Dromms Robert A, Styczynski Mark P
School of Chemical & Biomolecular Engineering, Georgia Institute of Technology, 311 Ferst Drive NW, Atlanta, GA 30332, USA.
Metabolites. 2012 Dec 14;2(4):1090-122. doi: 10.3390/metabo2041090.
The goals of metabolic engineering are well-served by the biological information provided by metabolomics: information on how the cell is currently using its biochemical resources is perhaps one of the best ways to inform strategies to engineer a cell to produce a target compound. Using the analysis of extracellular or intracellular levels of the target compound (or a few closely related molecules) to drive metabolic engineering is quite common. However, there is surprisingly little systematic use of metabolomics datasets, which simultaneously measure hundreds of metabolites rather than just a few, for that same purpose. Here, we review the most common systematic approaches to integrating metabolite data with metabolic engineering, with emphasis on existing efforts to use whole-metabolome datasets. We then review some of the most common approaches for computational modeling of cell-wide metabolism, including constraint-based models, and discuss current computational approaches that explicitly use metabolomics data. We conclude with discussion of the broader potential of computational approaches that systematically use metabolomics data to drive metabolic engineering.
关于细胞当前如何利用其生化资源的信息,可能是为设计细胞生产目标化合物的策略提供依据的最佳方式之一。利用对目标化合物(或一些密切相关分子)的细胞外或细胞内水平分析来推动代谢工程是相当常见的。然而,令人惊讶的是,为了同样的目的,很少有系统地使用代谢组学数据集的情况,代谢组学数据集能同时测量数百种代谢物,而不仅仅是少数几种。在这里,我们回顾了将代谢物数据与代谢工程相结合的最常见系统方法,重点是使用全代谢组数据集的现有工作。然后,我们回顾了一些用于全细胞代谢计算建模的最常见方法,包括基于约束的模型,并讨论了当前明确使用代谢组学数据的计算方法。我们最后讨论了系统使用代谢组学数据来推动代谢工程的计算方法的更广泛潜力。