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多聚磷酸盐代谢对大肠杆菌磷酸盐饥饿应答的影响。

Effect of polyphosphate metabolism on the Escherichia coli phosphate-starvation response.

作者信息

Van Dien S J, Keasling J D

机构信息

Department of Chemical Engineering, University of California, Berkeley, California 94720-1462, USA.

出版信息

Biotechnol Prog. 1999 Jul-Aug;15(4):587-93. doi: 10.1021/bp990067u.

Abstract

A previously developed dynamic model of the Escherichia coli Pho regulon was extended to investigate the effect of polyphosphate synthesis and degradation on this control system. Differential equations for ATP and polyphosphate were formulated, and the model was applied to the growth of cells containing the ppk and ppx genes under control of separate, inducible promoters. In agreement with recent experimental observations, the degradation of polyphosphate by PPX during a period of phosphate limitation could repress the phosphate-starvation response. This is attributed to the release of phosphate from the cell into the periplasm, where it can be detected by the external phosphate sensor. A segregated model was then developed to account for differences in K(I), the dissociation constant for the repression complex, among cells of the population. Since K(I) is the key parameter in determining whether the Pho response is induced or repressed at a particular surface phosphate concentration, this permitted the induction of some cells while others remained repressed. The induction profiles resulting from the population-averaged values more closely matched experimental results than did those with the nonsegregated model.

摘要

一个先前开发的大肠杆菌Pho调节子动态模型得到扩展,以研究多聚磷酸盐合成与降解对该控制系统的影响。构建了ATP和多聚磷酸盐的微分方程,并将该模型应用于在单独的可诱导启动子控制下含有ppk和ppx基因的细胞生长。与最近的实验观察结果一致,在磷酸盐限制期间PPX对多聚磷酸盐的降解可抑制磷酸盐饥饿反应。这归因于磷酸盐从细胞释放到周质中,在那里它可以被外部磷酸盐传感器检测到。然后开发了一个分离模型来解释群体中细胞间抑制复合物解离常数K(I)的差异。由于K(I)是决定在特定表面磷酸盐浓度下Pho反应是被诱导还是被抑制的关键参数,这使得一些细胞被诱导而其他细胞仍被抑制。与非分离模型相比,由群体平均值得出的诱导曲线与实验结果更接近。

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