Table S1 Bacterial strains and plasmids used in this study Tabl

Table S1. Bacterial strains and plasmids used in this study. Table S2. PCR primers used in this study. Table S3. Sensitivity of S. sahachiroi ATCC 33158 to antibiotics. Table S4. Effect of culture temperature on protoplast formation and regeneration. Table S5. Effect of regeneration media on protoplast regeneration. “
“Two independent cervimycin C (CmC)-resistant clones of Bacillus subtilis were identified, each carrying two mutations in the intergenic region preceding the ABC transporter gene bmrA. In the double mutant, real-time PCR revealed an increased amount of bmrA mRNA with increased stability. Accordingly, isolation of

membrane proteins yielded a strong band at 64 kDa corresponding to BmrA. Analyses showed that one mutation Erastin nmr optimized the −35 box sequence conferring resistance to 3 μM CmC, while the +6 mutation alone had no effect, but increased the potential of the strain harboring the −35 mutation to grow at 5 μM CmC. Transcriptional fusions revealed an elevated bmrA promoter activity for the double mutant. Electrophoretic mobility shift assays (EMSAs) confirmed a 30-fold higher binding affinity of RNA polymerase for this mutant compared with the wild type, and the effect was due to the −35 box alteration of the bmrA promoter. In vitro transcription

experiments substantiated the results of the EMSA. EMSAs in the presence of heparin indicated that the mutations did not influence the formation and/or the stability of open complexes. Half-life measurements demonstrated Ion Channel Ligand Library that the +6 mutation stabilized bmrA mRNA ≈2-fold. Overall, we found that an ABC transporter confers antibiotic resistance by the cumulative effects of two mutations in the promoter region. Cervimycin C (CmC) belongs to a complex of compounds produced by Streptomyces tendae and consists of a tetracyclic polyketide

decorated with Histone demethylase trideoxysugar chains, solely active against Gram-positive bacteria (Herold et al., 2005). Generally, microorganisms are able to adapt to antibiotic stress by a variety of specific and unspecific mechanisms (Wright, 2000). A more general mechanism affecting hydrophobic drugs is exerted by exporters lowering intracellular drug concentrations either acting as antiporters or by ATP hydrolysis-driven export (Kerr et al., 2005). Ohki & Tateno (2004) described the increased stability of the multidrug efflux transporter bmr3 mRNA resulting in a multidrug-resistant phenotype in Bacillus subtilis. Bacillus subtilis possesses a number of genes belonging to the ABC exporters. One of these is BmrA, which was shown in vitro to export ethidium bromide and doxorubicin (Steinfels et al., 2004). However, despite a detailed description of structural and functional features, so far, no biologically relevant substrate or function of BmrA has been identified (Chami et al., 2002; Orelle et al., 2003; Steinfels et al., 2004; Ravaud et al., 2006; Orelle et al., 2008). For analysis of the genetic changes, whole-genome sequencing can be applied.

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