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Cell-Free Escherichia coli-Based System To Screen for Quorum-Sensing Molecules Interacting with Quorum Receptor Proteins of Streptomyces coelicolor

机译:基于无细胞大肠埃希氏菌的系统,用于筛选与天蓝色链霉菌的群体受体蛋白相互作用的群体传感分子

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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 γ-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 γ-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.
机译:群体感应(QS)由小分子介导,并参与多种细胞功能,例如毒力,生物膜形成,次级代谢和细胞分化。在这项研究中,我们开发了一种基于无细胞大肠杆菌表达系统的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,监测QS分子与γ-丁内酯受体ScbR的结合。使用该测定系统,我们可以成功地确认天蓝色链霉菌中的γ-丁内酯分子SCB1与其已知受体ScbR结合。另外,我们已经表明,N-己酰基-dl-高丝氨酸内酯(许多革兰氏阴性细菌中的QS分子之一)可以调节ScbR并触发腔肠链球菌的早熟抗生素生产。我们的新方法可以应用于尚未开发QS分子筛选工具的其他菌株。

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