Since the mpt operon is σ54-regulated, we MI-503 in vivo examined if other σ54-controlled genes were affected in the mutants. By in silico analysis of the genome sequence of E. faecalis V583 using the sigma-54 promoter specific consensus sequence of B. subtilis YTGGCACNNNNNTTGCW [38], 10 putative σ54-dependent promoters selleck chemicals were identified. Four of them are preceded by a gene encoding a σ54-dependent
activator, and downstream genes encoding PTS enzyme II. Only the mpt operon showed reduced expression, while up-regulation only was observed for mphD localized downstream of EF1955 encoding a LevR-like σ54-dependent activator. Involvement of catabolite-responsive elements (cre) The large number of up-regulated catabolic genes in the mutants suggests the involvement of a global regulator. In Firmicutes carbon catabolite repression (CCR) is mediated via binding of the catabolite control protein A (CcpA) to operators known as catabolite-responsive elements cre [39]. By searching the E.
faecalis V583 genome using the cre query consensus sequence WTGNAANCGNWNNCW developed for B. subtilis [40], we found 34 intergenic putative catabolite-responsive elements, and 21 of them were in the promoter regions of operons showing significant CYT387 mouse increased transcription in the mutants (see Additional file 1). Another 42 of the promoter regions of differentially expressed genes contained sequences with one mismatch to the B. subtilis cre-consensus. We propose that these sequences represent cre-sites of E. faecalis (see Additional file
2). Their sequences were aligned and had the consensus sequence WTGWAARCGYWWWCW. Many of the differentially expressed genes contained this sequence in their coding regions, and two were located ifenprodil in the intergenic regions downstream the down-regulated genes EF0635 and EF1046 (see Additional file 1). As shown in Additional file 1, a large majority of the differentially expressed genes are associated with putative cre-sites, and seven of them possibly regulate divergent expression. Many of the up-regulated genes located downstream of putative cre-sites encode enzymes involved in the use of alternative energy and carbon sources. Among them, genes encoding enzymes involved in citrate transport and catabolism (EF3314 to 3328) had the greatest increase in expression, up to sixty-fourfold in the mutants. A cre-site was found in the intergenic region between the two divergent cit operons. The arc operon, preceded by a cre-site encodes the energy yielding enzymes by arginine consumption, was also up-regulated in the mutants.