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Abstract
Annual Review of Microbiology
Vol. 60: 107-130 (Volume publication date October 2006)
(doi:10.1146/annurev.micro.60.080805.142053)
First published online as a Review in Advance on May 8, 2006
Arsenic and Selenium in Microbial Metabolism*

John F. Stolz,1 ­ Partha Basu,2 ­ Joanne M. Santini,3 and ­ Ronald S. Oremland4­
1Department of Biological Sciences, Duquesne University, Pittsburgh, Pennsylvania 15282; email:
2Department of Chemistry and Biochemistry, Duquesne University, Pittsburgh, Pennsylvania 15282; email:
3Department of Biology, University College London, London WC1E 6BT, United Kingdom; email:
4Water Resources Division, U.S. Geological Survey, Menlo Park, California 94025; email:

Abstract Arsenic and selenium are readily metabolized by prokaryotes, participating in a full range of metabolic functions including assimilation, methylation, detoxification, and anaerobic respiration. Arsenic speciation and mobility is affected by microbes through oxidation/reduction reactions as part of resistance and respiratory processes. A robust arsenic cycle has been demonstrated in diverse environments. Respiratory arsenate reductases, arsenic methyltransferases, and new components in arsenic resistance have been recently described. The requirement for selenium stems primarily from its incorporation into selenocysteine and its function in selenoenzymes. Selenium oxyanions can serve as an electron acceptor in anaerobic respiration, forming distinct nanoparticles of elemental selenium that may be enriched in 76Se. The biogenesis of selenoproteins has been elucidated, and selenium methyltransferases and a respiratory selenate reductase have also been described. This review highlights recent advances in ecology, biochemistry, and molecular biology and provides a prelude to the impact of genomics studies.

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Authors:
John F. Stolz
Partha Basu
Joanne M. Santini
Ronald S. Oremland
Keywords:
selenate respiration
selenocysteine
arsenate reductase
arsenite oxidase
biogeochemical cycles
organoarsenicals

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