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转录后调控系统CSR控制大肠杆菌上糖酵解中代谢池的平衡。

The post-transcriptional regulatory system CSR controls the balance of metabolic pools in upper glycolysis of Escherichia coli.

作者信息

Morin Manon, Ropers Delphine, Letisse Fabien, Laguerre Sandrine, Portais Jean-Charles, Cocaign-Bousquet Muriel, Enjalbert Brice

机构信息

Université de Toulouse; INSA, UPS, INP, 135 Avenue de Rangueil, F-31077, Toulouse, France.

INRA, UMR792 Ingénierie des Systèmes Biologiques et des Procédés, LISBP, F-31400, Toulouse, France.

出版信息

Mol Microbiol. 2016 May;100(4):686-700. doi: 10.1111/mmi.13343. Epub 2016 Feb 26.

Abstract

Metabolic control in Escherichia coli is a complex process involving multilevel regulatory systems but the involvement of post-transcriptional regulation is uncertain. The post-transcriptional factor CsrA is stated as being the only regulator essential for the use of glycolytic substrates. A dozen enzymes in the central carbon metabolism (CCM) have been reported as potentially controlled by CsrA, but its impact on the CCM functioning has not been demonstrated. Here, a multiscale analysis was performed in a wild-type strain and its isogenic mutant attenuated for CsrA (including growth parameters, gene expression levels, metabolite pools, abundance of enzymes and fluxes). Data integration and regulation analysis showed a coordinated control of the expression of glycolytic enzymes. This also revealed the imbalance of metabolite pools in the csrA mutant upper glycolysis, before the phosphofructokinase PfkA step. This imbalance is associated with a glucose-phosphate stress. Restoring PfkA activity in the csrA mutant strain suppressed this stress and increased the mutant growth rate on glucose. Thus, the carbon storage regulator system is essential for the effective functioning of the upper glycolysis mainly through its control of PfkA. This work demonstrates the pivotal role of post-transcriptional regulation to shape the carbon metabolism.

摘要

大肠杆菌中的代谢控制是一个复杂的过程,涉及多级调节系统,但转录后调节的参与情况尚不确定。转录后因子CsrA被认为是利用糖酵解底物所必需的唯一调节因子。据报道,中心碳代谢(CCM)中的十几种酶可能受CsrA调控,但其对CCM功能的影响尚未得到证实。在此,我们对野生型菌株及其CsrA减毒的同基因突变体进行了多尺度分析(包括生长参数、基因表达水平、代谢物库、酶丰度和通量)。数据整合和调节分析表明糖酵解酶的表达受到协同控制。这还揭示了csrA突变体上糖酵解中代谢物库在磷酸果糖激酶PfkA步骤之前的失衡。这种失衡与磷酸葡萄糖应激有关。在csrA突变体菌株中恢复PfkA活性可抑制这种应激并提高突变体在葡萄糖上的生长速率。因此,碳储存调节系统对于上糖酵解的有效运作至关重要,主要是通过其对PfkA的控制。这项工作证明了转录后调节在塑造碳代谢中的关键作用。

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