Kim Jin Il, Varner Jeffery D, Ramkrishna Doraiswami
Forney Hall of Chemical Engineering, Purdue University, West Lafayette, IN 47907, USA.
Biotechnol Prog. 2008 Sep-Oct;24(5):993-1006. doi: 10.1002/btpr.73.
Flux balance analysis (FBA) in combination with the decomposition of metabolic networks into elementary modes has provided a route to modeling cellular metabolism. It is dependent, however, on the availability of external fluxes such as substrate uptake or growth rate before estimates can become available of intracellular fluxes. The framework classically does not allow modeling of metabolic regulation or the formulation of dynamic models except through dynamic measurement of external fluxes. The cybernetic modeling approach of Ramkrishna and coworkers provides a dynamic framework for modeling metabolic systems because of its focus on describing regulatory processes based on cybernetic arguments and hence has the capacity to describe both external and internal fluxes. In this article, we explore the alternative of developing hybrid models combining cybernetic models for the external fluxes with the flux balance approach for estimation of the internal fluxes. The approach has the merit of the simplicity of the early cybernetic models and hence computationally facile while also providing detailed information on intracellular fluxes. The hybrid model of this article is based on elementary mode decomposition of the metabolic network. The uptake rates for the various elementary modes are combined using global cybernetic variables based on maximizing substrate uptake rates. Estimation of intracellular metabolism is based on its stoichiometric coupling with the external fluxes under the assumption of (pseudo-) steady state conditions. The set of parameters of the hybrid model was estimated with the aid of nonlinear optimization routine, by fitting simulations with dynamic experimental data on concentrations of biomass, substrate, and fermentation products. The hybrid model estimations were tested with FBA (based on measured substrate uptake rate) for two different metabolic networks (one is a reduced network which fixes ATP contribution to the biomass and maintenance requirement of ATP, and the other network is a more complex network which has a separate reaction for maintenance.) for the same experiment involving anaerobic growth of E. coli GJT001. The hybrid model estimated glucose consumption and all fermentation byproducts to better than 10%. The FBA makes similar estimations of fermentation products, however, with the exception of succinate. The simulation results show that the global cybernetic variables alone can regulate the metabolic reactions obtaining a very satisfactory fit to the measured fermentation byproducts. In view of the hybrid model's ability to predict biomass growth and fermentation byproducts of anaerobic E. coli GJT001, this reduced order model offers a computationally efficient alternative to more detailed models of metabolism and hence useful for the simulation of bioreactors.
通量平衡分析(FBA)与将代谢网络分解为基本模式相结合,为细胞代谢建模提供了一条途径。然而,它依赖于外部通量的可用性,例如在能够估计细胞内通量之前的底物摄取或生长速率。经典的框架不允许对代谢调节进行建模,也不允许构建动态模型,除非通过外部通量的动态测量。Ramkrishna及其同事的控制论建模方法为代谢系统建模提供了一个动态框架,因为它专注于基于控制论观点描述调节过程,因此有能力描述外部和内部通量。在本文中,我们探索了开发混合模型的另一种方法,即将用于外部通量的控制论模型与用于估计内部通量的通量平衡方法相结合。该方法具有早期控制论模型简单的优点,因此计算简便,同时还能提供有关细胞内通量的详细信息。本文的混合模型基于代谢网络的基本模式分解。基于最大化底物摄取速率,使用全局控制论变量组合各种基本模式的摄取速率。细胞内代谢的估计基于在(伪)稳态条件假设下其与外部通量的化学计量耦合。借助非线性优化程序,通过将模拟结果与关于生物量、底物和发酵产物浓度的动态实验数据进行拟合,估计了混合模型的参数集。对于涉及大肠杆菌GJT001厌氧生长的同一实验,使用FBA(基于测量的底物摄取速率)对两个不同的代谢网络(一个是简化网络,固定了ATP对生物量的贡献以及ATP的维持需求,另一个网络更复杂,有一个单独的维持反应)测试了混合模型估计值。混合模型对葡萄糖消耗和所有发酵副产物的估计误差优于10%。FBA对发酵产物的估计也类似,不过琥珀酸除外。模拟结果表明,仅全局控制论变量就能调节代谢反应,从而非常令人满意地拟合测量的发酵副产物。鉴于混合模型能够预测厌氧大肠杆菌GJT001的生物量生长和发酵副产物,这种降阶模型为更详细的代谢模型提供了一种计算高效的替代方案,因此对于生物反应器的模拟很有用。