PMID:15250887
| Citation |
Ackerley, DF, Gonzalez, CF, Keyhan, M, Blake, R 2nd and Matin, A (2004) Mechanism of chromate reduction by the Escherichia coli protein, NfsA, and the role of different chromate reductases in minimizing oxidative stress during chromate reduction. Environ. Microbiol. 6:851-60 |
|---|---|
| Abstract |
Chromate [Cr(VI)] is a serious environmental pollutant, which is amenable to bacterial bioremediation. NfsA, the major oxygen-insensitive nitroreductase of Escherichia coli, is a flavoprotein that is able to reduce chromate to less soluble and less toxic Cr(III). We show that this process involves single-electron transfer, giving rise to a flavin semiquinone form of NfsA and Cr(V) as intermediates, which redox cycle, generating more reactive oxygen species (ROS) than a divalent chromate reducer, YieF. However, NfsA generates less ROS than a known one-electron chromate reducer, lipoyl dehydrogenase (LpDH), suggesting that NfsA employs a mixture of uni- and di-valent electron transfer steps. The presence of YieF, ChrR (another chromate reductase we previously characterized), or NfsA in an LpDH-catalysed chromate reduction reaction decreased ROS generation by c. 65, 40, or 20%, respectively, suggesting that these enzymes can pre-empt ROS generation by LpDH. We previously showed that ChrR protects Pseudomonas putida against chromate toxicity; here we show that NfsA or YieF overproduction can also increase the tolerance of E. coli to this compound. |
| Links |
PubMed Online version:10.1111/j.1462-2920.2004.00639.x |
| Keywords |
Amino Acid Sequence; Chromates/metabolism; Chromates/toxicity; Dihydrolipoamide Dehydrogenase/metabolism; Drug Resistance, Neoplasm; Electron Transport; Electron-Transferring Flavoproteins/metabolism; Escherichia coli/drug effects; Escherichia coli/metabolism; Escherichia coli Proteins/genetics; Escherichia coli Proteins/metabolism; Gene Dosage; Molecular Sequence Data; Nitroreductases/genetics; Nitroreductases/metabolism; Oxidation-Reduction; Oxidative Stress; Oxidoreductases/physiology; Pseudomonas/genetics; Reactive Oxygen Species/analysis; Sequence Homology, Amino Acid |
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