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Appl Environ Microbiol. 1986 January; 51(1): 84-87
Copyright © 1986, American Society for Microbiology. All Rights Reserved.

Anaerobic C1 Metabolism of the O-Methyl-14C-Labeled Substituent of Vanillate

Anne Cornish Frazer* and L. Y. Young

1 Department of Microbiology and Department of Environmental Medicine, 2 New York University Medical Center, New York, New York 10016

ABSTRACT

The O-methyl substituents of aromatic compounds constitute a C1 growth substrate for a number of taxonomically diverse anaerobic acetogens. In this study, strain TH-001, an O-demethylating obligate anaerobe, was chosen to represent this physiological group, and the carbon flow when cells were grown on O-methyl substituents as a C1 substrate was determined by 14C radiotracer techniques. O-[methyl-14C]vanillate (4-hydroxy-3-methoxy-benzoate) was used as the labeled C1 substrate. The data showed that for every O-methyl carbon converted to [14C]acetate, two were oxidized to 14CO2. Quantitation of the carbon recovered in the two products, acetate and CO2, indicated that acetate was formed in part by the fixation of unlabeled CO2. The specific activity of 14C in acetate was 70% of that in the O-methyl substrate, suggesting that only one carbon of acetate was derived from the O-methyl group. Thus, it is postulated that the carboxyl carbon of the product acetate is derived from CO2 and the methyl carbon is derived from the O-methyl substituent of vanillate. The metabolism of O-[methyl-14C]vanillate by strain TH-001 can be described as follows: 314CH3OC7H5O3 + CO2 + 4H2O -> 14CH3COOH + 214CO2 + 10H+ + 10e- + 3HOC7H5O3.


FOOTNOTES

* Corresponding author.


Appl Environ Microbiol. 1986 January; 51(1): 84-87
Copyright © 1986, American Society for Microbiology. All Rights Reserved.







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Copyright © 1986 by the American Society for Microbiology. All rights reserved.