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首页> 外文期刊>BMC Microbiology >LuxS-independent formation of AI-2 from ribulose-5-phosphate
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LuxS-independent formation of AI-2 from ribulose-5-phosphate

机译:不依赖LuxS的核糖5磷酸形成AI-2

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In many bacteria, the signal molecule AI-2 is generated from its precursor S-ribosyl-L-homocysteine in a reaction catalysed by the enzyme LuxS. However, generation of AI-2-like activity has also been reported for organisms lacking the luxS gene and the existence of alternative pathways for AI-2 formation in Escherichia coli has recently been predicted by stochastic modelling. Here, we investigate the possibility that spontaneous conversion of ribulose-5-phosphate could be responsible for AI-2 generation in the absence of luxS. Buffered solutions of ribulose-5-phosphate, but not ribose-5-phosphate, were found to contain high levels of AI-2 activity following incubation at concentrations similar to those reported in vivo. To test whether this process contributes to AI-2 formation by bacterial cells in vivo, an improved Vibrio harveyi bioassay was used. In agreement with previous studies, culture supernatants of E. coli and Staphylococcus aureus luxS mutants were found not to contain detectable levels of AI-2 activity. However, low activities were detected in an E. coli pgi-eda-edd-luxS mutant, a strain which degrades glucose entirely via the oxidative pentose phosphate pathway, with ribulose-5-phosphate as an obligatory intermediate. Our results suggest that LuxS-independent formation of AI-2, via spontaneous conversion of ribulose-5-phosphate, may indeed occur in vivo. It does not contribute to AI-2 formation in wildtype E. coli and S. aureus under the conditions tested, but may be responsible for the AI-2-like activities reported for other organisms lacking the luxS gene.
机译:在许多细菌中,信号分子AI-2由其前体S-核糖基-L-高半胱氨酸在酶LuxS催化的反应中产生。然而,也已经报道了缺少luxS基因的生物体会产生类似AI-2的活性,最近通过随机建模预测了在大肠杆菌中AI-2形成的替代途径的存在。在这里,我们调查在没有luxS的情况下,核糖5磷酸的自发转化可能是AI-2产生的原因。孵育后发现核糖5磷酸而不是5核糖5的缓冲溶液含有高水平的AI-2活性,其浓度与体内报道的浓度相似。为了测试此过程是否有助于体内细菌细胞形成AI-2,使用了改良的哈维弧菌生物测定法。与先前的研究一致,发现大肠杆菌和金黄色葡萄球菌luxS突变体的培养上清液不包含可检测水平的AI-2活性。然而,在大肠杆菌pgi-eda-edd-luxS突变体中检测到低活性,该菌株完全通过氧化戊糖磷酸途径降解葡萄糖,而核糖-5-磷酸是必需中间体。我们的结果表明,可能会在体内发生不依赖LuxS的AI-2的形成,即通过5磷酸核糖的自发转化。在所测试的条件下,它不会促进野生型大肠杆菌和金黄色葡萄球菌中AI-2的形成,但可能与报道的其他缺少luxS基因的生物的AI-2类活性有关。

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