Kerkhoven Eduard J, Lahtvee Petri-Jaan, Nielsen Jens
Department of Chemical and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
Novo Nordisk Foundation Center for Biosustainability, Chalmers University of Technology, Gothenburg, Sweden.
FEMS Yeast Res. 2015 Feb;15(1):1-13. doi: 10.1111/1567-1364.12199. Epub 2015 Jan 14.
Generally, a microorganism's phenotype can be described by its pattern of metabolic fluxes. Although fluxes cannot be measured directly, inference of fluxes is well established. In biotechnology the aim is often to increase the capacity of specific fluxes. For this, metabolic engineering methods have been developed and applied extensively. Many of these rely on balancing of intracellular metabolites, redox, and energy fluxes, using genome-scale models (GEMs) that in combination with appropriate objective functions and constraints can be used to predict potential gene targets for obtaining a preferred flux distribution. These methods point to strategies for altering gene expression; however, fluxes are often controlled by post-transcriptional events. Moreover, GEMs are usually not taking into account metabolic regulation, thermodynamics and enzyme kinetics. To facilitate metabolic engineering, tools from synthetic biology have emerged, enabling integration and assembly of naturally nonexistent, but well-characterized components into a living organism. To describe these systems kinetic models are often used and to integrate these systems with the standard metabolic engineering approach, it is necessary to expand the modeling of metabolism to consider kinetics of individual processes. This review will give an overview about models available for metabolic engineering of yeast and discusses their applications.
一般来说,微生物的表型可以通过其代谢通量模式来描述。虽然通量无法直接测量,但通量的推断已经很成熟。在生物技术领域,目标通常是提高特定通量的能力。为此,代谢工程方法已经得到广泛开发和应用。其中许多方法依赖于利用基因组规模模型(GEMs)平衡细胞内代谢物、氧化还原和能量通量,这些模型与适当的目标函数和约束条件相结合,可用于预测获得优选通量分布的潜在基因靶点。这些方法指出了改变基因表达的策略;然而,通量往往受转录后事件控制。此外,GEMs通常没有考虑代谢调节、热力学和酶动力学。为了促进代谢工程,合成生物学工具应运而生,能够将天然不存在但特征明确的组件整合和组装到活生物体中。为了描述这些系统,经常使用动力学模型,为了将这些系统与标准代谢工程方法相结合,有必要扩展代谢建模以考虑单个过程的动力学。本综述将概述可用于酵母代谢工程的模型,并讨论它们的应用。