Skip to main content
Log in

Isolation and characterization ofMethanobrevibacter oralis sp. nov.

  • Published:
Current Microbiology Aims and scope Submit manuscript

Abstract

A new coccobacillary, nonmotile, Gram-positive, methane-producing organism was isolated from human subgingival plaque. Both hydrogen and carbon dioxide were required for growth. No methane was produced from acetate, formate, or methanol. The optimum pH was 6.9–7.4, and the optimum temperature was 36–38°C. Fecal extract was required for growth, and a volatile fatty acid mixture was highly stimulatory. The DNA G+C content was 28 mol%. On the basis of these characteristics, DNA-DNA hybridization studies, and electrophoretic analysis of cellular proteins, the isolate was considered a new species and namedMethanobrevibacter oralis.

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.

Similar content being viewed by others

Literature Cited

  1. Balch WE, Fox GE, Magnum LJ, Woese CR, Wolfe RS (1979) Methanogens: reevaluations of a unique biological group. Microbiol Rev 43:260–296

    PubMed  Google Scholar 

  2. Barnes EM, Impey CS (1974) The occurrence and properties of uric acid decomposing anaerobic bacteria in the avian caecum. J Appl Bacteriol 37:393–409

    PubMed  Google Scholar 

  3. Belay N, Johnson R, Rajagopal BS, Conway de Macario E, Daniels L (1988) Methanogenic bacteria from human dental plaque. Appl Environ Microbiol 54:600–603

    PubMed  Google Scholar 

  4. Biavati B, Castagnoli P, Trovatelli LD (1986) Species of the genusBifidobacterium in the feces of human adults. Microbiologica 9:39–45

    PubMed  Google Scholar 

  5. Boone RD, Mah RA (1989) Methanogenic archaebacteria. In: Stanley JT, Bryant MP, Pfenning N, Holt JG (eds) Bergey's manual of systematic bacteriology. Baltimore: Williams and Wilkins, pp 2173–2216

    Google Scholar 

  6. Boone DR, Whitmann WB (1988) Proposal of minimal standard describing new taxa of methanogenic bacteria. Int J Syst Bacteriol 38:212–219

    Google Scholar 

  7. Brusa T, Conca R, Ferrara A, Ferrari A, Pecchioni A (1987) The presence of methanobacteria in human subgingival plaque. J Clin Periodontol 14:470–471

    PubMed  Google Scholar 

  8. Brusa T, Canzi E, Allievi L, Del Puppo E, Ferrari A (1993) Methanogens in the human intestinal tract and oral cavity. Curr Microbiol 27:261–265

    Google Scholar 

  9. DSM—Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (1989) Catalogue of strains, 4th ed, p 289

  10. Holdeman LV, Moore WEC (1973) Anaerobic laboratory manual, 4th ed., Virginia Polytechnic Institute and State University Anaerobe Laboratory

  11. Johnson JI (1985) DNA reassociation and RNA hybridization of bacterial nucleic acids. In: Gottschalk G (ed) Methods in microbiology, vol 18. New York: Academic Press, pp 33–74

    Google Scholar 

  12. Marmur J (1961) A procedure for the isolation of deoxyribonucleic acid from micro-organisms. J Mol Biol 3:208–218

    Google Scholar 

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

    PubMed  Google Scholar 

  14. Miller TL, Wolin MJ (1974) A serum bottle modification of the Hungate technique for cultivating obligate anaerobes. Appl Microbiol 27:985–987

    PubMed  Google Scholar 

  15. Miller TL, Wolin MJ (1982) Enumeration ofMethanobrevibacter smithii in human faeces. Arch Microbiol 131:14–18

    PubMed  Google Scholar 

  16. Miller TL, Wolin MJ (1985)Methanosphera stadmaniae gen. nov. sp. nov.; a species that forms methane by reducing methanol with hydrogen. Arch Microbiol 141:116–122

    PubMed  Google Scholar 

  17. Miller TL, Wolin MJ, Conway de Macario E, Macario AJL (1982) Isolation ofMethanobrevibacter smithii from human feces. Appl Environ Microbiol 43:227–232

    PubMed  Google Scholar 

  18. Moore WEC, Hasch DE, Holdeman LV, Cato, EP (1980) Polyacrylamide slab gel elecrophoresis of soluble proteins for studies of bacterial floras. Appl Environ Microbiol 39:900–907

    Google Scholar 

  19. Reynolds ES (1963) The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol 17:208–212

    PubMed  Google Scholar 

  20. Smith PH, Hungate RE (1958) Isolation and characterization ofMethanobacterium ruminantium n. sp. J Bacteriol 75:713–718

    PubMed  Google Scholar 

  21. Socransky SS, Gibson RJ, Dale AC, Bortmich L, Rosental E, MacDonald JB (1963) The microbiota of the gingival crevice area of man. Arch Oral Biol 8:275–280

    PubMed  Google Scholar 

  22. Taylor CD, McBride BC, Wolfe RS, Bryant MP (1974) Coenzyme M, essential for growth of a rumen strain ofMethanobacterium ruminantium. J Bacteriol 120:974–975

    PubMed  Google Scholar 

  23. Zeikus JG, Bowen VG (1975) Comparative ultrastructure of methanogenic bacteria. Can J Microbiol 21:121–129

    PubMed  Google Scholar 

  24. Zeikus JG, Henning DL (1975)Methanobacterium arboriphilicum sp. nov., an obligate anaerobe isolated from wetwood of living trees. Antonie van Leeuwenhoek 41:543–552

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ferrari, A., Brusa, T., Rutili, A. et al. Isolation and characterization ofMethanobrevibacter oralis sp. nov.. Current Microbiology 29, 7–12 (1994). https://doi.org/10.1007/BF01570184

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01570184

Keywords

Navigation