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万古霉素不影响纯化的 VanSA 的酶活性。

Vancomycin does not affect the enzymatic activities of purified VanSA.

机构信息

Department of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, Pennsylvania, United States of America.

出版信息

PLoS One. 2019 Jan 24;14(1):e0210627. doi: 10.1371/journal.pone.0210627. eCollection 2019.

Abstract

VanS is a membrane-bound sensor histidine kinase responsible for sensing vancomycin and activating transcription of vancomycin-resistance genes. In the presence of vancomycin, VanS phosphorylates the transcription factor VanR, converting it to its transcriptionally active form. In the absence of vancomycin, VanS dephosphorylates VanR, thereby maintaining it in a transcriptionally inactive state. To date, the mechanistic details of how vancomycin modulates VanS activity have remained elusive. We have therefore studied these details in an in vitro system, using the full-length VanS and VanR proteins responsible for type-A vancomycin resistance in enterococci. Both detergent- and amphipol-solubilized VanSA display all the enzymatic activities expected for a sensor histidine kinase, with amphipol reconstitution providing a marked boost in overall activity relative to detergent solubilization. A putative constitutively activated VanSA mutant (T168K) was constructed and purified, and was found to exhibit the expected reduction in phosphatase activity, providing confidence that detergent-solubilized VanSA behaves in a physiologically relevant manner. In both detergent and amphipol solutions, VanSA's enzymatic activities were found to be insensitive to vancomycin, even at levels many times higher than the antibiotic's minimum inhibitory concentration. This result argues against direct activation of VanSA via formation of a binary antibiotic-kinase complex, suggesting instead that either additional factors are required to form a functional signaling complex, or that activation does not require direct interaction with the antibiotic.

摘要

VanS 是一种膜结合的传感器组氨酸激酶,负责感应万古霉素并激活万古霉素耐药基因的转录。在万古霉素存在的情况下,VanS 使转录因子 VanR 磷酸化,将其转化为转录活性形式。在没有万古霉素的情况下,VanS 去磷酸化 VanR,从而使其保持在转录非活性状态。迄今为止,万古霉素如何调节 VanS 活性的机制细节仍然难以捉摸。因此,我们使用负责肠球菌 A 型万古霉素耐药的全长 VanS 和 VanR 蛋白在体外系统中研究了这些细节。去污剂和两亲聚合物溶解的 VanSA 均显示出传感器组氨酸激酶所期望的所有酶活性,与去污剂溶解相比,两亲聚合物的重建提供了整体活性的显著提高。构建并纯化了一种假定的组成型激活的 VanSA 突变体(T168K),并发现其磷酸酶活性预期降低,这表明去污剂溶解的 VanSA 以生理相关的方式发挥作用。在去污剂和两亲聚合物溶液中,VanSA 的酶活性对万古霉素不敏感,即使在远高于抗生素最低抑菌浓度的水平下也是如此。这一结果表明,VanSA 不是通过形成二元抗生素-激酶复合物直接激活,这表明形成功能性信号复合物需要其他因素,或者激活不需要与抗生素直接相互作用。

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