首页> 外文期刊>Biochemical Engineering Journal >Effect of sucA or sucC gene knockout on the metabolism in Escherichia coli based on gene expressions,enzyme activities,intracellular metabolite concentrations and metabolic fluxes by ~(13)C-labeling experiments
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Effect of sucA or sucC gene knockout on the metabolism in Escherichia coli based on gene expressions,enzyme activities,intracellular metabolite concentrations and metabolic fluxes by ~(13)C-labeling experiments

机译:基于(13)C标记实验的基因表达,酶活性,细胞内代谢物浓度和代谢通量,sucA或sucC基因敲除对大肠杆菌代谢的影响

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The effect of sucA or sucC gene knockout on the metabolism in Escherichia coli was investigated for the aerobic cell growth in batch and continuous cultivations based on gene expressions,enzyme activities,intracellular metabolite concentrations and metabolic flux analysis.In the batch cultivation,the cell growth rate and the glucose uptake rate were lower for sucA mutant as compared with the parent strain,while it was not the case for sucC mutant.A significantly higher amount of acetate was produced,and it was not utilized in sucC mutant,while a little less acetate was produced in sucA mutant as compared with the parent strain.Unlike the parent strain and sucC mutant,sucA mutant excreted a little amount of L-glutamate.Enzyme activity results show that some of the glycolytic enzymes such as Tpi and Pgk were up-regulated,while Pfk,Fba and Pyk activities were down-regulated for sucA mutant as compared with the parent strain.For sucC mutant,the activities of Pfk,Fba,Tpi,GAPDH,Pgk and Pyk activities were down-regulated.As for the TCA cycle enzymes,the activities of CS and ICDH were down-regulated,while those of Icl,MS,Fum and MDH were up-regulated for sucA mutant.The activities of the oxidative pentose phosphate (PP)pathway enzymes such as G6PDH and 6PGDH and the gluconeogenic pathway enzyme such as Mez were up-regulated in sucA mutant.The Ack activity was down-regulated for sucA mutant,but not for sucC mutant.In continuous cultivation,the gene expression results indicate that the global regulatory genes such as fadR and iclR were slightly down-regulated in sucA mutant,which enhanced the expression of aceA gene and caused the up-regulation of the isocitrate lyase activity in sucA mutant,while fadR and iclR of sucC mutant changed little and no isocitrate lyase activation was observed for sucC mutant.Some other global regulatory genes such as arcA and fnr genes were down-regulated in both mutants,which caused some of the TCA cycle genes to be up-regulated.The effect of the sucA gene knockout on the metabolic flux distributions was investigated based on ~1H-~(13)C NMR spectra and GC-MS signals obtained from ~(13)C-labeling experiments.Flux analysis results indicate that the knockout of sucA gene caused the activation of PP pathway and the glyoxylate shunt.The fluxes through glycolysis and the TCA cycle were down-regulated in the sucA mutant.On the other hand,the fluxes through PP pathway and the anaplerotic reactions of Ppc-Pck and Mez increased.
机译:基于基因表达,酶活性,细胞内代谢产物浓度和代谢通量分析,研究了sucA或sucC基因敲除对大肠杆菌中分批和连续培养需氧细胞生长的影响。分批培养中,细胞生长与亲本菌株相比,sucA突变体的葡萄糖吸收率和葡萄糖吸收率较低,而sucC突变体则不是这样。产生的乙酸盐量明显更高,并且不用于sucC突变体,而少得多与亲本菌株相比,sucA突变体产生了乙酸盐。与亲本菌株和sucC突变体不同,sucA突变体分泌了少量的L-谷氨酸。酶活性结果表明,某些糖酵解酶(例如Tpi和Pgk)- sucA突变体与亲本菌株相比,Pfk,Fba和Pyk活性被下调。对于sucC突变体,sfA,Pba,Tpi,GAPDH,Pgk和Pyk a的活性被降低。 sucA突变体的TCA循环酶,CS和ICDH的活性均被下调,而Icl,MS,Fum和MDH的活性均被上调。在sucA突变体中,G6PDH和6PGDH等PP)途径酶和Mez等糖异生途径酶被上调.sucA突变体的Ack活性被下调,而sucC突变体的Ack活性却被下调。在连续培养中,基因表达结果表明sucA突变体中的全球调控基因fadR和iclR均被轻微下调,这增强了aceA基因的表达并导致sucA突变体中异柠檬酸裂合酶活性的上调,而sucC突变体的fadR和iclR发生了变化。 sucC突变体几乎没有观察到异柠檬酸裂合酶活化。在这两个突变体中,其他一些全局调控基因(例如arcA和fnr基因)均被下调,这导致一些TCA循环基因被上调。根据〜1H-〜(13)C NMR谱图和〜(13)C标记实验获得的GC-MS信号,研究了sucA基因在代谢通量分布上的敲除现象。通量分析结果表明sucA基因的敲除引起了代谢的变化。 sucA突变体中通过糖酵解和TCA循环的通量被下调。另一方面,通过PP通路的通量以及Ppc-Pck和Mez的动脉粥样硬化反应增加。

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