Demethylation of Methylmercury in Bird, Fish, and Earthworm
Author(s) -
Alain Manceau,
JeanPaul Bourdineaud,
Ricardo Bezerra de Oliveira,
Sandra Layse Ferreira Sarrazin,
David P. Krabbenhoft,
Collin A. EaglesSmith,
Joshua T. Ackerman,
A. Robin Stewart,
Christian Ward-Deitrich,
M. Estela del Castillo Busto,
Heidi GoenagaInfante,
Aude Wack,
Marius Retegan,
Blanka Detlefs,
Pieter Glatzel,
Paco Bustamante,
Kathryn L. Nagy,
Brett A. Poulin
Publication year - 2021
Publication title -
environmental science and technology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.851
H-Index - 397
eISSN - 1520-5851
pISSN - 0013-936X
DOI - 10.1021/acs.est.0c04948
Subject(s) - methylmercury , mercury (programming language) , environmental chemistry , chemistry , demethylation , inductively coupled plasma mass spectrometry , selenium , mass spectrometry , biochemistry , bioaccumulation , chromatography , organic chemistry , gene expression , computer science , dna methylation , gene , programming language
Toxicity of methylmercury (MeHg) to wildlife and humans results from its binding to cysteine residues of proteins, forming MeHg-cysteinate (MeHgCys) complexes that hinder biological functions. MeHgCys complexes can be detoxified in vivo , yet how this occurs is unknown. We report that MeHgCys complexes are transformed into selenocysteinate [Hg(Sec) 4 ] complexes in multiple animals from two phyla (a waterbird, freshwater fish, and earthworms) sampled in different geographical areas and contaminated by different Hg sources. In addition, high energy-resolution X-ray absorption spectroscopy (HR-XANES) and chromatography-inductively coupled plasma mass spectrometry of the waterbird liver support the binding of Hg(Sec) 4 o selenoprotein P and biomineralization of Hg(Sec) 4 o chemically inert nanoparticulate mercury selenide (HgSe). The results provide a foundation for understanding mercury detoxification in higher organisms and suggest that the identified MeHgCys to Hg(Sec) 4 demethylation pathway is common in nature.
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