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磷酸烯醇丙酮酸:果糖磷酸转移酶系统对流感嗜血杆菌Rd感受态发育和糖利用的调控

Regulation of competence development and sugar utilization in Haemophilus influenzae Rd by a phosphoenolpyruvate:fructose phosphotransferase system.

作者信息

Macfadyen L P, Dorocicz I R, Reizer J, Saier M H, Redfield R J

机构信息

Department of Zoology, University of British Columbia, Vancouver, Canada.

出版信息

Mol Microbiol. 1996 Sep;21(5):941-52. doi: 10.1046/j.1365-2958.1996.441420.x.

Abstract

Changes in intracellular cAMP concentration play important roles in Haemophilus influenzae, regulating both sugar utilization and competence for natural transformation. In enteric bacteria, cAMP levels are controlled by the phosphoenolpyruvate:glycose phosphotransferase system (PTS) in response to changes in availability of the preferred sugars it transports. We have demonstrated the existence of a simple PTS in H. influenzae by several methods. We have cloned the H. influenzae ptsI gene, encoding PTS Enzyme I; genome analysis locates it in a pts operon structurally homologous to those of enteric bacteria. In vitro phosphorylation assays confirmed the presence of functional PTS components. A ptsI null mutation reduced fructose uptake to 1% of the wild-type rate, and abolished fructose fermentation even when exogenous cAMP was provided. The ptsI mutation also prevented fermentation of ribose and galactose, but utilization of these cAMP-dependent sugars was restored by addition of cAMP. In wild-type cells the non-metabolizable fructose analogue xylitol prevented fermentation of these sugars, confirming that the fructose PTS regulates cAMP levels. Development of competence under standard inducing conditions was reduced 250-fold by the ptsI mutation, unless cells were provided with exogenous cAMP. Competence is thus shown to be under direct nutritional control by a fructose-specific PTS.

摘要

细胞内cAMP浓度的变化在流感嗜血杆菌中发挥着重要作用,它既调节糖类利用,也调节自然转化的感受态。在肠道细菌中,cAMP水平受磷酸烯醇丙酮酸:葡萄糖磷酸转移酶系统(PTS)控制,以响应其所转运的首选糖类可用性的变化。我们通过多种方法证明了流感嗜血杆菌中存在一种简单的PTS。我们克隆了编码PTS酶I的流感嗜血杆菌ptsI基因;基因组分析将其定位在一个与肠道细菌的pts操纵子结构同源的pts操纵子中。体外磷酸化试验证实了功能性PTS成分的存在。ptsI基因敲除突变使果糖摄取量降至野生型速率的1%,即使提供外源性cAMP也会消除果糖发酵。ptsI突变还阻止了核糖和半乳糖的发酵,但通过添加cAMP可恢复对这些cAMP依赖性糖类的利用。在野生型细胞中,不可代谢的果糖类似物木糖醇阻止了这些糖类的发酵,证实果糖PTS调节cAMP水平。除非为细胞提供外源性cAMP,否则ptsI突变会使标准诱导条件下感受态的发育降低250倍。因此,感受态显示受果糖特异性PTS的直接营养控制。

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