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Title: Acetate catabolism by Methanosarcina barkeri

Conference · · Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:6062189

Cell suspensions of Methanosarcina barkeri convert the carboxyl and methyl group carbons of acetate to carbon dioxide and methane at pH 6 under an atmosphere of 100% CO/sub 2/. The rate of loss of radioactivity from (1-/sup 14/C)acetate was over three times greater than that from (2-/sup 14/C)acetate under these conditions. Control experiments with both labeled substrates present showed that the rates were additive. Addition of a high level of 2-bromoethanesulfonate to selectively inhibit methane formation largely inhibited release of /sup 14/C from methyl-labeled acetate but only marginally decreased the rate of loss from (1-/sup 14/C)acetate. Thus, in the absence of the inhibitor loss of /sup 14/C from (1-/sup 14/C)acetate likely reflects an isotopic exchange reaction with CO/sub 2/ superimposed on the overall conversion of acetate to CO/sub 2/ and CH/sub 4/. The exchange reaction was inhibited by uncouplers such as 2,4-dinitrophenol, CCCP, and FCCP. Cells permeabilized by treatment with nonionic detergents or disrupted by passage through a French pressure cell failed to catalyze the exchange reaction. Exchange activity was not restored by addition of ATP or by use of (1-/sup 14/C)acetyl CoA as substrate. No evidence for involvement of carbon monoxide dehydrogenase in the exchange was found in these experiments when CO/sub 2/ was replaced by CO. However, the soluble extracts retained the ability to convert acetate to methane in the presence of H/sub 2/ and ATP.

Research Organization:
National Institute of Health, Bethesda, MD
OSTI ID:
6062189
Report Number(s):
CONF-870644-; TRN: 87-036543
Journal Information:
Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States), Vol. 46:6; Conference: 78. annual meeting of the American Society of Biological Chemists conference, Philadelphia, PA, USA, 7 Jun 1987
Country of Publication:
United States
Language:
English

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