Cloning and Characterization of the str Operon and Elongation Factor Tu Expression in Bacillus stearothermophilus

Abstract

ABSTRACT The complete primary structure of the str operon of Bacillus stearothermophilus was determined. It was established that the operon is a five-gene transcriptional unit: 5′- ybxF (unknown function; homology to eukaryotic ribosomal protein L30)- rpsL (S12)- rpsG (S7)- fus (elongation factor G [EF-G])- tuf (elongation factor Tu [EF-Tu])-3′. The main operon promoter ( str p) was mapped upstream of ybxF , and its strength was compared with the strength of the tuf -specific promoter ( tuf p) located in the fus-tuf intergenic region. The strength of the tuf p region to initiate transcription is about 20-fold higher than that of the str p region, as determined in chloramphenicol acetyltransferase assays. Deletion mapping experiments revealed that the different strengths of the promoters are the consequence of a combined effect of oppositely acting cis elements, identified upstream of str p (an inhibitory region) and tuf p (a stimulatory A/T-rich block). Our results suggest that the oppositely adjusted core promoters significantly contribute to the differential expression of the str operon genes, as monitored by the expression of EF-Tu and EF-G.