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High impact information on Methanospirillum


Anatomical context of Methanospirillum


Associations of Methanospirillum with chemical compounds


Gene context of Methanospirillum


Analytical, diagnostic and therapeutic context of Methanospirillum


  1. Biochemical evidence for formate transfer in syntrophic propionate-oxidizing cocultures of Syntrophobacter fumaroxidans and Methanospirillum hungatei. de Bok, F.A., Luijten, M.L., Stams, A.J. Appl. Environ. Microbiol. (2002) [Pubmed]
  2. Pathway of propionate oxidation by a syntrophic culture of Smithella propionica and Methanospirillum hungatei. de Bok, F.A., Stams, A.J., Dijkema, C., Boone, D.R. Appl. Environ. Microbiol. (2001) [Pubmed]
  3. Metabolism of benzoate, cyclohex-1-ene carboxylate, and cyclohexane carboxylate by "Syntrophus aciditrophicus" strain SB in syntrophic association with H(2)-using microorganisms. Elshahed, M.S., Bhupathiraju, V.K., Wofford, N.Q., Nanny, M.A., McInerney, M.J. Appl. Environ. Microbiol. (2001) [Pubmed]
  4. Culturable populations of Sporomusa spp. and Desulfovibrio spp. in the anoxic bulk soil of flooded rice microcosms. Rosencrantz, D., Rainey, F.A., Janssen, P.H. Appl. Environ. Microbiol. (1999) [Pubmed]
  5. Characterization of the anaerobic propionate-degrading syntrophs Smithella propionica gen. nov., sp. nov. and Syntrophobacter wolinii. Liu, Y., Balkwill, D.L., Aldrich, H.C., Drake, G.R., Boone, D.R. Int. J. Syst. Bacteriol. (1999) [Pubmed]
  6. Spheroplasts of Methanospirillum hungatii formed upon treatment with dithiothreitol. Sprott, G.D., Colvin, J.R., McKellar, R.C. Can. J. Microbiol. (1979) [Pubmed]
  7. Relationship of formate to growth and methanogenesis by Methanococcus thermolithotrophicus. Belay, N., Sparling, R., Daniels, L. Appl. Environ. Microbiol. (1986) [Pubmed]
  8. Coupling of methyl coenzyme M reduction with carbon dioxide activation in extracts of Methanobacterium thermoautotrophicum. Romesser, J.A., Wolfe, R.S. J. Bacteriol. (1982) [Pubmed]
  9. Characterization of novel, phenol-soluble polypeptides which confer rigidity to the sheath of Methanospirillum hungatei GP1. Southam, G., Beveridge, T.J. J. Bacteriol. (1992) [Pubmed]
  10. Growth of the syntrophic anaerobic acetogen, strain PA-1, with glucose or succinate as energy source. Brulla, W.J., Bryant, M.P. Appl. Environ. Microbiol. (1989) [Pubmed]
  11. Formation of unilamellar liposomes from total polar lipid extracts of methanogens. Choquet, C.G., Patel, G.B., Beveridge, T.J., Sprott, G.D. Appl. Environ. Microbiol. (1992) [Pubmed]
  12. Dichloromethane as the sole carbon source for an acetogenic mixed culture and isolation of a fermentative, dichloromethane-degrading bacterium. Braus-Stromeyer, S.A., Hermann, R., Cook, A.M., Leisinger, T. Appl. Environ. Microbiol. (1993) [Pubmed]
  13. Dissolution and immunochemical analysis of the sheath of the archaeobacterium Methanospirillum hungatei GP1. Southam, G., Beveridge, T.J. J. Bacteriol. (1991) [Pubmed]
  14. Acetic acid and hydrogen metabolism during coculture of an acetic acid producing bacterium with methanogenic bacteria. Patel, G.B., Roth, L.A. Can. J. Microbiol. (1978) [Pubmed]
  15. Energetics of syntrophic propionate oxidation in defined batch and chemostat cocultures. Scholten, J.C., Conrad, R. Appl. Environ. Microbiol. (2000) [Pubmed]
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