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 (strp) was mapped upstream of ybxF, and its strength was compared with the strength of the tuf-specific promoter (tufp) located in the fus-tuf intergenic region. The strength of the tufp region to initiate transcription is about 20-fold higher than that of the strp 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 strp (an inhibitory region) and tufp (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.The streptomycin operon (str) belongs among the mostconserved operons in prokaryotic evolution (20,27). The str operon of Escherichia coli, from which most of our knowledge about this operon is derived, is composed of four genes: rpsL (coding for ribosomal protein S12), rpsG (ribosomal protein S7), fus (elongation factor G [EF-G]), and tufA (elongation factor Tu [EF-Tu]). It is transcribed from its main promoter situated upstream of the rpsL gene (43). Besides the main promoter, two additional promoters, located within the fus gene, direct the transcription of the tufA gene (1, 57, 59). Zengel and Lindahl estimated the combined activity of these additional promoters to be about 30% of the activity of the main promoter (58, 59). These promoters, as well as the second copy of the tuf gene (tufB) present in the E. coli chromosome (21), contribute to the increased expression of EF-Tu relative to the expression of other genes of the str operon.Approximately 50 str operons have already been sequenced. However, only a few of them were also characterized functionally by their transcriptional products and transcriptional starts. In our previous work, we cloned and characterized the tuf gene of Bacillus stearothermophilus. A tuf-specific promoter (tufp) was detected in the fus-tuf intergenic region. Based on Northern blot experiments, the ratio between the tuf-specific and the polycistronic transcript was estimated to be at least 10:1 (28).In the present work, we extended our studies to the rest of the str operon of B. stearothermophilus with a special focus on the characterization of the promoters of this operon. As a prerequisite, the complete primary structure of the str operon of B. stearothermophilus was determined, and the main operon promoter (strp) was mapped. By using the chloramphenicol acetyltransferase (CAT) assay technique, the strength of the strp promoter was compared with the strength of the ...