A strategy was devised to identify Escherichia coli genes subject to c
oregulation by purR. From a data base search, similarities to the pur
regulon cis-acting control site were found in 26 E. coli genes. Of fiv
e genes examined in which the putative pur operator is upstream of the
coding sequence, glnB, prsA, and speA bound purified purine repressor
in vitro. Binding of the repressor to a pur operator in these genes w
as dependent upon a corepressor. The pur operator in glnB is located b
etween two major transcription start sites that were located by primer
extension mapping. The effect of purR on expression of glnB, prsA, an
d speA was examined by using a lacZ reporter. The results indicated tw
o- to threefold repression of these genes by purR. Coregulation by pur
R provides evidence that expands the pur regulon to include glnB, prsA
, and speA. These genes have functions related to nucleotide metabolis
m.