3 mM diaminopimelic HM781-36B supplier acid (DAP) and transferred to W3-18-1 by conjugation [21]. Integration of mutagenesis plasmids into the chromosome was selected by gentamycin resistance and confirmed by PCR amplification. Then transconjugants were grown in LB broth free of NaCl and plated on the LB plates supplemented with 10% of sucrose. Gentamycin-sensitive and sucrose-resistant colonies were screened by PCR to detect gene deletion, which was subsequently verified by DNA sequencing of the mutated region, and the deletion

strain was designated as JZ2622(ΔundA), JZ2623(ΔmtrC) and JZ26223(ΔmtrC-undA). MtrC, UndA and MtrC-UndA complementation For complementation, a 2.5-kb DNA fragment containing mtrC and its native promoter, a 2.9-kb DNA fragment containing undA and its native promoter, AICAR research buy a 5.3-kb DNA fragment containing mtrC and undA and their native promoters were generated by PCR with W3-18-1 genomic DNA as the template (primers are listed in Additional file 1: Table S2). These fragments were digested with BamHI and ligated to BamHI-digested pBBR1MCS-2 to form pBBR1MCS-2-sputw2623,

pBBR1MCS-2-sputw2622, and pBBR1MCS-2-sputw26223. Subsequently, plasmids were electroporated into WM3064 and introduced into the corresponding mutant by conjugation. Kanamycin-resistant colonies of the conjugants were selected for further examination. The presence of plasmids in the complementing strains Depsipeptide order was confirmed by plasmid purification and restriction enzyme digestion. Physiological and iron reduction measurement Three replicates of strains were tested in all physiological experiments, which allows for two-way t test to determine the significance, and non-parametric dissimilarity test using adonis algorithm [22, 23]. All physiological experiments were carried out under Savolitinib anaerobic condition with sodium lactate (20 mM, pH 7.0) as the electron donor, and ferric citrate (20 mM), α-FeO(OH) (20 mM), β-FeO(OH) (20 mM) or Fe2O3 (20 mM) as an electron acceptor. To set up the experiments, cultures were grown to exponential phase aerobically.

Approximately ~105 cells were transferred into anaerobic media above and kept still during anaerobic incubation. The ferrozine assay was used to monitor Fe(III) reduction as previously described [24, 25]. Iron reduction rates were calculated by dividing the differences of Fe(II) concentrations by the differences of time intervals. Heme stain To detect the presence of c-type cytochromes, cells were grown anaerobically to the mid-log phase in LB medium supplemented with 50 mM sodium lactate, 20 mM fumarate and 10 mM ferric citrate and then centrifuged. The total cellular proteins were extracted from 0.2 ml cell culture using PeriPreps™ Periplasting kit (Epicentre, Madison, WI). The supernatant containing the cellular protein fraction was resuspended in SDS loading buffer and separated by SDS-PAGE using 12.5% polyacrylamide gels.