Zhu J, Beaber J W, Moré M I, Fuqua C, Eberhard A, Winans S C
Section of Microbiology, Cornell University, Ithaca, New York 14853, USA.
J Bacteriol. 1998 Oct;180(20):5398-405. doi: 10.1128/JB.180.20.5398-5405.1998.
The TraR and TraI proteins of Agrobacterium tumefaciens mediate cell-density-dependent expression of the Ti plasmid tra regulon. TraI synthesizes the autoinducer pheromone N-(3-oxooctanoyl)-L-homoserine lactone (3-oxo-C8-HSL), while TraR is an 3-oxo-C8-HSL-responsive transcriptional activator. We have compared the abilities of 3-oxo-C8-HSL and 32 related compounds to activate expression of a TraR-regulated promoter. In a strain that expresses wild-type levels of TraR, only 3-oxo-C8-HSL was strongly stimulatory, four compounds were detectably active only at high concentrations, and the remaining 28 compounds were inactive. Furthermore, many of these compounds were potent antagonists. In contrast, almost all of these compounds were stimulatory in a congenic strain that overexpresses TraR and no compound was a potent antagonist. We propose a model in which autoinducers enhance the affinity of TraR either for other TraR monomers or for DNA binding sites and that overexpression of TraR potentiates this interaction by mass action. Wild-type A. tumefaciens released a rather broad spectrum of autoinducers, including several that antagonize induction of a wild-type strain. However, under all conditions tested, 3-oxo-C8-HSL was more abundant than any other analog, indicating that other released autoinducers do not interfere with tra gene induction. We conclude that (i) in wild-type strains, only 3-oxo-C8-HSL significantly stimulates tra gene expression, while many autoinducer analogs are potent antagonists; (ii) TraR overexpression increases agonistic activity of autoinducer analogs, allowing sensitive biodetection of many autoinducers; and (iii) autoinducer stimulatory activity is potentiated by TraR overproduction, suggesting that autoinducers may shift an equilibrium between TraR monomers and dimers or oligomers. When autoinducer specificities of other quorum-sensing proteins are tested, care should be taken not to overexpress those proteins.
根癌土壤杆菌的TraR和TraI蛋白介导Ti质粒tra操纵子的细胞密度依赖性表达。TraI合成自诱导信号分子N-(3-氧代辛酰基)-L-高丝氨酸内酯(3-氧代-C8-HSL),而TraR是一种对3-氧代-C8-HSL有反应的转录激活因子。我们比较了3-氧代-C8-HSL和32种相关化合物激活TraR调控启动子表达的能力。在表达野生型水平TraR的菌株中,只有3-氧代-C8-HSL具有强烈的刺激作用,4种化合物仅在高浓度时才有可检测到的活性,其余28种化合物无活性。此外,这些化合物中有许多是强效拮抗剂。相比之下,在一个过表达TraR的同基因菌株中,几乎所有这些化合物都具有刺激作用,且没有化合物是强效拮抗剂。我们提出了一个模型,其中自诱导信号分子增强了TraR对其他TraR单体或DNA结合位点的亲和力,并且TraR的过表达通过质量作用增强了这种相互作用。野生型根癌土壤杆菌释放出相当广泛的自诱导信号分子,包括几种对野生型菌株诱导有拮抗作用的分子。然而,在所有测试条件下,3-氧代-C8-HSL比任何其他类似物都更丰富,这表明其他释放的自诱导信号分子不会干扰tra基因的诱导。我们得出以下结论:(i)在野生型菌株中,只有3-氧代-C8-HSL能显著刺激tra基因表达,而许多自诱导信号分子类似物是强效拮抗剂;(ii)TraR的过表达增加了自诱导信号分子类似物的激动活性,从而能够灵敏地生物检测许多自诱导信号分子;(iii)TraR的过量产生增强了自诱导信号分子的刺激活性,这表明自诱导信号分子可能会改变TraR单体与二聚体或寡聚体之间的平衡。在测试其他群体感应蛋白的自诱导信号分子特异性时,应注意不要过度表达这些蛋白。