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

机译:法定传感和富集型紫杉杆菌:利用紫杉蛋白的生产和抑制对N-酰基骨晶内酯的抑制作用

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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 pigmen 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 ail 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 signa molecules.
机译:致法感测量依赖于扩散信号分子与转录活化剂蛋白的相互作用,以耦合具有细胞群密度的基因表达。在革兰氏阴性细菌中,这种信号分子通常是N-酰基胚层内酯(AHL),其在其N-酰基侧链的结构中不同。紫杉杆菌,常见于土壤和水中常见的革兰氏阴性细菌,产生特色紫色猪紫薇。此前,作者描述了C. violateum(CV026)的violapein-阴性Mini-TN5突变体,其中可以通过与野生型菌株的上清液孵育来恢复颜料产生。为了将该突变体作为AHLS的一般生物传感器,首先是化学表征的天然C.Fortaceum AHL分子。通过使用溶剂萃取,HPLC和质谱法,在野生型C.紫外线培养上清液中鉴定单个AHL,N-己酰基-L-HOMOSERINE内酯内酯内酯(HHL),其不存在CV026。由于紫杉蛋白的生产构成了用于检测AHL的简单测定,因此我们探讨了CV026响应了一系列合成AHL和N-酰基核细胞硫内酯(AHT)类似物的能力。在CV026中,Violapein通过与N-酰基侧链的AHL和AHT化合物从C4至C8的长度评价的AIL和AHT化合物诱导,具有不同程度的敏感性。尽管来自C10至C14的N-酰基侧链的AHL化合物不能诱导紫杉蛋白产生,但是,如果将活化的AHL(例如HHL)掺入琼脂中,则可以通过其抑制紫杉蛋白产生的能力来检测这些长链AHL。还证明了CV026在促进从培养上清液中提取的AHL混合物进行检测并通过薄层色谱分离的多功能性。因此,使用CV026的简单生物大大延长了检测宽光谱的AHL Signa分子的能力。

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