1). All the defects were complemented by the presence of a copy of rho in a plasmid (Italiani et al., 2002). These results suggest a generalized defect in the oxidative stress response because the rho mutant strain SP3710 shows increased sensitivity IWR-1 clinical trial to H2O2, organic hydroperoxides and superoxide. Because the rho mutant showed increased sensitivity to several classes of oxidants, we considered

that it could be permanently experiencing oxidative stress, rendering it more difficult to tolerate the stress of exogenous oxidants. To test this hypothesis, exponential-phase cells were incubated with dihydrorhodamine 123, a dye showing an oxidation-dependent increase in fluorescence. These cells were analyzed by fluorescence microscopy (Fig. 2, even-numbered panels) and light microscopy (odd-numbered panels) to determine the fraction of cells with visible fluorescence. Strain NA1000 shows no fluorescence in the absence of exogenous H2O2 (Fig. 2, panel 2) compared with fluorescence

in all cells after exposure to 5 mM H2O2 (Fig. 2, panel 4). In contrast, SP3710 cells show fluorescence even in the absence of exogenous H2O2 (Fig. 2, selleck chemical panel 6), indicating that they are permanently in an oxidative state. Complementation of strain SP3710 with wild-type rho in trans restores fluorescence to the level of untreated strain NA1000 (compare panels 8 and 2 in Fig. 2). Because the rho mutant is permanently Acyl CoA dehydrogenase under oxidative stress, we next determined whether expression of antioxidant enzymes was negatively

affected in this strain. Endogenous oxidative stress during aerobic growth may arise from leakage of electrons from the respiratory chain and reaction with molecular oxygen as well as from other sources (Seaver & Imlay, 2004). As an obligate aerobe, C. crescentus has a panel of antioxidant enzymes for defense against endogenous oxidative stress. The response to organic hydroperoxides is likely to be mediated largely by alkylhydroperoxide reductase (Ahp), composed of two subunits: AhpC, which donates electrons to peroxides, and AhpF, a flavoprotein AhpC-reductase (Poole, 2005). Semi-quantitative RT-PCR showed that the levels of ahpC mRNA were substantially higher in the exponential phase than in the stationary phase (Fig. 3a), but no obvious difference was evident between ahpC levels in SP3710 and NA1000. These results suggest that increased sensitivity to tert-butyl hydroperoxide in SP3710 (Table 1) is unlikely to be attributable to decreased transcription of ahpC. Activity staining in nondenaturing acrylamide gels was used to compare the levels of the SODs in NA1000 and the SP3710 mutant. When activity gels are performed on whole-cell extracts of NA1000, two SOD bands appear, attributed to CuZnSOD and FeSOD, and no differences were observed between NA1000 and SP3710 strains in either the exponential or the stationary phase for these activities (Fig. 3b).