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Kinetic modelling of the Zymomonas mobilis Entner–Doudoroff pathway: insights into control and functionality

机译:Zymomonas Mobilis Entner-Doudoroff路径的动力学建模:控制和功能的见解

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Zymomonas mobilis, an ethanol-producing bacterium, possesses the Entner–Doudoroff (E-D) pathway, pyruvate decarboxylase and two alcohol dehydrogenase isoenzymes for the fermentative production of ethanol and carbon dioxide from glucose. Using available kinetic parameters, we have developed a kinetic model that incorporates the enzymic reactions of the E-D pathway, both alcohol dehydrogenases, transport reactions and reactions related to ATP metabolism. After optimizing the reaction parameters within likely physiological limits, the resulting kinetic model was capable of simulating glycolysis in vivo and in cell-free extracts with good agreement with the fluxes and steady-state intermediate concentrations reported in previous experimental studies. In addition, the model is shown to be consistent with experimental results for the coupled response of ATP concentration and glycolytic flux to ATPase inhibition. Metabolic control analysis of the model revealed that the majority of flux control resides not inside, but outside the E-D pathway itself, predominantly in ATP consumption, demonstrating why past attempts to increase the glycolytic flux through overexpression of glycolytic enzymes have been unsuccessful. Co-response analysis indicates how homeostasis of ATP concentrations starts to deteriorate markedly at the highest glycolytic rates. This kinetic model has potential for application in Z. mobilis metabolic engineering and, since there are currently no E-D pathway models available in public databases, it can serve as a basis for the development of models for other micro-organisms possessing this type of glycolytic pathway.
机译:Zymomonas Mobilis是一种乙醇生产细菌,具有Entner-Doudoroff(E-D)途径,丙酮酸脱羧酶和两种醇脱氢酶同工酶,用于从葡萄糖中发酵产生乙醇和二氧化碳。使用可用的动力学参数,我们开发了一种动力学模型,其含有E-D途径,醇脱氢酶,转运反应和与ATP代谢相关的反应的酶反应。在优化在可能的生理限制中的反应参数之后,所得到的动力学模型能够在体内和无细胞提取物中模拟糖醇分解,与先前的实验研究中报道的助液和稳态中间浓度良好。此外,该模型被证明与ATP浓度和糖酵解通量与ATP酶抑制的偶联响应的实验结果一致。该模型的代谢控制分析显示,大多数磁通控制不包括在内,但在E-D途径本身之外,主要是在ATP消费中,证明过去通过过表达通过过表达增加糖酵解酶的糖浆通量的原因是不成功的。共响应分析表明ATP浓度的稳态如何以最高的糖酵解率显着恶化。该动力学模型具有Z.Mobilis代谢工程的应用潜力,并且由于目前没有公共数据库中提供的ED途径型号,它可以作为具有这种具有这种具有这种类型的糖酵解途径的其他微生物的模型的基础。

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