Systems metabolic engineering: Genome-scale models and beyond

被引:90
作者
Blazeck, John [1 ]
Alper, Hal [1 ]
机构
[1] Univ Texas Austin, Dept Chem Engn, Austin, TX 78712 USA
关键词
Genome-scale modeling; Metabolic engineering; Systems biology; IMPROVED ETHANOL TOLERANCE; ESCHERICHIA-COLI; SACCHAROMYCES-CEREVISIAE; TRANSCRIPTIONAL REGULATION; LYCOPENE BIOSYNTHESIS; MICROBIAL-PRODUCTION; BIOCYC COLLECTION; DATABASE; RECONSTRUCTION; SEQUENCE;
D O I
10.1002/biot.200900247
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The advent of high throughput genome-scale bioinformatics has led to an exponential increase in available cellular system data. Systems metabolic engineering attempts to use data-driven approaches based on the data collected with high throughput technologies to identify gene targets and optimize phenotypical properties on a systems level. Current systems metabolic engineering tools are limited for predicting and defining complex phenotypes such as chemical tolerances and other global, multigenic traits. The most pragmatic systems-based tool for metabolic engineering to arise is the in silico genome-scale metabolic reconstruction. This tool has seen wide adoption for modeling cell growth and predicting beneficial gene knockouts, and we examine here how this approach can be expanded for novel organisms. This review will highlight advances of the systems metabolic engineering approach with a focus on de novo development and use of genome-scale metabolic reconstructions for metabolic engineering applications. We will then discuss the challenges and prospects for this emerging field to enable model-based metabolic engineering. Specifically, we argue that current state-of-the-art systems metabolic engineering techniques represent a viable first step for improving product yield that still must be followed by combinatorial techniques or random strain mutagenesis to achieve optimal cellular systems.
引用
收藏
页码:647 / 659
页数:13
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