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

被引:1386
作者
McClean, KH
Winson, MK
Fish, L
Taylor, A
Chhabra, SR
Camara, M
Daykin, M
Lamb, JH
Swift, S
Bycroft, BW
Stewart, GSAB
Williams, P
机构
[1] Univ Nottingham, Dept Pharmaceut Sci, Nottingham NG7 2RD, England
[2] Univ Nottingham, Dept Appl Biochem & Food Sci, Loughborough LE12 5RD, Leics, England
[3] Univ Leicester, MRC, Toxicol Unit, Leicester LE1 9HN, Leics, England
来源
MICROBIOLOGY-UK | 1997年 / 143卷
基金
英国惠康基金;
关键词
quorum sensing; N-acylhomoserine lactones; violacein; Chromobacterium violaceum; bioassay;
D O I
10.1099/00221287-143-12-3703
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 Cram-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 Cram-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. violaceun, 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 (ART) analogues. In CV026, violacein is inducible by all the AHL and AHT compounds evaluated with N-acyl side chains from C-4 to C-8 in length, with varying degrees of sensitivity. Although AHL compounds with N-acyl side chains from C-10 to C-14 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.
引用
收藏
页码:3703 / 3711
页数:9
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