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Journal of Bacteriology, October 2005, p. 6991-6997, Vol. 187, No. 20
0021-9193/05/$08.00+0     doi:10.1128/JB.187.20.6991-6997.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Novel Pathway for Arsenic Detoxification in the Legume Symbiont Sinorhizobium meliloti

Department of Biochemistry and Molecular Biology, School of Medicine, Wayne State University, Detroit, Michigan 48201,¹ Department of Biology, McMaster University, Hamilton, Ontario L8S 4K1, Canada²

Received 12 May 2005/ Accepted 27 July 2005

We report a novel pathway for arsenic detoxification in the legume symbiont Sinorhizobium meliloti. Although a majority of ars operons consist of three genes, arsR (transcriptional regulator), arsB [As(OH)₃/H⁺ antiporter], and arsC (arsenate reductase), the S. meliloti ars operon includes an aquaglyceroporin (aqpS) in place of arsB. The presence of AqpS in an arsenic resistance operon is interesting, since aquaglyceroporin channels have previously been shown to adventitiously facilitate uptake of arsenite into cells, rendering them sensitive to arsenite. To understand the role of aqpS in arsenic resistance, S. meliloti aqpS and arsC were disrupted individually. Disruption of aqpS resulted in increased tolerance to arsenite but not arsenate, while cells with an arsC disruption showed selective sensitivity to arsenate. The results of transport experiments in intact cells suggest that AqpS is the only protein of the S. meliloti ars operon that facilitates transport of arsenite. Coexpression of S. meliloti aqpS and arsC in a strain of E. coli lacking the ars operon complemented arsenate but not arsenite sensitivity. These results imply that, when S. meliloti is exposed to environmental arsenate, arsenate enters the cell through phosphate transport systems and is reduced to arsenite by ArsC. Internally generated arsenite flows out of the cell by downhill movement through AqpS. Thus, AqpS confers arsenate resistance together with ArsC-catalyzed reduction. This is the first report of an aquaglyceroporin with a physiological function in arsenic resistance.

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