Methylmercury uptake and degradation by methanotrophs.

Abstract

Methylmercury (CH₃Hg⁺) is a potent neurotoxin produced by certain anaerobic microorganisms in natural environments. Although numerous studies have characterized the basis of mercury (Hg) methylation, no studies have examined CH₃Hg⁺ degradation by methanotrophs, despite their ubiquitous presence in the environment. We report that some methanotrophs, such as <i>Methylosinus trichosporium</i> OB3b, can take up and degrade CH₃Hg⁺ rapidly, whereas others, such as <i>Methylococcus capsulatus</i> Bath, can take up but not degrade CH₃Hg⁺. Demethylation by <i>M. trichosporium</i> OB3b increases with increasing CH₃Hg⁺ concentrations but was abolished in mutants deficient in the synthesis of methanobactin, a metal-binding compound used by some methanotrophs, such as <i>M. trichosporium</i> OB3b. Furthermore, addition of methanol (>5 mM) as a competing one-carbon (C1) substrate inhibits demethylation, suggesting that CH₃Hg⁺ degradation by methanotrophs may involve an initial bonding of CH₃Hg⁺ by methanobactin followed by cleavage of the C-Hg bond in CH₃Hg⁺ by the methanol dehydrogenase. This new demethylation pathway by methanotrophs indicates possible broader involvement of C1-metabolizing aerobes in the degradation and cycling of toxic CH₃Hg⁺ in the environment.