1887

Abstract

Five Gram-negative, white-pigmented, spherical, chemoheterotrophic bacteria were isolated from seawater from Japan and the Republic of Palau by use of an cultivation technique. Phylogenetic analyses based on 16S rRNA gene sequences indicated that the five novel isolates, 02PA-Ca-133, YM14-201, H-MN57, H-MN48 and MN1-156, were closely affiliated to members of subdivision 4 within the phylum ‘’. The novel isolates shared 96–100 % sequence similarity with each other and showed less than 90 % similarity with the cultivated strains of subdivision 4. DNA–DNA relatedness values between strains 02PA-Ca-133, YM14-201 and H-MN57 were less than 70 %; the value commonly accepted as the threshold for the phylogenetic definition of a species. Antibiotic susceptibility tests and amino acid analysis of cell-wall hydrolysates indicated that the novel isolates did not contain muramic acid or diaminopimelic acid in their cell walls, suggesting that these strains lack peptidoglycan. The DNA G+C contents of the five strains were 51–57 mol%. The major menaquinone was MK-7 and C, C 7 and anteiso-C were the major fatty acids. On the basis of polyphasic taxonomic evidence, it is concluded that these strains should be classified as representing a new genus and three novel species in subdivision 4 of the phylum ‘’, for which the names gen. nov., sp. nov. [type strain 02PA-Ca-133 (=MBIC08004=IAM 15422=KCTC 13126)], sp. nov. [type strain YM14-201 (=MBIC08272=IAM 15421=KCTC 13124)] and sp. nov. [type strain H-MN57 (=MBIC08273=IAM 15423=KCTC 13125)] are proposed.

Loading

Article metrics loading...

/content/journal/ijsem/10.1099/ijs.0.64970-0
2007-07-01
2024-04-23
Loading full text...

Full text loading...

/deliver/fulltext/ijsem/57/7/1377.html?itemId=/content/journal/ijsem/10.1099/ijs.0.64970-0&mimeType=html&fmt=ahah

References

  1. Chin K.-J., Liesack W., Janssen P. H. 2001; Opitutus terrae gen. nov., sp. nov., to accommodate novel strain of the division ‘ Verrucomicrobia ’ isolated from rice paddy soil. Int J Syst Evol Microbiol 51:1965–1968 [CrossRef]
    [Google Scholar]
  2. Dedysh S. N., Pankratov T. A., Belova S. E., Kulichevskaya I. S., Liesack W. 2006; Phylogenetic analysis and in situ identification of bacteria community composition in an acidic Sphagnum peat bog. Appl Environ Microbiol 72:2110–2117 [CrossRef]
    [Google Scholar]
  3. Ezaki T., Hashimoto Y., Yabuuchi E. 1989; Fluorometric deoxyribonucleic acid-deoxyribonucleic acid hybridization in microdilution wells as an alternative to membrane filter hybridization in which radioisotopes are used to determine genetic relatedness among bacterial strains. Int J Syst Bacteriol 39:224–229 [CrossRef]
    [Google Scholar]
  4. Felsenstein J. 1985; Confidence limits on phylogenies: an approach using the bootstrap. Evolution 39:783–791 [CrossRef]
    [Google Scholar]
  5. Harper J. J., Davis G. H. G. 1979; Two-dimensional thin-layer chromatography for amino acid analysis of bacterial cell walls. Int J Syst Bacteriol 29:56–58 [CrossRef]
    [Google Scholar]
  6. Haukka K., Heikkinen E., Kairesalo T., Karjalainen H., Sivonen K. 2005; Effect of humic material on the bacterioplankton community composition in boreal lakes and mesocosms. Environ Microbiol 7:620–630 [CrossRef]
    [Google Scholar]
  7. Haukka K., Kolmonen E., Hyder R., Hietala J., Vakkilainen K., Kairesalo T., Haario H., Sivonen K. 2006; Effect of nutrient loading on bacterioplankton community composition in lake mesocosms. Microb Ecol 51:137–146 [CrossRef]
    [Google Scholar]
  8. Hayakawa M., Nonomura H. 1987; Humic acid-vitamin agar, a new medium for the selective isolation of soil actinomycetes. J Ferment Technol 65:501–509 [CrossRef]
    [Google Scholar]
  9. Hedlund B. P., Gosink J. J., Staley J. T. 1997; Verrucomicrobia div. nov., a new division of the bacteria containing three new species of Prosthecobacter . Antonie van Leeuwenhoek 72:29–38 [CrossRef]
    [Google Scholar]
  10. Hugenholtz P., Goebel B. M., Pace N. R. 1998; Impact of culture-independent studies on the emerging phylogenetic view of bacterial diversity. J Bacteriol 180:4765–4774
    [Google Scholar]
  11. Joseph S. J., Hugenholtz P., Sangwan P., Osborne C. A., Janssen P. H. 2003; Laboratory cultivation of widespread and previously uncultured soil bacteria. Appl Environ Microbiol 69:7210–7215 [CrossRef]
    [Google Scholar]
  12. Kanokratana P., Chanapan S., Pootanakit K., Eurwilaichitr L. 2004; Diversity and abundance of Bacteria and Archaea in the Bor Khlueng hot spring in Thailand. J Basic Microbiol 44:430–444 [CrossRef]
    [Google Scholar]
  13. Katsuta A., Adachi K., Matsuda S., Shizuri Y., Kasai H. 2005; Ferrimonas marina sp. nov. Int J Syst Evol Microbiol 55:1851–1855 [CrossRef]
    [Google Scholar]
  14. Kumar S., Tamura K., Nei M. 2004; mega3: integrated software for molecular evolutionary genetics analysis and sequence alignment. Brief Bioinform 5:150–163 [CrossRef]
    [Google Scholar]
  15. Lyman J., Fleming R. H. 1940; Composition of sea water. J Mar Res 3:134–146
    [Google Scholar]
  16. Marmur J. 1961; A procedure for the isolation of deoxyribonucleic acid from micro-organisms. J Mol Biol 3:208–218 [CrossRef]
    [Google Scholar]
  17. Mesbah M., Premachandran U., Whitman W. B. 1989; Precise measurement of the G+C content of deoxyribonucleic acid by high-performance liquid chromatography. Int J Syst Bacteriol 39:159–167 [CrossRef]
    [Google Scholar]
  18. Murray R. G. E., Doetsch R. N., Robinow C. F. 1994; Determinative and cytological light microscopy. In Methods for General and Molecular Bacteriology pp  21–41 Edited by Gerhardt P., Murray R. G. E., Wood W. A., Krieg N. R. Washington, DC: American Society for Microbiology;
    [Google Scholar]
  19. Polymenakou P. N., Bertilsson S., Tselepides A., Stephanou E. G. 2005; Bacterial community composition in different sediments from the Eastern Mediterranean Sea: a comparison of four 16S ribosomal DNA clone libraries. Microb Ecol 50:447–462 [CrossRef]
    [Google Scholar]
  20. Rappé M. S., Giovannoni S. J. 2003; The uncultured microbial majority. Annu Rev Microbiol 57:369–394 [CrossRef]
    [Google Scholar]
  21. Sakai T., Ishizuka K., Kato I. 2003; Isolation and characterization of a fucoidan-degrading marine bacterium. Mar Biotechnol (NY) 5:409–416 [CrossRef]
    [Google Scholar]
  22. Sangwan P., Chen X., Hugenholtz P., Janssen P. H. 2004 Chthoniobacter flavus gen. nov., sp. nov., the first pure-culture representative of subdivision two, Spartobacteria classis nov., of the phylum Verrucomicrobia . Appl Environ Microbiol 705875–5881 [CrossRef]
  23. Scheuermayer M., Gulder T. A. M., Bringmann G., Hentschel U. 2006 Rubritalea marina gen. nov., sp. nov., a marine representative of the phylum ‘ Verrucomicrobia ’, isolated from a sponge ( Porifera ). Int J Syst Evol Microbiol 562119–2124 [CrossRef]
  24. Schleifer K. H., Kandler O. 1972; Peptidoglycan types of bacterial cell walls and their taxonomic implications. Bacteriol Rev 36:407–477
    [Google Scholar]
  25. Shieh W. Y., Jean W. D. 1998; Alterococcus agarolyticus , gen. nov., sp. nov. a halophilic thermophilic bacterium capable of agar degradation. Can J Microbiol 44:637–645 [CrossRef]
    [Google Scholar]
  26. Sikes D. S., Lewis P. O. 2001 Beta software, version 1. PAUPR at: PAUP implementation of the parsimony ratchet Department of Ecology and Evolutionary Biology, University of Connecticut, Storrs;
    [Google Scholar]
  27. Swofford D. L. 2002 paup*: Phylogenetic Analysis Using Parsimony (*and other methods Sunderland, MA: Sinauer Associates;
    [Google Scholar]
  28. Thompson J. D., Gibson T. J., Plewniak F., Jeanmougin F., Higgins D. G. 1997; The clustal_x windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 25:4876–4882 [CrossRef]
    [Google Scholar]
  29. Vandekerckhove T. T. M., Willems A., Gillis M., Coomans A. 2000; Occurrence of novel verrucomicrobial species, endosymbiotic and associated with parthenogenesis in Xiphinema americanum -group species (Nematoda, Longidoridae). Int J Syst Evol Microbiol 50:2197–2205 [CrossRef]
    [Google Scholar]
  30. Wayne L. G., Brenner D. J., Colwell R. R., Grimont P. A. D., Kandler O., Krichevsky M. I., Moore L. H., Moore W. E. C., Murray R. G. E. other authors 1987; International Committee on Systematic Bacteriology. Report of the ad hoc committee on reconciliation of approaches to bacterial systematics. Int J Syst Bacteriol 37:463–464 [CrossRef]
    [Google Scholar]
  31. Weisburg W. G., Barns S. M., Pelletier D. A., Lane D. J. 1991; 16S ribosomal DNA amplification for phylogenetic study. J Bacteriol 173:697–703
    [Google Scholar]
  32. Yasumoto-Hirose M., Nishijima M., Ngirchechol M. K., Kanoh K., Shizuri Y., Miki W. 2006; Isolation of marine bacteria by in situ culture on media-supplemented polyurethane foam. Mar Biotechnol (NY) 8227–237 [CrossRef]
    [Google Scholar]
  33. Yokota A., Tamura T., Nishii T., Hasegawa T. 1993 Kineococcus aurantiacus gen. nov., sp. nov., a new aerobic, gram-positive, motile coccus with meso -diaminopimelic acid and arabinogalactan in the cell wall. Int J Syst Bacteriol 4352–57 [CrossRef]
  34. Yoon J., Yasumoto-Hirose M., Katsuta A., Sekiguchi H., Matsuda S., Kasai H., Yokota A. 2007; Coraliomargarita akajimensis gen. nov., sp. nov. a novel member of the phylum ‘ Verrucomicrobia ’ isolated from seawater in Japan. Int J Syst Evol Microbiol 57:959–963 [CrossRef]
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/ijsem/10.1099/ijs.0.64970-0
Loading
/content/journal/ijsem/10.1099/ijs.0.64970-0
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