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基于无细胞大肠杆菌的系统,用于筛选与天蓝色链霉菌群体感应受体蛋白相互作用的群体感应分子。

Cell-free Escherichia coli-based system to screen for quorum-sensing molecules interacting with quorum receptor proteins of Streptomyces coelicolor.

作者信息

Yang Yung-Hun, Kim Tae-Wan, Park Sung-Hee, Lee Kwangwon, Park Hyung-Yeon, Song Eunjung, Joo Hwang-Soo, Kim Yun-Gon, Hahn Ji-Sook, Kim Byung-Gee

机构信息

School of Chemical and Biological Engineering, Seoul National University, Seoul, Republic of Korea.

出版信息

Appl Environ Microbiol. 2009 Oct;75(19):6367-72. doi: 10.1128/AEM.00019-09. Epub 2009 Aug 14.

Abstract

Quorum sensing (QS) is mediated by small molecules and involved in diverse cellular functions, such as virulence, biofilm formation, secondary metabolism, and cell differentiation. In this study, we developed a rapid and effective screening tool based on a cell-free Escherichia coli-based expression system to identify QS molecules of Streptomyces. The binding of QS molecules to gamma-butyrolactone receptor ScbR was monitored by changes in the expression levels of the green fluorescent protein reporter in E. coli cell extract. Using this assay system, we could successfully confirm SCB1, a gamma-butyrolactone molecule in Streptomyces coelicolor, binding to its known receptor, ScbR. In addition, we have shown that N-hexanoyl-DL-homoserine lactone, one of the QS molecules in many gram-negative bacteria, can regulate ScbR and trigger precocious antibiotic production in S. coelicolor. Our new method can be applied to other strains for which a screening tool for QS molecules has not yet been developed.

摘要

群体感应(QS)由小分子介导,并参与多种细胞功能,如毒力、生物膜形成、次级代谢和细胞分化。在本研究中,我们基于无细胞的大肠杆菌表达系统开发了一种快速有效的筛选工具,以鉴定链霉菌的QS分子。通过大肠杆菌细胞提取物中绿色荧光蛋白报告基因表达水平的变化来监测QS分子与γ-丁内酯受体ScbR的结合。使用该检测系统,我们成功证实了天蓝色链霉菌中的γ-丁内酯分子SCB1与其已知受体ScbR的结合。此外,我们还表明,许多革兰氏阴性细菌中的QS分子之一N-己酰-DL-高丝氨酸内酯可以调节ScbR并触发天蓝色链霉菌中早熟抗生素的产生。我们的新方法可应用于尚未开发QS分子筛选工具的其他菌株。

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