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MeSH Review

Acetobacterium

 
 
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Disease relevance of Acetobacterium

 

High impact information on Acetobacterium

  • Mechanism of anaerobic ether cleavage: conversion of 2-phenoxyethanol to phenol and acetaldehyde by Acetobacterium sp [3].
  • Chemiosmotic energy conservation with Na(+) as the coupling ion during hydrogen-dependent caffeate reduction by Acetobacterium woodii [4].
  • The Moorella thermoacetica aromatic O-demethylase was characterized as an inducible three-component system with similarity to the methanogenic methanol, methylamine, and methanethiol methyltransferases and to the O-demethylase system from Acetobacterium dehalogenans [5].
  • The objective of this study was to evaluate the effect of hydroxocobalamin (OH-Cbl) on transformation of high concentrations of carbon tetrachloride (CT) by Acetobacterium woodii (ATCC 29683) [6].
  • Sequence of subunit c of the Na(+)-translocating F1F0 ATPase of Acetobacterium woodii: proposal for determinants of Na+ specificity as revealed by sequence comparisons [7].
 

Chemical compound and disease context of Acetobacterium

 

Gene context of Acetobacterium

References

  1. Transformation of tetrachloroethylene to trichloroethylene by homoacetogenic bacteria. Terzenbach, D.P., Blaut, M. FEMS Microbiol. Lett. (1994) [Pubmed]
  2. Anaerobic biodegradation of methyl esters by Acetobacterium woodii and Eubacterium limosum. Liu, S., Suflita, J.M. J. Ind. Microbiol. (1994) [Pubmed]
  3. Mechanism of anaerobic ether cleavage: conversion of 2-phenoxyethanol to phenol and acetaldehyde by Acetobacterium sp. Speranza, G., Mueller, B., Orlandi, M., Morelli, C.F., Manitto, P., Schink, B. J. Biol. Chem. (2002) [Pubmed]
  4. Chemiosmotic energy conservation with Na(+) as the coupling ion during hydrogen-dependent caffeate reduction by Acetobacterium woodii. Imkamp, F., Müller, V. J. Bacteriol. (2002) [Pubmed]
  5. Characterization of a three-component vanillate O-demethylase from Moorella thermoacetica. Naidu, D., Ragsdale, S.W. J. Bacteriol. (2001) [Pubmed]
  6. Enhanced biotransformation of carbon tetrachloride by Acetobacterium woodii upon addition of hydroxocobalamin and fructose. Hashsham, S.A., Freedman, D.L. Appl. Environ. Microbiol. (1999) [Pubmed]
  7. Sequence of subunit c of the Na(+)-translocating F1F0 ATPase of Acetobacterium woodii: proposal for determinants of Na+ specificity as revealed by sequence comparisons. Rahlfs, S., Müller, V. FEBS Lett. (1997) [Pubmed]
  8. Sodium dependence of acetate formation by the acetogenic bacterium Acetobacterium woodii. Heise, R., Müller, V., Gottschalk, G. J. Bacteriol. (1989) [Pubmed]
  9. Tetrahydrofolate enzyme levels in Acetobacterium woodii and their implication in the synthesis of acetate from CO2. Tanner, R.S., Wolfe, R.S., Ljungdahl, L.G. J. Bacteriol. (1978) [Pubmed]
  10. Fermentative degradation of nonionic surfactants and polyethylene glycol by enrichment cultures and by pure cultures of homoacetogenic and propionate-forming bacteria. Wagener, S., Schink, B. Appl. Environ. Microbiol. (1988) [Pubmed]
  11. Isolation of carbon monoxide dehydrogenase from Acetobacterium woodii and comparison of its properties with those of the Clostridium thermoaceticum enzyme. Ragsdale, S.W., Ljungdahl, L.G., DerVartanian, D.V. J. Bacteriol. (1983) [Pubmed]
  12. A sodium-stimulated ATP synthase in the acetogenic bacterium Acetobacterium woodii. Heise, R., Reidlinger, J., Müller, V., Gottschalk, G. FEBS Lett. (1991) [Pubmed]
  13. Carbonic anhydrase in Acetobacterium woodii and other acetogenic bacteria. Braus-Stromeyer, S.A., Schnappauf, G., Braus, G.H., Gössner, A.S., Drake, H.L. J. Bacteriol. (1997) [Pubmed]
  14. Purification of ATP synthase from Acetobacterium woodii and identification as a Na(+)-translocating F1F0-type enzyme. Reidlinger, J., Müller, V. Eur. J. Biochem. (1994) [Pubmed]
  15. Anaerobic biodegradation of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) by Acetobacterium malicum strain HAAP-1 isolated from a methanogenic mixed culture. Adrian, N.R., Arnett, C.M. Curr. Microbiol. (2004) [Pubmed]
 
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