4.8 Article

NemA Catalyzes Trivalent Organoarsenical Oxidation and Is Regulated by the Trivalent Organoarsenical-Selective Transcriptional Repressor NemR

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 55, Issue 9, Pages 6485-6494

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.1c00574

Keywords

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Funding

  1. National Key Research and Development Program of China [2016YFD0800702]
  2. National Natural Science Foundation of China [31900078]
  3. China Postdoctoral Science Foundation [2019M662655]
  4. NIH [R35 GM136211, R01 GM55425, R01 ES023779]

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Synthetic aromatic arsenicals have been widely used in agriculture as animal growth enhancers and herbicides. This study identifies the nemRA operon from Enterobacter sp. Z1 and shows that it is involved in trivalent organoarsenical oxidation. The discovery of NemA as a novel trivalent organoarsenical oxidase expands our understanding of the molecular mechanisms of organoarsenical oxidation.
Synthetic aromatic arsenicals such as roxarsone (Rox(V)) and nitarsone (Nit(V)) have been used as animal growth enhancers and herbicides. Microbes contribute to redox cycling between the relatively less toxic pentavalent and highly toxic trivalent arsenicals. In this study, we report the identification of nemRA operon from Enterobacter sp. Z1 and show that it is involved in trivalent organoarsenical oxidation. Expression of nemA is induced by chromate (Cr(VI)), Rox(III), and Nit(III). Heterologous expression of NemA in Escherichia coli confers resistance to Cr(VI), methylarsenite (MAs(III)), Rox(III), and Nit(III). Purified NemA catalyzes simultaneous Cr(VI) reduction and MAs(III)/Rox(III)/Nit(III) oxidation, and oxidation was enhanced in the presence of Cr(VI). The results of electrophoretic mobility shift assays and fluorescence assays demonstrate that the transcriptional repressor, NemR, binds to either Rox(III) or Nit(III). NemR has three conserved cysteine residues, Cys21, Cys106, and Cys116. Mutation of any of the three resulted in loss of response to Rox(III)/Nit(III), indicating that they form an Rox(III)/Nit(III) binding site. These results show that NemA is a novel trivalent organoarsenical oxidase that is regulated by the trivalent organoarsenical-selective repressor NemR. This discovery expands our knowledge of the molecular mechanisms of organoarsenical oxidation and provides a basis for studying the redox coupling of environmental toxic compounds.

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