Affiliation:
1. Department of Biochemistry and Microbiology, Rutgers University, New Brunswick, New Jersey 08903
Abstract
Substrate-electron acceptor combinations and specific metabolic inhibitors were applied to anoxic saltmarsh sediment spiked with mercuric ions (Hg
2+
) in an effort to identify, by a direct approach, the microorganisms responsible for the synthesis of hazardous monomethylmercury. 2-Bromoethane sulfonate (30 mM), a specific inhibitor of methanogens, increased monomethylmercury synthesis, whereas sodium molybdate (20 mM), a specific inhibitor of sulfate reducers, decreased Hg
2+
methylation by more than 95%. Anaerobic enrichment and isolation procedures yielded a
Desulfovibrio desulfuricans
culture that vigorously methylated Hg
2+
in culture solution and also in samples of presterilized sediment. The Hg
2+
methylation activity of sulfate reducers is fully expressed only when sulfate is limiting and fermentable organic substrates are available. To date, sulfate reducers have not been suspected of Hg
2+
methylation. Identification of these bacteria as the principal methylators of Hg
2+
in anoxic sediments raises questions about the environmental relevance of previous pure culture-based methylation work.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
986 articles.
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