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结核分枝杆菌毒素 Rv2872 是一种 RNase,参与万古霉素应激反应和生物膜形成。

Mycobacterium tuberculosis toxin Rv2872 is an RNase involved in vancomycin stress response and biofilm development.

机构信息

Institute of Modern Biopharmaceuticals, State Key Laboratory Breeding Base of Eco-Environment and Bio-Resource of the Three Gorges Area, Key Laboratory of Eco-environments in Three Gorges Reservoir Region, Ministry of Education, School of Life Sciences, Southwest University, Beibei, Chongqing, 400715, China.

出版信息

Appl Microbiol Biotechnol. 2018 Aug;102(16):7123-7133. doi: 10.1007/s00253-018-9132-0. Epub 2018 Jun 11.

Abstract

Bacterial toxin-antitoxin (TA) systems are emerging important regulators of multiple cellular physiological events and candidates for novel antibiotic targets. To explore the role of Mycobacterium tuberculosis function, unknown toxin gene Rv2872 was heterologously expressed in Mycobacterium smegmatis (MS_Rv2872). Upon induction, MS_Rv2872 phenotype differed significantly from the control, such as increased vancomycin resistance, retarded growth, cell wall, and biofilm structure. This phenotype change might result from the RNase activity of Rv2872 as purified Rv2872 toxin protein can cleave the products of several key genes involved in abovementioned phenotypes. In summary, toxin Rv2872 was firstly reported to be a endonuclease involved in antibiotic stress responses, cell wall structure, and biofilm development.

摘要

细菌毒素-抗毒素 (TA) 系统是新兴的重要细胞生理事件调节剂,也是新型抗生素靶标的候选者。为了探索分枝杆菌功能,我们在耻垢分枝杆菌中异源表达了结核分枝杆菌未知毒素基因 Rv2872(MS_Rv2872)。诱导后,MS_Rv2872 的表型与对照相比有明显差异,如万古霉素耐药性增加、生长缓慢、细胞壁和生物膜结构改变。这种表型变化可能是由于 Rv2872 的 RNase 活性所致,因为纯化的 Rv2872 毒素蛋白可以切割涉及上述表型的几个关键基因的产物。总之,我们首次报道毒素 Rv2872 是一种参与抗生素应激反应、细胞壁结构和生物膜形成的内切核酸酶。

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