
Microbial arsenic: from geocycles to genes and enzymes
Author(s) -
Mukhopadhyay Rita,
Rosen Barry P,
Phung Le T,
Silver Simon
Publication year - 2002
Publication title -
fems microbiology reviews
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.91
H-Index - 212
eISSN - 1574-6976
pISSN - 0168-6445
DOI - 10.1111/j.1574-6976.2002.tb00617.x
Subject(s) - arsenate , arsenite , arsenic , biology , archaea , operon , biochemistry , enzyme , microbial metabolism , bacteria , gene , yeast , genetics , chemistry , organic chemistry , escherichia coli
Arsenic compounds have been abundant at near toxic levels in the environment since the origin of life. In response, microbes have evolved mechanisms for arsenic resistance and enzymes that oxidize As(III) to As(V) or reduce As(V) to As(III). Formation and degradation of organoarsenicals, for example methylarsenic compounds, occur. There is a global arsenic geocycle, where microbial metabolism and mobilization (or immobilization) are important processes. Recent progress in studies of the ars operon (conferring resistance to As(III) and As(V)) in many bacterial types (and related systems in Archaea and yeast) and new understanding of arsenite oxidation and arsenate reduction by respiratory‐chain‐linked enzyme complexes has been substantial. The DNA sequencing and protein crystal structures have established the convergent evolution of three classes of arsenate reductases (that is classes of arsenate reductases are not of common evolutionary origin). Proposed reaction mechanisms in each case involve three cysteine thiols and S–As bond intermediates, so convergent evolution to similar mechanisms has taken place.