The genetic basis for bacterial mercury methylation

Jerry M. Parks, Alexander Johs, Mircea Podar, Romain Bridou, Richard A. Hurt, Steven D. Smith, Stephen J. Tomanicek, Yun Qian, Steven D. Brown, Craig C. Brandt, Anthony V. Palumbo, Jeremy C. Smith, Judy D. Wall, Dwayne A. Elias, Liyuan Liang

Research output: Contribution to journalArticlepeer-review

773 Scopus citations

Abstract

Methylmercury is a potent neurotoxin produced in natural environments from inorganic mercury by anaerobic bacteria. However, until now the genes and proteins involved have remained unidentified. Here, we report a two-gene cluster, hgcA and hgcB, required for mercury methylation by Desulfovibrio desulfuricans ND132 and Geobacter sulfurreducens PCA. In either bacterium, deletion of hgcA, hgcB , or both genes abolishes mercury methylation. The genes encode a putative corrinoid protein, HgcA, and a 2[4Fe-4S] ferredoxin, HgcB, consistent with roles as a methyl carrier and an electron donor required for corrinoid cofactor reduction, respectively. Among bacteria and archaea with sequenced genomes, gene orthologs are present in confirmed methylators but absent in nonmethylators, suggesting a common mercury methylation pathway in all methylating bacteria and archaea sequenced to date.

Original languageEnglish
Pages (from-to)1332-1335
Number of pages4
JournalScience
Volume339
Issue number6125
DOIs
StatePublished - Mar 15 2013

Fingerprint

Dive into the research topics of 'The genetic basis for bacterial mercury methylation'. Together they form a unique fingerprint.

Cite this