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Stable carbon isotope fractionation by Methanosarcina barkeri during methanogenesis from acetate, methanol, or carbon dioxide-hydrogen

Journal Article · · Appl. Environ. Microbiol.; (United States)
OSTI ID:6970779
Methanosarcina barkeri was cultured on methanol, H/sub 2/-CO/sub 2/, and acetate, and the /sup 13/C//sup 12/C ratios of the substrates and the methane produced from them were determined. The discrimination against /sup 13/C in methane relative to substrate decreased in the order methanol > CO/sub 2/ > acetate. The isotopic fractionation for methane derived from acetate was only one-third of that observed with methanol as the substrate. The data presented indicate that the last enzyme of methanogenesis, methylreductase, is not the primary site of isotopic discrimination during methanogenesis from methanol or CO/sub 2/. These results also support biogeochemical interpretations that gas produced in environments in which acetate is the primary methane precursor will have higher /sup 13/C//sup 12/C ratios than those from environments where other substrates predominate.
Research Organization:
Univ. of Wisconsin, Madison (USA)
OSTI ID:
6970779
Journal Information:
Appl. Environ. Microbiol.; (United States), Journal Name: Appl. Environ. Microbiol.; (United States) Vol. 53:10; ISSN AEMID
Country of Publication:
United States
Language:
English