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Journal of Bacteriology, July 2008, p. 4596-4602, Vol. 190, No. 13
0021-9193/08/$08.00+0 doi:10.1128/JB.00262-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Department of Bacteriology, University of Wisconsin, Madison, Madison, Wisconsin 53706
Received 20 February 2008/ Accepted 13 April 2008
Mutants of Salmonella enterica lacking apbC have nutritional and biochemical properties indicative of defects in [Fe-S] cluster metabolism. Here we show that apbC is required for S. enterica to use tricarballylate as a carbon and energy source. Tricarballylate catabolism requires three gene products, TcuA, TcuB, and TcuC. Of relevance to this work is the TcuB protein, which has two [4Fe-4S] clusters required for function, making it a logical target for the apbC effect. TcuB activity was 100-fold lower in an apbC mutant than in the isogenic apbC+ strain. Genetic data show that derepression of the iscRSUA-hscAB-fdx-orf3 operon or overexpression of iscU from a plasmid compensates for the lack of ApbC during growth on tricarballylate. The studies described herein provide evidence that the scaffold protein IscU has a functional overlap with ApbC and that ApbC function is involved in the synthesis of active TcuB.
Published ahead of print on 25 April 2008.
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