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Purine metabolism by Methanococcus vannielii

Journal Article · · Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:6991243
During studies of biosynthesis of novel cofactors in Methanococcus vannielii, it was discovered that guanine and xanthine are degraded by extracts of this organism. Using labeled substrates it was shown that uric acid, guanine, and hypoxanthine are converted to xanthine, which is then degraded in a manner similar to that described by Rabinowitz and Barker for clostridia. Extracts of M. vannielii convert the 2-, 6-, and 8-carbon atoms of xanthine to CO/sub 2/. It appears that the 8-carbon is initially lost as formate, which is then oxidized to CO/sub 2/ by the endogenous formate dehydrogenase. Enzyme preparations exposed to oxygen failed to convert (/sup 14/C)xanthine or (/sup 14/C)guanine either to CO/sub 2/ or to a form not adsorbed to charcoal. This oxygen inhibition could be reversed by treatment with dithiothreitol. Extracts exposed to oxygen apparently fail to carry out the initial step in xanthine degradation. The overall reaction for the degradation of guanine or xanthine is inhibited by EDTA and this inhibition is reversed by supplements of Mn/sup 2 +/ or Fe/sup 2 +/. Based on these studies, it was shown that uric acid, guanine, hypoxanthine, or xanthine could serve as sole nitrogen source for growth of the organism.
Research Organization:
National Institutes of Health, Bethesda, MD
OSTI ID:
6991243
Report Number(s):
CONF-8606151-
Journal Information:
Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States), Journal Name: Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States) Vol. 45:6; ISSN FEPRA
Country of Publication:
United States
Language:
English