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. 1990 Jul;172(7):3799–3803. doi: 10.1128/jb.172.7.3799-3803.1990

Regulation of the Escherichia coli glyA gene by the purR gene product.

J G Steiert 1, R J Rolfes 1, H Zalkin 1, G V Stauffer 1
PMCID: PMC213358  PMID: 2113912

Abstract

The purine regulon repressor protein, PurR, was shown to be a purine component involved in glyA regulation in Escherichia coli. Expression of glyA, encoding serine hydroxymethyltransferase activity, was elevated in a purR mutant compared with a wild-type strain. When the purR mutant was transformed with a plasmid carrying the purR gene, the serine hydroxymethyltransferase levels returned to the wild-type level. The PurR protein bound specifically to a DNA fragment carrying the glyA control region, as determined by gel retardation. In a DNase I protection assay, a 24-base-pair region was protected from DNase I digestion by PurR. The glyA operator sequence for PurR binding is similar to that reported for several pur regulon genes.

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Selected References

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