Abstract
Biological reduction of carcinogenic chromate has been extensively studied in eukaryotic cells partly because the reduction produces stable chromium(III)-DNA adducts, which are mutagenic. Microbial reduction of chromate has been studied for bio-remediation purposes, but little is known about the reduction mechanism. In eukaryotic cells chromate is mainly reduced non-enzymatically by ascorbate, which is usually absent in bacterial cells. We have characterized the reduction of chromate by a flavin reductase (Fre) from Escherichia coli with flavins. The Fre-flavin system rapidly reduced chromate, whereas chemical reduction by NADH and glutathione was very slow. Thus, enzymatic chromate reduction is likely the dominant mechanism in bacterial cells. Furthermore, the end-product was a soluble and stable Cr(III)-NAD+ complex, instead of Cr(III) precipitate. Since intracellularly generated Cr(III) forms adducts with DNA, protein, glutathione, and ascorbate in eukaryotic cells, we suggest that the produced Cr(III) is primarily complexed to NAD+, DNA, and other cellular components inside bacteria. © 2002 Elsevier Science Ltd. All rights reserved.
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Puzon, G. J., Petersen, J. N., Roberts, A. G., Kramer, D. M., & Xun, L. (2002). A bacterial flavin reductase system reduces chromate to a soluble chromium(III)-NAD+ complex. Biochemical and Biophysical Research Communications, 294(1), 76–81. https://doi.org/10.1016/S0006-291X(02)00438-2
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