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基于13C标记实验以及酶活性测定和细胞内代谢物测量的ppc突变型大肠杆菌的代谢通量分析。

Metabolic flux analysis for a ppc mutant Escherichia coli based on 13C-labelling experiments together with enzyme activity assays and intracellular metabolite measurements.

作者信息

Peng Lifeng, Arauzo-Bravo Marcos J, Shimizu Kazuyuki

机构信息

Department of Biochemical Engineering and Science, Kyushu Institute of Technology, Iizuka, Fukuoka 820-8502, Japan.

出版信息

FEMS Microbiol Lett. 2004 Jun 1;235(1):17-23. doi: 10.1016/j.femsle.2004.04.003.

Abstract

The physiology and central metabolism of a ppc mutant Escherichia coli were investigated based on the metabolic flux distribution obtained by (13)C-labelling experiments using gas chromatography-mass spectrometry (GC-MS) and 2-dimensional nuclear magnetic resonance (2D NMR) strategies together with enzyme activity assays and intracellular metabolite concentration measurements. Compared to the wild type, its ppc mutant excreted little acetate and produced less carbon dioxide at the expense of a slower growth rate and a lower glucose uptake rate. Consequently, an improvement of the biomass yield on glucose was observed in the ppc mutant. Enzyme activity measurements revealed that isocitrate lyase activity increased by more than 3-fold in the ppc mutant. Some TCA cycle enzymes such as citrate synthase, aconitase and malate dehydrogenase were also upregulated, but enzymes of glycolysis and the pentose phosphate pathway were downregulated. The intracellular intermediates in the glycolysis and the pentose phosphate pathway, therefore, accumulated, while acetyl coenzyme A and oxaloacetate concentrations decreased in the ppc mutant. The intracellular metabolic flux analysis uncovered that deletion of ppc resulted in the appearance of the glyoxylate shunt, with 18.9% of the carbon flux being channeled via the glyoxylate shunt. However, the flux of the pentose phosphate pathway significantly decreased in the ppc mutant.

摘要

基于气相色谱-质谱联用(GC-MS)和二维核磁共振(2D NMR)技术的¹³C标记实验所获得的代谢通量分布,结合酶活性测定和细胞内代谢物浓度测量,对ppc突变型大肠杆菌的生理学和中心代谢进行了研究。与野生型相比,其ppc突变体分泌的乙酸很少,产生的二氧化碳也较少,但生长速率较慢且葡萄糖摄取率较低。因此,在ppc突变体中观察到葡萄糖生物量产量有所提高。酶活性测量结果显示,ppc突变体中异柠檬酸裂解酶活性增加了3倍以上。一些三羧酸循环酶,如柠檬酸合酶、乌头酸酶和苹果酸脱氢酶也上调,但糖酵解和磷酸戊糖途径的酶下调。因此,ppc突变体中糖酵解和磷酸戊糖途径的细胞内中间产物积累,而乙酰辅酶A和草酰乙酸浓度降低。细胞内代谢通量分析发现,ppc的缺失导致乙醛酸循环支路的出现,18.9%的碳通量通过乙醛酸循环支路。然而,ppc突变体中磷酸戊糖途径的通量显著降低。

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