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J. Bacteriol., 02 1996, 638-646, Vol 178, No. 3
P Choi, L Wang, CD Archer and T Elliott
In Salmonella typhimurium and Escherichia coli, the hemA gene encodes the
enzyme glutamyl-tRNA reductase, which catalyzes the first committed step in
the heme biosynthetic pathway. It has recently been reported that a lac
operon fusion to the hemA promoter of E. coli is induced 20- fold after
starvation for heme. Induction was dependent on the transcriptional
regulator ArcA, with a second transcriptional regulator, FNR, playing a
negative role specifically under anaerobic conditions (S. Darie and R. P.
Gunsalus, J. Bacteriol. 176:5270-5276, 1994). We have investigated the
generality of this effect by examining the response to heme starvation of a
number of lac operon fusions to the hemA promoters of both E. coli and S.
typhimurium. We confirmed that such fusions are induced during starvation
of a hemA auxotroph, but the level of induction observed was maximally
sixfold and for S. typhimurium fusions it was only two- to fourfold.
Sequences required for high-level expression of hemA lie within 129 bp
upstream of the major (P1) promoter transcriptional start site. Mutants
defective in the P1 promoter had greatly reduced hemA-lac expression both
in the presence and in the absence of ALA. Mutations in arcA had no effect
on hemA-lac expression in E. coli during normal growth, although the
increase in expression during starvation for ALA was half that seen in an
arcA+ strain. Overexpression of the arcA gene had no effect on hemA- lac
expression. Primer extension analysis showed that RNA 5' ends mapping to
the hemA P1 and P2 promoters were not expressed at significantly higher
levels in induced cultures. These results differ from those previously
reported.
Copyright © 1996, American Society for Microbiology
Transcription of the glutamyl-tRNA reductase (hemA) gene in Salmonella typhimurium and Escherichia coli: role of the hemA P1 promoter and the arcA gene product
Department of Microbiology and Immunology, West Virginia University, Health Sciences Center, Morgantown 26506, USA.
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