Skip to main content
Log in

Pelagibacterium nitratireducens sp.nov., A Marine Alphaproteobacterium Isolated from the East China Sea

  • Published:
Current Microbiology Aims and scope Submit manuscript

Abstract

A Gram-negative, rod-shaped, non-spore-forming aerobic bacterium, motile with a single polar flagellum, strain JLT2005T, was isolated from surface seawater collected from the East China Sea and formed ivory white colonies on a rich organic medium. The strain was positive for catalase, oxidase, and urease. It grew in the presence of 0–12 % (w/v) NaCl (optimum 5 %), at 20–35 °C (optimum 25 °C), or at pH 6–10 (optimum pH 9). The major fatty acids (>10 %) were C18:1ω7c, C19:0ω8c cyclo, C16:0, and C18:0. The major polar lipids were phosphatidylglycerol, diphosphatidylglycerol, and five unidentified glycolipids. Ubiquinone-10 and Ubiquinone-11 were present as the major quinones. The DNA G+C content was 74.3 mol%. Phylogenetic analyses based on 16S rRNA gene sequences indicated that strain JLT2005T belongs to the genus Pelagibacterium in the family Hyphomicrobiaceae, class Alphaproteobacteria. The closest neighbors were Pelagibacterium halotolerans B2T (98.7 % similarity) and Pelagibacterium luteolum 1_C16_27T (97.1 % similarity). DNA–DNA relatedness values of strain JLT2005T with P. halotolerans B2T and with P. luteolum 1_C16_27T were 31.6 and 25 %. Evidence from genotypic, chemotaxonomic, and phenotypic data shows that strain JLT2005T represents a novel species of the genus Pelagibacterium, for which the name Pelagibacterium nitratireducens sp. nov is proposed. The type strain is JLT2005T (=CGMCC 1.10829T =JCM 17767T).

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Xu X-W, Huo Y–Y, Wang C-S, Oren A, Cui H-L, Vedler E, Wu M (2011) Pelagibacterium halolerans gen.nov., sp. nov. and Pelagibacterium luteolum sp. nov., novel members of the family Hyphomicrobiaceae. Int J Syst Evol Microbiol 61:1817–1822

    Article  PubMed  CAS  Google Scholar 

  2. Drews G (1983) Mikrobiologisches Praktikum (in German). Springer, Berlin

    Book  Google Scholar 

  3. Yurkov VV, Krieger S, Stackebrandt E, Beatty JT (1999) Citromicrobium bathyomarinum, a novel aerobic bacterium isolated from deep-sea hydrothermal vent plume waters that contains photosynthetic pigment-protein complexes. J Bacteriol 181(15):4517–4525

    PubMed  CAS  Google Scholar 

  4. Gerhardt P, Murray RGE, Wood WA, Krieg NR (eds) (1994) Methods for general and molecular bacteriology. American Society for Microbiology, Washington, DC

    Google Scholar 

  5. Dong X-Z, Cai M-Y (2001) Determinative manual for routine bacteriology. Scientific, Beijing

    Google Scholar 

  6. Clarke PH (1953) Hydrogen sulphide production by bacteria. J Gen Microbiol 8:397–407

    PubMed  CAS  Google Scholar 

  7. Mata JA, Martínez-Cánovas J, Quesada E, Béjar V (2002) A detailed phenotypic characterisation of the type strains of Halomonas species. Syst Appl Microbiol 25:360–375

    Article  PubMed  CAS  Google Scholar 

  8. Barritt MM (1936) The intensification of the Voges-Proskauer reaction by the addition of a-naphthol. J Pathol Bacteriol 42:441–445

    Article  CAS  Google Scholar 

  9. Leifson E (1963) Determination of carbohydrate metabolism of marine bacteria. J Bacteriol 85:1183–1184

    PubMed  CAS  Google Scholar 

  10. Xu X-W, Wu Y-H, Wang C-S, Yang J-Y, Oren A, Wu M (2008) Marinobacter pelagius sp. nov. a moderately halophilic bacterium. Int J Syst Evol Microbiol 58:637–640

    Article  PubMed  CAS  Google Scholar 

  11. Hiraishi A, Ueda Y, Ishihara J (1998) Quinone profiling of bacterial communities in natural and synthetic sewage activated sludge for enhanced phosphate removal. App Environ Microbiol 64:992–998

    CAS  Google Scholar 

  12. Romano I, Lama L, Nicolaus B, Poli A, Gambacorta A, Giordano A (2006) Halomonas alkaliphila sp. nov., a novel halotolerant alkaliphilic bacterium isolated from a salt pool in Campania (Italy). J Gen Appl Microbiol 52:339–348

    Article  PubMed  CAS  Google Scholar 

  13. Kates M (1986) Techniques of Lipidology, 2nd edn. Elsevier, Amsterdam

    Google Scholar 

  14. Marmur J (1961) A procedure for the isolation of deoxyribonucleic acid from microorganisms. J Mol Biol 3:208–218

    Article  CAS  Google Scholar 

  15. Johnson JL (1994) Similarity analysis of DNAs. In: P. E. Gerhardt, R. G. Murray, W. A. Wood & N. R. Krieg (eds) Methods for general and molecular bacteriology, pp 655–681

  16. Marmur J, Doty P (1962) Determination of the base composition of DNA from its thermal denaturation temperature. J Mol Biol 5:109–118

    Article  PubMed  CAS  Google Scholar 

  17. De Ley J (1970) Reexamination of the association between melting point, buoyant density, and chemical base composition of deoxyribonucleic acid. J Bacteriol 101:738–754

    PubMed  Google Scholar 

  18. Embley TM (1991) The linear PCR reaction: a simple and robust method for sequencing amplified rRNA genes. Lett Appl Microbiol 13:171–174

    Article  PubMed  CAS  Google Scholar 

  19. Thompson JD, Higgins DG, Gibson TJ (1994) CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 22:4673–4680

    Article  PubMed  CAS  Google Scholar 

  20. Chun J, Lee J-H, Jung Y, Kim M, Kim BK, Lim Y-W (2007) EzTaxon: a web-based tool for the identification of prokaryotes based on 16S ribosomal RNA gene sequences. Int J Syst Evol Microbiol 57:2259–2261

    Article  PubMed  CAS  Google Scholar 

  21. Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S (2011) MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 28:2731–2739

    Article  PubMed  CAS  Google Scholar 

  22. De Ley J, Cattoir H, Reynaerts A (1970) The quantitative measurement of DNA hybridization from renaturation rates. Eur J Biochem 12:133–142

    Article  PubMed  Google Scholar 

  23. Stackebrandt E, Goebel BM (1994) Taxonomic note: a place for DNA–DNA reassociation and 16S rRNA sequence analysis in the present species definition in bacteriology. Int J Syst Bacteriol 44:846–849

    Article  CAS  Google Scholar 

Download references

Acknowledgments

The authors would like to thank Dr. Yanan Wang, Key Laboratory of Microbial Engineering at the Institute of Biology, Henan Academy of Sciences; Dr. Xiaojun Yan, School of Life Science & Biological Engineering, Ningbo University; Dr. Henglin Cui, School of Food & Biological Engineering, Jiangsu University; and Dr. Li Gu, Third Institute of Oceanography, State Oceanic Administration for their valuable assistance. Professor John Hodgkiss is also thanked for his assistance with English. This work was supported by 973 program (2011CB808800), SOA project (201105021), MOST project (2012AA092003), and NSFC (41191021). Dr. Rui Zhang was also supported by NSFC (40906059).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Rui Zhang.

Electronic Supplementary Material

Below is the link to the electronic supplementary material.

Supplementary material 1 (DOC 497 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Li, Q., Xu, Y., Liu, K. et al. Pelagibacterium nitratireducens sp.nov., A Marine Alphaproteobacterium Isolated from the East China Sea. Curr Microbiol 66, 450–455 (2013). https://doi.org/10.1007/s00284-012-0299-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00284-012-0299-9

Keywords

Navigation