受 MtrAB 和 MprAB 调控的粘蛋白内肽酶 MepA 参与细胞壁的平衡。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-07-01 DOI:10.1016/j.resmic.2024.104188
Feng Peng , Yu Zou , Xiuxia Liu , Yankun Yang , Jing Chen , Jianqi Nie , Danni Huang , Zhonghu Bai
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引用次数: 0

摘要

谷氨酸棒状杆菌的完整基因组中含有一个编码金黄色葡萄蛋白内肽酶 MepA 的基因,该基因通过调节肽聚糖的生物合成来维持细胞壁的平衡。本研究对 MepA 的生理功能、定位和调节因子进行了研究。结果表明,过表达 MepA 会导致肽聚糖降解和细胞分裂缺陷。结果表明,MepA-mCherry只定位在细胞隔。此外,mepA 的过表达增加了细胞的通透性,降低了细胞对异烟肼(一种用于治疗结核分枝杆菌感染的抗生素)的抗性。此外,转录分析表明,mepA影响细胞分裂和膜运输途径,并受双组分系统MtrAB和MprAB(CgtS/R2)的协调调控。
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The murein endopeptidase MepA regulated by MtrAB and MprAB participate in cell wall homeostasis

The complete genome of Corynebacterium glutamicum contain a gene encoding murein endopeptidase MepA which maintain cell wall homeostasis by regulating peptidoglycan biosynthesis. In this study, we investigate the physiological function, localization and regulator of MepA. The result shows that mepA overexpression lead to peptidoglycan degradation and the defects in cell division. MepA-EGFP was shown to localizes exclusively at the cell cell septum. In addition, mepA overexpression increased cell permeability and reduced the resistance of cells to isoniazid, an antibiotic used to treat Mycobacterium tuberculosis infection. Furthermore, transcription analysis showed that mepA affected cell division and membrane transport pathways, and was coordinately regulated by the two-component systems MtrAB and MprAB(CgtS/R2).

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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