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. 1983 Apr;45(4):1411–1414. doi: 10.1128/aem.45.4.1411-1414.1983

Pathways of Propionate Degradation by Enriched Methanogenic Cultures

Markus Koch 1,, Jan Dolfing 1,, Karl Wuhrmann 1, Alexander J B Zehnder 1,
PMCID: PMC242473  PMID: 16346281

Abstract

A mixed methanogenic culture was highly enriched in a growth medium containing propionate as the sole organic carbon and energy source. With this culture, the pathways of propionate degradation were studied by use of 14C-radiotracers. Propionate was first metabolized to acetate, carbon dioxide, and hydrogen by nonmethanogenic organisms. Formate was not excreted. The carbon dioxide originated exclusively from the carboxyl group of propionate, whereas both [2-14C]- and [3-14C]propionate lead to the production of radioactive acetate. The methyl and carboxyl groups of the acetate produced were equally labeled, regardless of whether [2-14C]- or [3-14C]propionate was used. These observations suggest that in the culture, propionate was degraded through a randomizing pathway.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Boone D. R., Bryant M. P. Propionate-Degrading Bacterium, Syntrophobacter wolinii sp. nov. gen. nov., from Methanogenic Ecosystems. Appl Environ Microbiol. 1980 Sep;40(3):626–632. doi: 10.1128/aem.40.3.626-632.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. KAZIRO Y., OCHOA S. THE METABOLISM OF PROPIONIC ACID. Adv Enzymol Relat Areas Mol Biol. 1964;26:283–378. doi: 10.1002/9780470122716.ch7. [DOI] [PubMed] [Google Scholar]
  3. Kaspar H. F., Wuhrmann K. Kinetic parameters and relative turnovers of some important catabolic reactions in digesting sludge. Appl Environ Microbiol. 1978 Jul;36(1):1–7. doi: 10.1128/aem.36.1.1-7.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Kay W. W. Genetic control of the metabolism of propionate by Escherichia coli K12. Biochim Biophys Acta. 1972 May 16;264(3):508–521. doi: 10.1016/0304-4165(72)90014-1. [DOI] [PubMed] [Google Scholar]
  5. Miller T. L., Wolin M. J. Fermentations by saccharolytic intestinal bacteria. Am J Clin Nutr. 1979 Jan;32(1):164–172. doi: 10.1093/ajcn/32.1.164. [DOI] [PubMed] [Google Scholar]
  6. STADTMAN T. C., BARKER H. A. Studies on the methane fermentation. VIII. Tracer experiments of fatty acid oxidation by methane bacteria. J Bacteriol. 1951 Jan;61(1):67–80. doi: 10.1128/jb.61.1.67-80.1951. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Thauer R. K., Jungermann K., Decker K. Energy conservation in chemotrophic anaerobic bacteria. Bacteriol Rev. 1977 Mar;41(1):100–180. doi: 10.1128/br.41.1.100-180.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. WOLIN E. A., WOLIN M. J., WOLFE R. S. FORMATION OF METHANE BY BACTERIAL EXTRACTS. J Biol Chem. 1963 Aug;238:2882–2886. [PubMed] [Google Scholar]
  9. Zehnder A. J., Brock T. D. Methane formation and methane oxidation by methanogenic bacteria. J Bacteriol. 1979 Jan;137(1):420–432. doi: 10.1128/jb.137.1.420-432.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Zehnder A. J., Huser B. A., Brock T. D., Wuhrmann K. Characterization of an acetate-decarboxylating, non-hydrogen-oxidizing methane bacterium. Arch Microbiol. 1980 Jan;124(1):1–11. doi: 10.1007/BF00407022. [DOI] [PubMed] [Google Scholar]
  11. Zehnder A. J., Huser B., Brock T. D. Measuring radioactive methane with the liquid scintillation counter. Appl Environ Microbiol. 1979 May;37(5):897–899. doi: 10.1128/aem.37.5.897-899.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]

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