, 2010). As almost all halophilic microorganisms have potential Na+ ion transport mechanisms

to expel Na+ ions from the interior of the cells depending on Na+/H+ antiporters (Oren, 1999), it is very likely that some important (even ERK inhibitor libraries novel) Na+/H+ antiporter genes exist in the above area containing such many potential novel species. To obtain as many (especially novel) Na+/H+ antiporter genes as possible, metagenomic DNA was screened from the culturable halophilic bacteria in the above area and several genes with Na+/H+ antiport activity were finally cloned. Of these, psmrAB were found to encode a pair of putative PSMR family proteins, the homolog of YvdSR in B. subtilis. In this

study, we reported the cloning and characterization of psmrAB and finally proposed that PsmrAB should function mainly as a novel two-component Na+/H+ antiporter. Halophilic bacteria were enriched in the Sehgal–Gibbons medium containing 0.5% casein, 1% yeast extract, 0.5% tryptone, 0.2% KCl, 0.3% trisodium citrate, 2% MgSO4. 7H2O plus 7.5% NaCl at pH 7.5. Escherichia coli strain KNabc, lacking three major Na+/H+ antiporters (NhaA, NhaB and ChaA) and its transformant cells were grown in the LBK medium consisting of 1.0% tryptone, 0.5% yeast extract and 87 mM KCl, to which NaCl or LiCl was added at indicated concentrations when necessary. Ampicillin was added to a final concentration of 50 μg mL−1 for O-methylated flavonoid the selection selleck products of transformant cells. To test the resistance of PsmrAB to the antimicrobial drugs, E. coli DH5α/pEASY T3-psmrAB and DH5α/pEASY T3 (as a negative control) were grown overnight on the LB medium plates and then continued to be grown on the fresh LB medium plates containing the different concentrations of drugs for 48 h. Cell growth was monitored turbidimetrically

at 600 nm. A 5-mL overnight culture of E. coli KNabc or DH5α cells was inoculated into 100 mL of LBK or LB medium and grown to an optimal density of 0.4 at 600 nm. Cells were harvested by centrifugation at 4000 g for 10 min at 4 °C and washed for three times in 10 mL of ice-cold sterile 10% glycerol solution before electro-competent preparation. Recombinant plasmids (20–200 ng) were added to 50–200 μL of cell suspension and mixed thoroughly. Electroporation was carried out at a field strength of 16 kV cm−1 in combination with an electric resistance of 300 Ω at 25 mF in a 0.1-cm electroporation cuvette. Soil samples (20-cm deep) were widely collected around Daban Salt Lake in Xinjiang Province, P.R. China, and then the culturable halophilic bacteria were enriched in the Sehgal–Gibbons medium containing 7.5% NaCl. The metagenomic DNA was extracted from the enriched cultures and partially digested with Sau3AI.