β-galactosidase activity conferred by the pUWM827 fusion increased under iron-sufficient/rich conditions in the fur mutant as compared to the wild-type strain, suggesting that inactivation of fur results in derepression of P dbadsbI . In contrast, β-galactosidase activities of the pUWM803 and pUWM864 fusions increased under iron starvation in the fur mutant compared to the wild-type strain. This indicates that low level of iron leads to Fur-mediated repression of the P dsbA2dsbBastA and P dsbA1 promoters, Tozasertib purchase since repression was abolished in the fur mutated strain. C. jejuni 480 strain containing pUWM471, which harbors cjaA gene promoter fused to a promotorless lacZ gene, was

employed as a control in all experiments analyzing the influence of Fur and iron on dsb gene expression. There were no significant differences in β-galactosidase activity between wild type cells harbouring pUWM471 grown at various iron concentrations as well as between wt and fur mutated cells containing pUWM471. In every case high β-galactosidase levels (about 2000 Miller units) were observed, which is consistent with previously published data that

ranked the cjaA promoter as one of the the strongest Campylobacter spp. promoters so far described [39]. Inspection of the nucleotide sequences Birinapant molecular weight located Selleckchem GSK1210151A upstream of the dba translation initiation codon did not reveal the presence of an exact C. jejuni Fur-binding site sequence motif [40]. So far, a potential Fur binding site for promoters positively regulated by iron concentration in a Fur- dependent manner has not been determined. Therefore, we used EMSA to gain insight into the mechanism by which P dbadsbI , P dsbA2dsbBastA and P dsbA1 are regulated by Fur. To achieve

this goal, various primers were designed to amplify a 174 – 299 bp DNA fragment upstream from the translational start site of each tested operon. The promoter region of the chuA gene, which contains the Fur-binding motif and is strongly repressed by iron-complexed Fur, the was used as a control [6, 40]. Mn2+ ions were used in the EMSA in place of Fe2+ due to their greater redox stability. It was demonstrated that the Fur-His6 was able to bind in vitro to the DNA region upstream of the dba-dsbI operon only when the regulatory protein was complexed with Mn2+, which indicated, in accordance with previously presented data, that this operon is repressed by the iron-complexed form of Fur (Figure 3E). This promoter region interacts with Fur complexed with Mn2+ as much as the chuA promoter (Figure 3G). In contrast, the upstream DNA region of the dsbA1 gene did not bind Fur, regardless of the presence of Mn2+ in the reaction buffer. This suggested an indirect method of regulation (Figure 3, panel C and D). In the case of the dsbA2-dsbB-astA promoter region, Fur protein bound DNA in the absence of Mn2+ acted as a repressor (Figure 3B), supporting the results obtained in the β-galactosidase assays.