The planktonic cells were removed and stored, the tubes were washed three times with normal saline and biofilm-associated cells were shifted into suspension in 0.5 mL normal saline by vortexing in the presence of 1-mm-diameter borosilicate glass beads (Sigma). β-Galactosidase activity SAHA HDAC mw was measured as described previously (Miller, 1971) using the substrate o-nitrophenyl-β-d-galctotopyranoside. Specific
activities are given in Miller units [1000 × OD420 nm/tv× OD600 nm)] where t is the reaction time and v is the volume of enzyme extract per reaction. Vibrio cholerae strains were grown for 16 h in LB medium at 37 °C. The culture was then diluted to 106–107 cells mL−1 in fresh low-phosphate EZ-rich defined medium containing 1.2 M NaCl, 0.5 mM hydrogen peroxide, pH 4.5, or lacking a carbon source. Cultures were incubated at 37 °C with shaking (250 r.p.m.), and samples were taken at different time points to determine viability by dilution plating on LB agar plates. Repression of HapR requires the regulator LuxO to be phosphorylated (Lenz et al., 2004). Therefore, we reasoned that phosphate-limited conditions might increase the expression of HapR by diminishing the amount of high-energy phosphate required to activate LuxO. To test this hypothesis, we constructed the HapR reporter strain SZS007 to monitor the production of active HapR protein
in high- and low-phosphate media. To this end, we replaced the V. cholerae native lacZ promoter in the C7258 chromosome by the HapR-regulated V. harveyi H 89 chemical structure luxC promoter. Expression of β-galactosidase activity by the wild-type strain containing the luxC–lacZ transcriptional fusion followed the typical U-shaped cell density-dependent pattern (Fig. 1a). No β-galactosidase activity could be detected in the isogenic hapR deletion mutant SZS009 after growth to the highest cell density in LB medium (Fig. 1a). We next used this reporter strain to examine
the effect of phosphate limitation on HapR expression. The reporter strain was grown to OD600 nm 1 in high-phosphate EZ-rich defined medium, the cells were centrifuged and reconstituted in 1 vol. of the same medium containing 0.132 mM and no phosphate. As shown Selleck Atezolizumab in Fig. 1b, higher β-galactosidase activities were detected after incubation under phosphate-limiting conditions. To further document the effect of phosphate limitation on HapR expression, we took advantage of the strain AJB26 derivative of V. cholerae C6709ΔlacZ, which contains a chromosomally integrated hapR–lacZ transcriptional fusion previously shown to recapitulate the cell density-dependent regulation of HapR (Silva & Benitez, 2004). This strain provided an opportunity to test the effect of phosphate limitation on HapR expression in a different strain with a different indicator system.