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功能特征分析表明,结核分枝杆菌特异性蛋白激酶(Rv3080c)负责无毒性分枝杆菌的生长、吞噬和细胞内生存。

Functional characterization delineates that a Mycobacterium tuberculosis specific protein kinase (Rv3080c) is responsible for the growth, phagocytosis and intracellular survival of avirulent mycobacteria.

机构信息

Department of Microbiology, CSIR-Central Drug Research Institute, Lucknow, India.

出版信息

Mol Cell Biochem. 2012 Oct;369(1-2):67-74. doi: 10.1007/s11010-012-1369-9. Epub 2012 Jun 28.

Abstract

Serine/threonine protein kinases (STPKs) are predominantly involved in growth, development, division, differentiation, and in regulating immune responses in mycobacteria. A wide variety of functions of mycobacterial STPKs persuade mycobacterial growth and further its survival in the hosts. The polymorphic studies have shown that a full length gene of Rv3080c (pknK) is present in the slow growing mycobacteria. The wild type Mycobacterium smegmatis containing only vector (M. smegmatis) and M. smegmatis containing Rv3080c (pknK) cloned in pMV261 vector (M. smegmatis::K) were cultured in different growth media. The studies have shown that M. smegmatis did not differ in the growth and in survival while a substantial reduction in the growth (four-ten-folds) and a significant delay in the colony formation were observed in M. smegmatis::K. In order to look for the stage specific and modulated expression of PknK, the study was comprehended to quantitate pknK transcripts at different phases of cultures. The mycobacterium, containing high copy number of pknK specific RNA was unable to multiply. The study thus highlights that Rv3080c is largely accountable for changing the fate of avirulent mycobacteria and hence the protein can be utilized as an important molecule to target pathogenesis.

摘要

丝氨酸/苏氨酸蛋白激酶(STPKs)主要参与分枝杆菌的生长、发育、分裂、分化以及免疫反应的调节。分枝杆菌 STPK 的多种功能促使分枝杆菌生长并使其在宿主中存活。多态性研究表明,生长缓慢的分枝杆菌中存在全长基因 Rv3080c(pknK)。含有载体的野生型耻垢分枝杆菌(M. smegmatis)(M. smegmatis)和含有克隆在 pMV261 载体中的 Rv3080c(pknK)的耻垢分枝杆菌(M. smegmatis::K)在不同的生长培养基中培养。研究表明,M. smegmatis 在生长和存活方面没有差异,而 M. smegmatis::K 的生长(四到十倍)显著减少,菌落形成明显延迟。为了寻找 PknK 的特定阶段和调节表达,研究旨在定量检测培养不同阶段的 pknK 转录本。含有高拷贝数 pknK 特异性 RNA 的分枝杆菌无法繁殖。因此,该研究强调 Rv3080c 在很大程度上决定了无毒分枝杆菌的命运,因此该蛋白可作为靶向发病机制的重要分子。

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