Sulfate-Reducing Bacteria: Principal Methylators of Mercury in Anoxic Estuarine Sediment

Author:

Compeau G. C.1,Bartha R.1

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

Reference21 articles.

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4. Methylation and demethylation of mercury under controlled redox, pH, and salinity conditions;Compeau G.;Appl. Environ. Microbiol.,1984

5. Effects of sea salt anions on the formation and stability of methylmercury;Compeau G. C.;Bull. Environ. Contam. Toxicol.,1983

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