Transcriptional analysis of the gene for glutamine synthetase II and two upstream genes in Streptomyces coelicolor A3(2)

The glutamine synthetase IT (GSII, encoded by glnII) activity detectable in crude extracts from Streptomyces coelicolor is low compared to the activity of glutamine synthetase I (GSI, encoded by glnA) and to that of GSII fi om S. viridochromogenes. We have identified and sequenced a 3.9-kb Bg/II-BamHI fragment carrying the glutamine synthetase II gene (glnII) from S. coelicolor. Besides glnII, this region contains four ORFs (orf1-orf4). While homologues of orf1 and orf2 were also found in the glnII region of the S. viridochromogenes chromosome, this was not the case for orf3 and orf4, which encode a putative hydrolase and a transcriptional regulator (Ptr) of the MarR family, respectively. High-resolution S1 nuclease mapping showed that the S. coelicolor glnII gene is expressed from two overlapping promoters. The first comprises a vegetative promoter sequence and the second contains sequence elements that are recognized by E sigma (31). Similar promoter structures were found upstream of the S. viridochromogenes glnII gene. The involvement of ptr in glnII regulation was studied by gel retardation assays. Recombinant Ptr interacted with the upstream region of ptr.. but not with the promoter region of glnII. A ptr gene replacement mutant (S. coelicolor IF) was also constructed. RT-PCR analysis of RNA from wild-type S, coelicolor and the IP mutant demonstrated that 0expression of orf3 depends on Ptr. Thus, the difference in gene organization between S, coelicolor and S. viridochromogenes is not responsible for the difference in GSII activity.