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Revealing the Biological Meaning of Alternative Optimal Solutions of an E. coli Core Model through a System Identification Based Framework

机译:揭示 E替代最佳解的生物学意义。通过基于系统识别的框架的大肠杆菌核心模型

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Genome-scale metabolic network models (GEMs) have been developed and applied successfully in many applications. Among different modeling approaches, flux balance analysis (FBA), a constraint-based method, has attracted significant interest due to its simplicity and effectiveness. Due to the inherent redundancies built into the metabolic network, alternative optimal solutions in general exist in the implementations of FBA. Although mathematical and geometrical meanings of the alternative optima are straightforward, their biological meaning has not been fully understood. In this work, with theE. colicore model as an example, we apply a system identification based framework that we previously developed for GEM analysis to reveal the biological meaning of the alternative optimal solutions to FBA. We show that for theE. colicore model, the alternative solutions are related to each other as different means to achieve the same redox balance, i.e., total NADPH.
机译:基因组规模的代谢网络模型(GEM)已开发并成功应用于许多应用中。在不同的建模方法中,基于约束的方法通量平衡分析(FBA)由于其简单性和有效性而引起了人们的极大兴趣。由于内置在代谢网络中的固有冗余,通常在FBA的实现中存在替代的最佳解决方案。尽管替代最优的数学和几何含义很简单,但是它们的生物学含义还没有被完全理解。在这项工作中,有了E。以colicore模型为例,我们采用了我们先前为GEM分析开发的基于系统识别的框架,以揭示FBA替代最佳解决方案的生物学意义。我们为E展示了这一点。大肠杆菌模型,替代解决方案彼此相关,因为获得相同氧化还原平衡(即总NADPH)的方式不同。

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