Enzymatic reduction of chromate: comparative studies using sulfate reducing bacteria - Key role of polyheme cytochromes c and hydrogenases

Various sulfate-reducing bacteria of the genera Desulfovibrio and Desulfomicrobium were tested and compared for enzymatic reduction of chromate. Our study demonstrated that the ability to reduce chromate is widespread among sulfate-reducing bacteria. Among them, Desulfomicrobium norvegicum reduced Cr(VI) with the highest reaction rate. This strain grew in the presence of up to 500 muM chromate, but Cr(VI) reduction in the absence of sulfate was not associated with growth. The presence of chromate induced morphological changes and leakage of periplasmic proteins into the medium. The ability of isolated polyheme cytochromes c from sulfate- and sulfur-reducing bacteria to reduce chromate was also analyzed. Tetraheme cytochrome c(3)(M-r. 13,000) from Desulfomicrobium norvegicum showed twice as much activity as either tetraheme cytochrome c(3) from Desulfovibrio vulgaris strain Hildenborough or triheme cytochrome c(7) from Desulfuromonas acetoxidans. Results with cytochromes c(3) and other c-type cytochromes altered by site-directed mutagenesis indicated that negative redox potential hemes are crucial for metal reductase activity. The present study also demonstrated that the (Fe) hydrogenase from sulfate-reducing bacteria could reduce chromate.