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Application of dynamic metabolic flux analysis for process modeling: Robust flux estimation with regularization confidence bounds and selection of elementary modes

机译:动态代谢通量分析在过程建模中的应用:具有正则化置信界和基本模式选择的鲁棒通量估计

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摘要

In macroscopic dynamic models of fermentation processes, elementary modes (EM) derived from metabolic networks are often used to describe the reaction stoichiometry in a simplified manner and to build predictive models by parameterizing kinetic rate equations for the EM. In this procedure, the selection of a set of EM is a key step which is followed by an estimation of their reaction rates and of the associated confidence bounds. In this paper, we present a method for the computation of reaction rates of cellular reactions and EM as well as an algorithm for the selection of EM for process modeling. The method is based on the dynamic metabolic flux analysis (DMFA) proposed by Leighty and Antoniewicz (2011, , 13(6), 745–755) with additional constraints, regularization and analysis of uncertainty. Instead of using estimated uptake or secretion rates, concentration measurements are used directly to avoid an amplification of measurement errors by numerical differentiation. It is shown that the regularized DMFA for EM method is significantly more robust against measurement noise than methods using estimated rates. The confidence intervals for the estimated reaction rates are obtained by bootstrapping. For the selection of a set of EM for a given st oichiometric model, the DMFA for EM method is combined with a multiobjective genetic algorithm. The method is applied to real data from a CHO fed‐batch process. From measurements of six fed‐batch experiments, 10 EM were identified as the smallest subset of EM based upon which the data can be described sufficiently accurately by a dynamic model. The estimated EM reaction rates and their confidence intervals at different process conditions provide useful information for the kinetic modeling and subsequent process optimization.
机译:在发酵过程的宏观动态模型中,通常使用源自代谢网络的基本模式(EM)以简化的方式描述反应化学计量,并通过对EM的动力学速率方程进行参数化来建立预测模型。在此过程中,选择一组EM是关键步骤,然后估算它们的反应速率和相关的置信范围。在本文中,我们提出了一种计算细胞反应和EM反应速率的方法,以及一种用于过程建模的EM选择算法。该方法基于Leighty和Antoniewicz(2011,,13(6),745-755)提出的动态代谢通量分析(DMFA),并具有其他约束,正则化和不确定性分析。代替使用估计的摄取或分泌速率,浓度测量直接用于避免由于数值微分而导致的测量误差的放大。结果表明,用于EM方法的正规化DMFA比使用估计速率的方法对测量噪声的鲁棒性更高。通过自举获得估计反应速率的置信区间。为了为给定的化学计量模型选择一组EM,将EM方法的DMFA与多目标遗传算法结合使用。该方法适用于CHO批处理的真实数据。通过对六个分批补料实验的测量,确定了10个EM是EM的最小子集,基于该子集,可以通过动态模型足够准确地描述数据。估计的EM反应速率及其在不同工艺条件下的置信区间为动力学建模和后续工艺优化提供了有用的信息。

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