1887

Abstract

A Gram-stain-negative marine bacterium, designated as WX04, was isolated from the South China Sea. The genome of strain WX04 contained a complete photosynthetic gene cluster and is the first identified photoheterotroph of the genus with high photochemical efficiency (Fv/Fm=0.705±0.010), indicating its diverse metabolic and growth strategies, and unique evolution in the genus . The genome size of strain WX04 is 3.78 Mbp, and the G+C content is 58.8 %. Its isolate formed pink colonies and the cells were non-flagellated and rod-shaped. Growth was observed at 15–35 °C (optimum, 30 °C), at pH 5.0–11.0 (optimum, pH 7.0) and in the presence of 3–5 % (w/v) NaCl (optimum, 3 %). Both catalase activity and oxidase activity were found to be negative. The 16S rRNA gene sequence analyses revealed that this isolate represents a novel species within the genus , sharing 96.8 and 95.6% sequence identities with DSM 15283 and DSM 26895, respectively. The respiratory quinone was ubiquinone-10 (100 %). The primary cellular fatty acids (>5 %) were summed feature 8 (C 7 and/or C 6), C,C 7 11-methyl and C 3-OH. The dominant polar lipids of strain WX04 comprised phosphatidylcholine, phosphatidylethanolamine and phosphatidylglycerol. The combined polyphasic data shows that strain WX04 is a novel species within the genus , which is proposed as sp. nov., and the type strain is WX04 (=KCTC 62628=MCCC 1K02295).

Funding
This study was supported by the:
  • National Key Research Programs (Award 2018YFA0605800)
    • Principle Award Recipient: QiChen
  • Cross strait postdoctoral exchange and funding program of Fujian Province (Award K8318001)
    • Principle Award Recipient: Ta-HuiLin
  • Fundamental Research Funds for the Central Universities (Award 20720190095)
    • Principle Award Recipient: NotApplicable
  • National Natural Science Foundation of China (Award 41776145, 41876150, 91751207 and 41861144018)
    • Principle Award Recipient: NotApplicable
Loading

Article metrics loading...

/content/journal/ijsem/10.1099/ijsem.0.005859
2023-05-12
2024-05-01
Loading full text...

Full text loading...

References

  1. Simon M, Scheuner C, Meier-Kolthoff JP, Brinkhoff T, Wagner-Döbler I et al. Phylogenomics of Rhodobacteraceae reveals evolutionary adaptation to marine and non-marine habitats. ISME J 2017; 11:1483–1499 [View Article] [PubMed]
    [Google Scholar]
  2. Luo H, Moran MA. Evolutionary ecology of the marine Roseobacter clade. Microbiol Mol Biol Rev 2014; 78:573–587 [View Article] [PubMed]
    [Google Scholar]
  3. Allgaier M, Uphoff H, Felske A, Wagner-Döbler I. Aerobic anoxygenic photosynthesis in Roseobacter clade bacteria from diverse marine habitats. Appl Environ Microbiol 2003; 69:5051–5059 [View Article] [PubMed]
    [Google Scholar]
  4. Brinkhoff T, Giebel HA, Simon M. Diversity, ecology, and genomics of the Roseobacter clade: a short overview. Arch Microbiol 2008; 189:531–539 [View Article] [PubMed]
    [Google Scholar]
  5. Jiao N, Zhang F, Hong N. Significant roles of bacteriochlorophylla supplemental to chlorophylla in the ocean. ISME J 2010; 4:595–597 [View Article] [PubMed]
    [Google Scholar]
  6. Liu Y, Zheng Q, Lin W, Jiao N. Characteristics and evolutionary analysis of photosynthetic gene clusters on extrachromosomal replicons: from streamlined plasmids to chromids. mSystems 2019; 4:e00358-19 [View Article] [PubMed]
    [Google Scholar]
  7. Choi DH, Cho BC. Shimia marina gen. nov., sp. nov., a novel bacterium of the Roseobacter clade isolated from biofilm in a coastal fish farm. Int J Syst Evol Microbiol 2006; 56:1869–1873 [View Article] [PubMed]
    [Google Scholar]
  8. Chen MH, Sheu SY, Chen CA, Wang JT, Chen WM. Shimia isoporae sp. nov., isolated from the reef-building coral Isopora palifera. Int J Syst Evol Microbiol 2011; 61:823–827 [View Article] [PubMed]
    [Google Scholar]
  9. Hameed A, Shahina M, Lin S-Y, Lai W-A, Hsu Y-H et al. Shimia biformata sp. nov., isolated from surface seawater, and emended description of the genus Shimia Choi and Cho 2006. Int J Syst Evol Microbiol 2013; 63:4533–4539 [View Article] [PubMed]
    [Google Scholar]
  10. Hyun D-W, Kim M-S, Shin N-R, Kim JY, Kim PS et al. Shimia haliotis sp. nov., a bacterium isolated from the gut of an abalone, Haliotis discus hannai. Int J Syst Evol Microbiol 2013; 63:4248–4253 [View Article] [PubMed]
    [Google Scholar]
  11. Zhu S, Chen C, Cheng Y, Guo C, Peng N et al. Shimia sediminis sp. nov., a bacterium isolated from marine sediment in the East China Sea. Int J Syst Evol Microbiol 2021; 71: [View Article] [PubMed]
    [Google Scholar]
  12. Guillard RR, Ryther JH. Studies of marine planktonic diatoms. I. Cyclotella nana Hustedt, and Detonula confervacea (cleve) Gran. Can J Microbiol 1962; 8:229–239 [View Article] [PubMed]
    [Google Scholar]
  13. Embley TM. The linear PCR reaction: a simple and robust method for sequencing amplified rRNA genes. Lett Appl Microbiol 1991; 13:171–174 [View Article] [PubMed]
    [Google Scholar]
  14. Chun J, Lee J-H, Jung Y, Kim M, Kim S et al. EzTaxon: a web-based tool for the identification of prokaryotes based on 16S ribosomal RNA gene sequences. Int J Syst Evol Microbiol 2007; 57:2259–2261 [View Article] [PubMed]
    [Google Scholar]
  15. Kim O-S, Cho Y-J, Lee K, Yoon S-H, Kim M et al. Introducing EzTaxon-e: a prokaryotic 16S rRNA gene sequence database with phylotypes that represent uncultured species. Int J Syst Evol Microbiol 2012; 62:716–721 [View Article] [PubMed]
    [Google Scholar]
  16. Thompson JD, Higgins DG, Gibson TJ. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 1994; 22:4673–4680 [View Article] [PubMed]
    [Google Scholar]
  17. Felsenstein J. Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol 1981; 17:368–376 [View Article] [PubMed]
    [Google Scholar]
  18. Rzhetsky A, Nei M. Statistical properties of the ordinary least-squares, generalized least-squares, and minimum-evolution methods of phylogenetic inference. J Mol Evol 1992; 35:367–375 [View Article] [PubMed]
    [Google Scholar]
  19. 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]
  20. Rodríguez-R L, Konstantinidis K. Bypassing cultivation to identify bacterial species: culture-independent genomic approaches identify credibly distinct clusters, avoid cultivation bias, and provide true insights into microbial species. Microbe Mag 2014; 9:111–118
    [Google Scholar]
  21. Xu L, Sun C, Fang C, Oren A, Xu XW. Genomic-based taxonomic classification of the family Erythrobacteraceae. Int J Syst Evol Microbiol 2020; 70:4470–4495 [View Article] [PubMed]
    [Google Scholar]
  22. 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] [PubMed]
    [Google Scholar]
  23. Bowman JP. Description of Cellulophaga algicola sp. nov., isolated from the surfaces of Antarctic algae, and reclassification of Cytophaga uliginosa (ZoBell and Upham 1944) Reichenbach 1989 as Cellulophaga uliginosa comb. nov. Int J Syst Evol Microbiol 2000; 50 Pt 5:1861–1868 [View Article] [PubMed]
    [Google Scholar]
  24. Sun F, Wang B, Du Y, Liu X, Lai Q et al. Arenibacter nanhaiticus sp. nov., isolated from marine sediment of the South China Sea. Int J Syst Evol Microbiol 2010; 60:78–83 [View Article] [PubMed]
    [Google Scholar]
  25. Kates M. eds Techniques of Lipidology: Isolation, Analysis, and Identification of Lipids Newport Somerville; 2010
    [Google Scholar]
  26. Miller LT. Single derivatization method for routine analysis of bacterial whole-cell fatty acid methyl esters, including hydroxy acids. J Clin Microbiol 1982; 16:584–586 [View Article] [PubMed]
    [Google Scholar]
  27. Sasser M. MIDI technical note 101. Identification of bacteria by gas chromatography of cellular fatty acids MIDI, Newark. DE: 1990 pp 1–7
    [Google Scholar]
  28. Collins MD. 11 Analysis of isoprenoid quinones. In Bergan T. eds Methods in Microbiology Academic Press; 1985 pp 329–366
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/ijsem/10.1099/ijsem.0.005859
Loading
/content/journal/ijsem/10.1099/ijsem.0.005859
Loading

Data & Media loading...

Supplements

Supplementary material 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