Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL, 60208, USA; Center for Synthetic Biology, Northwestern University, Evanston, IL, 60208, USA; Chemistry of Life Processes Institute, Northwestern University, Evanston, IL, 60208, USA.
Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL, 60208, USA.
Metab Eng. 2023 Mar;76:133-145. doi: 10.1016/j.ymben.2023.01.009. Epub 2023 Jan 29.
Cell-free systems are useful tools for prototyping metabolic pathways and optimizing the production of various bioproducts. Mechanistically-based kinetic models are uniquely suited to analyze dynamic experimental data collected from cell-free systems and provide vital qualitative insight. However, to date, dynamic kinetic models have not been applied with rigorous biological constraints or trained on adequate experimental data to the degree that they would give high confidence in predictions and broadly demonstrate the potential for widespread use of such kinetic models. In this work, we construct a large-scale dynamic model of cell-free metabolism with the goal of understanding and optimizing butanol production in a cell-free system. Using a combination of parameterization methods, the resultant model captures experimental metabolite measurements across two experimental conditions for nine metabolites at timepoints between 0 and 24 h. We present analysis of the model predictions, provide recommendations for butanol optimization, and identify the aldehyde/alcohol dehydrogenase as the primary bottleneck in butanol production. Sensitivity analysis further reveals the extent to which various parameters are constrained, and our approach for probing valid parameter ranges can be applied to other modeling efforts.
无细胞系统是用于对代谢途径进行原型设计和优化各种生物制品生产的有用工具。基于机制的动力学模型非常适合分析从无细胞系统收集的动态实验数据,并提供重要的定性见解。然而,迄今为止,动态动力学模型尚未应用严格的生物学约束条件,也没有用足够的实验数据进行训练,以至于无法对预测结果充满信心,也无法广泛展示此类动力学模型的广泛应用潜力。在这项工作中,我们构建了一个大规模的无细胞代谢动力学模型,旨在理解和优化无细胞系统中的丁醇生产。使用参数化方法的组合,该模型在两个实验条件下捕获了九个代谢物在 0 到 24 小时之间的 24 个时间点的实验代谢物测量值。我们展示了对模型预测的分析,提供了丁醇优化的建议,并确定醛/醇脱氢酶是丁醇生产的主要瓶颈。敏感性分析进一步揭示了各种参数受到约束的程度,我们用于探测有效参数范围的方法可应用于其他建模工作。