Thus, horizontal acquisition of regulatory proteins can have a significant impact on ancestral gene expression often by interacting

Selleck AZD5582 with other regulatory pathways. Conclusions We have shown that the non-motile phenotype of Δhha ΔydgT requires the loss of both Hha and YdgT and that this phenotype is partially mediated through PefI-SrgD. These data contribute to our understanding of Hha-and YdgT-dependent flagellar biosynthesis regulation and demonstrate the integration of the horizontally acquired regulators PefI-SrgD into the flagellar biosynthesis network. Methods Bacterial Strains and Mutant Construction Bacteria were propagated in Luria-Bertani (LB) broth at 37°C with aeration unless otherwise PI3K Inhibitor Library chemical structure indicated. Marked, in-frame deletions of clpXP

and pefI-srgD were made in Salmonella enterica serovar Typhimurium SL1344 using the λ Red Recombinase method [38]. Generation of Δhha ΔydgT was described previously [15] and this strain was used to generate mutants incorporating the pefI-srgD deletion using the primers pefI-srgDF: GTG ATA CTT ATC CGG CCT CCG GTC CGC ATT CCA GGC CGG CCA TAT GAA TAT CCT CCT TAG and pefI-srgDR ATT CCG GTT TAT GAG TGA ATC CAT TGT TAC AAA AAT TAT TGT GTA GGC TGG AGC TGC TTC. Soft Agar Motility Assay Two μl of overnight culture was inoculated into 0.25% LB Agar motility plates with antibiotic and incubated at 37°C for 6 h. Immunoblotting Wild type and mutant strains 4EGI-1 in vitro see more were cultured until the optical density at 600 nm (OD600) reached ~ 0.4-0.6. Whole cell lysates were collected and probed using anti-FlhC (1:5000), anti-FlhD (1:2500) and anti-DnaK (1:5000, Stressgen) antibodies. DnaK served as a loading

control. Transmission Electron Microscopy Flagella were negatively stained using two different methods. In the first method, cells were cultured for 3-6 h. A carbon-stabilized Formvar support on 200-mesh copper TEM grid was floated for 30 seconds on a drop of culture, washed three times with water and stained for 10 seconds using 0.1% uranyl acetate. The second method involved staining copper grid-immobilized cells for 60 seconds with 2% phosphotungstic acid. Images were obtained using a JEOL-1200EX transmission electron microscope at the McMaster University Electron Microscopy Facility. For quantification, overnight cultures were diluted 1:50 or 1:100 in LB media with antibiotic and grown for at least 3 hours under static conditions. Flagella were stained as described above and quantified for at least 100 cells. Transcriptional Reporter Assays Wild type cells and the various mutants under study were transformed with the plasmid-based green fluorescent protein (GFP) reporter constructs pP flhD -GFP, pP fliA -GFP, pP fliC -GFP and pP less -GFP published previously [39].