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群体感应与紫色色杆菌:利用紫色菌素的产生与抑制来检测N-酰基高丝氨酸内酯

Quorum sensing and Chromobacterium violaceum: exploitation of violacein production and inhibition for the detection of N-acylhomoserine lactones.

作者信息

McClean Kay H, Winson Michael K, Fish Leigh, Taylor Adrian, Chhabra Siri Ram, Camara Miguel, Daykin Mavis, Lamb John H, Swift Simon, Bycroft Barrie W, Stewart Gordon S A B, Williams Paul

机构信息

Department of Pharmaceutical Sciences, University of Nottingham, University Park, Nottingham NG7 2RD, UK.

Department of Applied Biochemistry and Food Science, University of Nottingham, Sutton Bonington Campus, Loughborough LE12 5RD, UK.

出版信息

Microbiology (Reading). 1997 Dec;143 ( Pt 12):3703-3711. doi: 10.1099/00221287-143-12-3703.

Abstract

Quorum sensing relies upon the interaction of a diffusible signal molecule with a transcriptional activator protein to couple gene expression with cell population density. In Gram-negative bacteria, such signal molecules are usually N-acylhomoserine lactones (AHLs) which differ in the structure of their N-acyl side chains. Chromobacterium violaceum, a Gram-negative bacterium commonly found in soil and water, produces the characteristic purple pigment violacein. Previously the authors described a violacein-negative, mini-Tn5 mutant of C. violaceum (CV026) in which pigment production can be restored by incubation with supernatants from the wild-type strain. To develop this mutant as a general biosensor for AHLs, the natural C. violaceum AHL molecule was first chemically characterized. By using solvent extraction, HPLC and mass spectrometry, a single AHL, N-hexanoyl-L-homoserine lactone (HHL), was identified in wild-type C. violaceum culture supernatants which was absent from CV026. Since the production of violacein constitutes a simple assay for the detection of AHLs, we explored the ability of CV026 to respond to a series of synthetic AHL and N-acylhomocysteine thiolactone (AHT) analogues. In CV026, violacein is inducible by all the AHL and AHT compounds evaluated with N-acyl side chains from C4 to C8 in length, with varying degrees of sensitivity. Although AHL compounds with N-acyl side chains from C10 to C14 are unable to induce violacein production, if an activating AHL (e.g. HHL) is incorporated into the agar, these long-chain AHLs can be detected by their ability to inhibit violacein production. The versatility of CV026 in facilitating detection of AHL mixtures extracted from culture supernatants and separated by thin-layer chromatography is also demonstrated. These simple bioassays employing CV026 thus greatly extend the ability to detect a wide spectrum of AHL signal molecules.

摘要

群体感应依赖于一种可扩散信号分子与转录激活蛋白的相互作用,从而将基因表达与细胞群体密度联系起来。在革兰氏阴性细菌中,这类信号分子通常是N-酰基高丝氨酸内酯(AHLs),其N-酰基侧链结构有所不同。紫色杆菌是一种常见于土壤和水中的革兰氏阴性细菌,可产生特征性紫色色素紫菌素。此前,作者描述了一种紫色杆菌(CV026)的紫菌素阴性mini-Tn5突变体,将其与野生型菌株的上清液一起孵育可恢复色素生成。为了将该突变体开发成一种通用的AHL生物传感器,首先对天然紫色杆菌AHL分子进行了化学表征。通过溶剂萃取、高效液相色谱和质谱分析,在野生型紫色杆菌培养上清液中鉴定出一种单一AHL,即N-己酰基-L-高丝氨酸内酯(HHL),而CV026中不存在该物质。由于紫菌素的产生构成了一种检测AHLs的简单测定方法,我们探究了CV026对一系列合成AHL和N-酰基高半胱氨酸硫内酯(AHT)类似物的响应能力。在CV026中,所有评估的AHL和AHT化合物(N-酰基侧链长度从C4到C8)都能诱导紫菌素生成,只是敏感度不同。虽然N-酰基侧链长度从C10到C14的AHL化合物无法诱导紫菌素生成,但如果将一种激活型AHL(如HHL)加入琼脂中,这些长链AHLs可通过抑制紫菌素生成的能力被检测到。还证明了CV026在促进检测从培养上清液中提取并通过薄层色谱分离的AHL混合物方面的通用性。因此,这些采用CV026的简单生物测定法极大地扩展了检测多种AHL信号分子的能力。

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