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Predicting microbial growth kinetics with the use of genetic circuit models

机译:使用遗传回路模型预测微生物生长动力学

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A novel modeling approach for the description of bioprocesses is proposed, linking microbial growth kinetics to gene regulation. An example is given with the development and experimental validation of a dynamic mathematical model of the TOL plasmid of Pseudomonas putida mt-2, which is used for the metabolism of m-xylene. The model of this genetic circuit is coupled to a growth kinetic model through predictions of rate-limiting enzyme concentrations that control biomass growth and substrate consumption. Batch cultures of mt-2 fed with m-xylene were performed to estimate model parameters and to confirm that the combined model successfully describes the bioprocess, through mRNA, biomass and m-xylene concentration measurements. However, mathematical models developed exclusively based on macroscopic measurements failed to predict the process variables, highlighting the importance of gene regulation for the development of advanced biological models.
机译:提出了一种描述生物过程的新颖建模方法,将微生物生长动力学与基因调控联系起来。举例说明恶臭假单胞菌mt-2 TOL质粒的动态数学模型的开发和实验验证,该模型用于间二甲苯的代谢。通过预测控制生物量生长和底物消耗的限速酶浓度,该遗传回路的模型与生长动力学模型耦合。进行了以间二甲苯喂养的mt-2的分批培养,以估计模型参数并通过mRNA,生物量和间二甲苯浓度测量来确认组合模型成功地描述了生物过程。但是,仅基于宏观测量结果开发的数学模型无法预测过程变量,从而突出了基因调控对高级生物学模型发展的重要性。

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