Suppr超能文献

谷氨酸棒杆菌中全局调控因子SugR对磷酸烯醇丙酮酸:糖磷酸转移酶系统(PTS)一般组分表达的调控

Regulation of expression of general components of the phosphoenolpyruvate: carbohydrate phosphotransferase system (PTS) by the global regulator SugR in Corynebacterium glutamicum.

作者信息

Tanaka Yuya, Teramoto Haruhiko, Inui Masayuki, Yukawa Hideaki

机构信息

Research Institute of Innovative Technology for the Earth, 9-2, Kizugawadai, Kizugawa, Kyoto, 619-0292, Japan.

出版信息

Appl Microbiol Biotechnol. 2008 Feb;78(2):309-18. doi: 10.1007/s00253-007-1313-1. Epub 2008 Jan 9.

Abstract

The phosphoenolpyruvate: carbohydrate phosphotransferase system (PTS) catalyzes transport of carbohydrates by coupling carbohydrate translocation and phosphorylation. Enzyme I and HPr, encoded in ptsI and ptsH, respectively, are cytoplasmic proteins commonly used for transport of variety of PTS sugars. In this study, we investigated the role of SugR on the expression of the ptsI and ptsH which increases in the presence of PTS sugars in Corynebacterium glutamicum. Disruption of sugR resulted in the increased expression of ptsI and ptsH in the absence of PTS sugar. Introduction of a plasmid containing sugR gene complemented the effect of sugR disruption. SugR was purified and binding to the promoter regions of ptsI and ptsH was indicated by EMSA. DNase I footprinting analysis indicated the binding sites of SugR on the promoter region of divergently transcribed ptsI gene and fructose-pts operon. The binding sites contain a possible SugR binding motif which is conserved in the promoter regions of general and sugar-specific pts genes. Mutations in this motif resulted in the decrease of SugR binding to the ptsI promoter. These results suggest that SugR represses ptsI and ptsH in the absence of PTS sugar and derepression is the mechanism for the induction of the general components of PTS.

摘要

磷酸烯醇丙酮酸

碳水化合物磷酸转移酶系统(PTS)通过耦合碳水化合物转运和磷酸化来催化碳水化合物的运输。分别由ptsI和ptsH编码的酶I和HPr是细胞质蛋白,常用于多种PTS糖类的运输。在本研究中,我们调查了SugR在谷氨酸棒杆菌中对ptsI和ptsH表达的作用,这两个基因在PTS糖类存在时表达增加。sugR的缺失导致在没有PTS糖类的情况下ptsI和ptsH的表达增加。引入含有sugR基因的质粒可弥补sugR缺失的影响。SugR被纯化,电泳迁移率变动分析(EMSA)表明其与ptsI和ptsH的启动子区域结合。DNase I足迹分析表明SugR在反向转录的ptsI基因和果糖-pts操纵子启动子区域的结合位点。这些结合位点包含一个可能的SugR结合基序,该基序在一般和糖特异性pts基因的启动子区域中保守。该基序中的突变导致SugR与ptsI启动子的结合减少。这些结果表明,在没有PTS糖类的情况下,SugR抑制ptsI和ptsH,去阻遏是PTS一般组分诱导的机制。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验