The bacterial RNases J are considered bifunctional RNases possessing both endo-and exonucleolytic activities. We have isolated an RNase J ortholog from Streptomyces coelicolor encoded by the gene sco5745. We overexpressed a decahistidine-tagged version of SCO5745 and purified the overexpressed protein by immobilized metal ion affinity chromatography. We demonstrated the presence of both 5=-to-3= exonucleolytic and endonucleolytic activities on the Bacillus subtilis thrS transcript. Exonucleoytic activity predominated with 5= monophosphorylated thrS, while endonucleolytic activity predominated with 5= triphosphorylated thrS. While sco5745 is the only RNase J allele in S. coelicolor, the gene is not essential. Its disruption resulted in delayed production of the antibiotic actinorhodin, overproduction of undecylprodigiosin, and diminished production of the calcium-dependent antibiotic, in comparison with the parental strain.T he decay of mRNA and the concomitant regulation of gene expression at this level are controlled by a number of key RNases present in a variety of combinations in both Gram-negative and Gram-positive bacteria. There is growing appreciation of how evolutionarily distant bacteria functionally combine quite different sets of proteins in the regulation of RNA metabolism (1, 2). RNase J was the first of two bacterial RNases discovered to possess both exo-and endonucleolytic activities. RNase BN acts as a 3=-to-5= distributive exonuclease releasing mononucleotides and producing a ladder of digestion products. Cleaving endonucleolytically, it produces short 3=-end fragments. While active on single-stranded substrates, RNase BN prefers duplexed substrates and is inhibited by the presence of a 3=-end phosphoryl group and 3=-CCA sequence (3).Originally characterized by two alleles in Bacillus subtilis (4), RNase J is widely distributed in other Gram-positive species as a single allele, as in Mycobacterium smegmatis (5), and as two alleles in Streptococcus pyogenes (6). RNases J have also been characterized in the Gram-negative bacterium Sinorhizobium (7), in the hyperthermophilic archaea Pyrococcus abyssi and Thermococcus kodakaraensis (8), and in plant chloroplasts (9). B. subtilis expresses two paralogous proteins, RNase J1 and J2. The two proteins possess endo-and exonuclease activities in vitro but are not equally active. Recently, it has been argued that the major function of RNase J1 is as an exonuclease, and no specific function has been assigned to RNase J2. However, the two proteins form a heterotetramer in vivo that cleaves a model substrate at a different site than the J1 homodimer (10). The single-stranded exonuclease activity of RNases J appears to be strongly dependent upon the phosphorylation state of the 5= end of transcripts, usually showing a distinct preference for the monophosphorylated state (4, 9, 11, 12).Streptomycetes are Gram-positive actinomycetes noted for their production of antibiotics, antifungals, and chemotherapeutic drugs (13). Streptomyces coelicolor is a model for the ...