Lee H, Park J-M et al. Pseudoruegeria aestuarii sp. nov., of the family Rhodobacteraceae, isolated from a tidal flat. Int J Syst Evol Microbiol 2016; 66:3125–3131 [View Article] [PubMed]
    [Google Scholar]
  8. Imhoff JF, Truper HG, Pfennig N. Rearrangement of the species and genera of the pSpecies and Genera of the Phototrophic “Purple Nonsulfur Bacteria.”. Int J Syst Bacteriol 1984; 34:340–343 [View Article]
    [Google Scholar]
  9. Zhou JL, Maskaoui K. Distribution of polycyclic aromatic hydrocarbons in water and surface sediments from Daya Bay, China. Environ Pollut 2003; 121:269–281 [View Article] [PubMed]
    [Google Scholar]
  10. Wang YS, Lou ZP, Sun CC, Sun S. Ecological environment changes in Daya Bay, China, from 1982 to 2004. Mar Pollut Bull 2008; 56:1871–1879 [View Article] [PubMed]
    [Google Scholar]
  11. Zhang L, Xiong L, Li J, Huang X. Long-term changes of nutrients and biocenoses indicating the anthropogenic influences on ecosystem in Jiaozhou Bay and Daya Bay, China. Mar Pollut Bull 2021; 168:112406 [View Article] [PubMed]
    [Google Scholar]
  12. Yang X, Tan Y, Li K, Zhang H, Liu J et al. Long-term changes in summer phytoplankton communities and their influencing factors in Daya Bay, China (1991-2017). Mar Pollut Bull 2020; 161:111694 [View Article] [PubMed]
    [Google Scholar]
  13. Ausubel F, Brent R, Kingston RE, Moore DD, Seidman JG. eds Short protocols in molecular biology: a compendium of methods from current protocols in molecular biology. New York: Wiley; 1885
    [Google Scholar]
  14. Sun H, Hu Y, Zhou S, Zheng Y, Zhang XH. Glycocaulis profundi sp. nov., a marine bacterium isolated from seawater of the Mariana Trench. Int J Syst Evol Microbiol 2020; 70:814–819 [View Article] [PubMed]
    [Google Scholar]
  15. Yoon S-H, Ha S-M, Kwon S, Lim J, Kim Y et al. Introducing EzBioCloud: a taxonomically united database of 16S rRNA gene sequences and whole-genome assemblies. Int J Syst Evol Microbiol 2017; 67:1613–1617 [View Article] [PubMed]
    [Google Scholar]
  16. Larkin MA, Blackshields G, Brown NP, Chenna R, McGettigan PA et al. Clustal W and Clustal X version 2.0. Bioinformatics 2007; 23:2947–2948 [View Article] [PubMed]
    [Google Scholar]
  17. Saitou N, Nei M. The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 1987; 4:406–425 [View Article] [PubMed]
    [Google Scholar]
  18. Felsenstein J. Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol 1981; 17:368–376 [View Article] [PubMed]
    [Google Scholar]
  19. Fitch WM. Toward defining the course of evolution: minimum change for a specific tree topology. Systematic Zoology 1971; 20:406 [View Article]
    [Google Scholar]
  20. Kumar S, Stecher G, Li M, Knyaz C, Tamura K. MEGA X: Molecular Evolutionary Genetics Analysis across computing platforms. Mol Biol Evol 2018; 35:1547–1549 [View Article] [PubMed]
    [Google Scholar]
  21. 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] [PubMed]
    [Google Scholar]
  22. Wang X, Guo F, Tian P, Yu S, Xue C-X et al. Flammeovirga agarivorans sp. nov., an agar-digesting marine bacterium isolated from surface seawater. Int J Syst Evol Microbiol 2020; 70:6060–6066 [View Article] [PubMed]
    [Google Scholar]
  23. Beveridge TJ, Lawrence JR, Murray RG. Sampling and staining for light microscopy. In Methods for General and Molecular Microbiology, 3rd ed. American Society of Microbiology; 2007 pp 19–33
    [Google Scholar]
  24. Bernardet J-F, Nakagawa Y, Holmes B. Proposed minimal standards for describing new taxa of the family Flavobacteriaceae and emended description of the family. Int J Syst Evol Microbiol 2002; 52:1049–1070 [View Article] [PubMed]
    [Google Scholar]
  25. Tindall BJ, Sikorski J, Smibert RA, Krieg NR. Phenotypic characterization and the principles of comparative systematics. In Methods for General and Molecular Microbiology, 3rd ed. American Society of Microbiology; 2007 pp 330–393
    [Google Scholar]
  26. Yoon J-H, Lee K-C, Kho YH, Kang KH, Kim C-J et al. Halomonas alimentaria sp. nov., isolated from jeotgal, a traditional Korean fermented seafood. Int J Syst Evol Microbiol 2002; 52:123–130 [View Article] [PubMed]
    [Google Scholar]
  27. Sasser M. Identification of bacteria by gas chromatography of cellular fatty acids MIDI Technical Note 101. Newark DE: MIDI Inc; 1990
  28. Xie CH, Yokota A. Phylogenetic analyses of Lampropedia hyalina based on the 16S rRNA gene sequence. J Gen Appl Microbiol 2003; 49:345–349 [View Article] [PubMed]
    [Google Scholar]
  29. Minnikin DE, O’Donnell AG, Goodfellow M, Alderson G, Athalye M et al. An integrated procedure for the extraction of bacterial isoprenoid quinones and polar lipids. J Microbiol Methods 1984; 2:233–241 [View Article]
    [Google Scholar]
  30. Collins MD, Shah HN. Fatty acid, menaquinone and polar lipid composition of Rothia dentocariosa. Arch Microbiol 1984; 137:247–249 [View Article]
    [Google Scholar]
  31. Komagata K, Suzuki K-I. 4 Lipid and cell-wall analysis in bacterial systematics. In Methods in Microbiology Elsevier; 1988 pp 161–207
    [Google Scholar]
  32. Moore E, Arnscheidt A, Krüger A, Strömpl C, Mau M. Simplified protocols for the preparation of genomic DNA from bacterial cultures. Molecular Microbial Ecology Manual 1999; 1:1–15
    [Google Scholar]
  33. Luo R, Liu B, Xie Y, Li Z, Huang W et al. SOAPdenovo2: an empirically improved memory-efficient short-read de novo assembler. Gigascience 2012; 1:18 [View Article] [PubMed]
    [Google Scholar]
  34. Delcher AL, Bratke KA, Powers EC, Salzberg SL. Identifying bacterial genes and endosymbiont DNA with Glimmer. Bioinformatics 2007; 23:673–679 [View Article] [PubMed]
    [Google Scholar]
  35. Lagesen K, Hallin P, Rødland EA, Staerfeldt H-H, Rognes T et al. RNAmmer: consistent and rapid annotation of ribosomal RNA genes. Nucleic Acids Res 2007; 35:3100–3108 [View Article] [PubMed]
    [Google Scholar]
  36. Lowe TM, Eddy SR. tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res 1997; 25:955–964 [View Article] [PubMed]
    [Google Scholar]
  37. Gardner PP, Daub J, Tate JG, Nawrocki EP, Kolbe DL et al. Rfam: updates to the RNA families database. Nucleic Acids Res 2009; 37:D136–40 [View Article] [PubMed]
    [Google Scholar]
  38. Kim D, Park S, Chun J. Introducing EzAAI: a pipeline for high throughput calculations of prokaryotic average amino acid identity. J Microbiol 2021; 59:476–480 [View Article] [PubMed]
    [Google Scholar]
  39. Montero-Calasanz MDC, Göker M, Rohde M, Spröer C, Schumann P et al. Chryseobacterium hispalense sp. nov., a plant-growth-promoting bacterium isolated from a rainwater pond in an olive plant nursery, and emended descriptions of Chryseobacterium defluvii, Chryseobacterium indologenes, Chryseobacterium wanjuense and Chryseobacterium gregarium. Int J Syst Evol Microbiol 2013; 63:4386–4395 [View Article]
    [Google Scholar]
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