首页> 美国卫生研究院文献>Journal of Bacteriology >Contribution of the PhoP-PhoQ and PmrA-PmrB Two-Component Regulatory Systems to Mg2+-Induced Gene Regulation in Pseudomonas aeruginosa
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Contribution of the PhoP-PhoQ and PmrA-PmrB Two-Component Regulatory Systems to Mg2+-Induced Gene Regulation in Pseudomonas aeruginosa

机译:PhoP-PhoQ和PmrA-PmrB两组分调节系统对铜绿假单胞菌中Mg2 +诱导的基因调节的贡献。

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摘要

When grown in divalent cation-limited medium, Pseudomonas aeruginosa becomes resistant to cationic antimicrobial peptides and polymyxin B. This resistance is regulated by the PhoP-PhoQ and PmrA-PmrB two-component regulatory systems. To further characterize Mg2+ regulation in P. aeruginosa, microarray transcriptional profiling was conducted to compare wild-type P. aeruginosa grown under Mg2+-limited and Mg2+-replete conditions to isogenic phoP and pmrA mutants grown under Mg2+-limited conditions. Under Mg2+-limited conditions (0.02 mM Mg2+), approximately 3% of the P. aeruginosa genes were differentially expressed compared to the expression in bacteria grown under Mg2+-replete conditions (2 mM Mg2+). Only a modest subset of the Mg2+-regulated genes were regulated through either PhoP or PmrA. To determine which genes were directly regulated, a bioinformatic search for conserved binding motifs was combined with confirmatory reverse transcriptase PCR and gel shift promoter binding assays, and the results indicated that very few genes were directly regulated by these response regulators. It was found that in addition to the previously known oprH-phoP-phoQ operon and the pmrHFIJKLM-ugd operon, the PA0921 and PA1343 genes, encoding small basic proteins, were regulated by Mg2+ in a PhoP-dependent manner. The number of known PmrA-regulated genes was expanded to include the PA1559-PA1560, PA4782-PA4781, and feoAB operons, in addition to the previously known PA4773-PA4775-pmrAB and pmrHFIJKLM-ugd operons.
机译:在二价阳离子受限培养基中生长时,铜绿假单胞菌对阳离子抗菌肽和多粘菌素B产生抗药性。该抗药性由PhoP-PhoQ和PmrA-PmrB两组分调节系统调节。为了进一步表征铜绿假单胞菌中Mg 2 + 的调控,进行了微阵列转录谱分析,比较了在Mg 2 + 限制和Mg 2 + 限制条件下生长的等基因phoP和pmrA突变体的> 2 + 充分条件。在Mg 2 + 限制条件下(0.02 mM Mg 2 + ),与在Mg下生长的细菌中的表达相比,大约有3%的铜绿假单胞菌基因差异表达。 2 + -完全条件(2 mM Mg 2 + )。 Mg 2 + 调控基因中只有一小部分是通过PhoP或PmrA调控的。为了确定哪些基因被直接调控,将生物信息学搜索保守的结合基序与证实性逆转录酶PCR和凝胶移位启动子结合测定相结合,结果表明很少有基因被这些反应调控因子直接调控。发现除了先前已知的oprH-phoP-phoQ操纵子和pmrHFIJKLM-ugd操纵子外,编码小碱性蛋白的PA0921和PA1343基因在PhoP中还受Mg 2 + 的调控。依赖的方式。除了先前已知的PA4773-PA4775-pmrAB和pmrHFIJKLM-ugd操纵子之外,已知的PmrA调控基因的数量已扩展到包括PA1559-PA1560,PA4782-PA4781和feoAB操纵子。

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