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Posttranslational Modification Influences the Effects of MgrA on norA Expression in Staphylococcus aureus

机译:翻译后修饰影响MgrA对金黄色葡萄球菌norA表达的影响。

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摘要

MgrA is a global regulator in Staphylococcus aureus. Differences in the effects of MgrA on norA expression have been reported for different strains, which varied in rsbU, a gene that affects the expression of sigB, which encodes an alternative σ factor involved in stress responses. We hypothesized that MgrA was modified by sigB-dependent factors that affected its ability to control the expression of the norA efflux pump. Heterologously expressed MgrA purified from Escherichia coli was incubated with crude extracts (CE) from strains RN6390 (rsbU) and SH1000 (rsbU+) and tested for binding to the norA promoter. Purified MgrA exhibited greater binding to norA promoter DNA after being incubated with SH1000 CE than MgrA incubated with the RN6390 CE. Phosphorylation of MgrA occurring in cell extracts caused it to lose the ability to bind norA promoter DNA. Overexpression of pknB, encoding a candidate serine/threonine kinase, produced increased phospho-MgrA and led to a fivefold increase in the transcript level of norA for both RN6390 and SH1000, as well as a fourfold increase in the MICs of norfloxacin and ciprofloxacin for these two strains. The levels of expression of pknB in RN6390 and SH1000, however, indicated that additional factors related to rsbU or sigB contribute to the differential regulatory effects of MgrA on norA expression.
机译:MgrA是金黄色葡萄球菌的全球调节剂。对于不同的菌株,已经报道了MgrA对norA表达的影响差异,该菌株在rsbU中发生变化,该基因影响sigB的表达,该基因编码参与应激反应的另一个σ因子。我们假设MgrA被sigB依赖性因子修饰,影响其控制norA外排泵表达的能力。从大肠杆菌中纯化的异源表达的MgrA与来自菌株RN6390(rsbU)和SH1000(rsbU + )的粗提物(CE)孵育,并测试其与norA启动子的结合。与SH1000 CE孵育后,纯化的MgrA与norA启动子DNA的结合要大于与RN6390 CE孵育的MgrA。细胞提取物中发生的MgrA磷酸化导致其失去结合norA启动子DNA的能力。编码候选丝氨酸/苏氨酸激酶的pknB的过表达产生增加的磷酸化MgrA,导致RN6390和SH1000的norA转录水平增加了五倍,而诺氟沙星和环丙沙星的MIC则增加了四倍。两个菌株。然而,RN6390和SH1000中pknB的表达水平表明,与rsbU或 sigB 相关的其他因素有助于MgrA对 norA 表达的差异调节作用。

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