Screening and modular design for metabolic pathway optimization

被引:22
作者
Boock, Jason T. [1 ]
Gupta, Apoorv [2 ]
Prather, Kristala L. J. [1 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02142 USA
[2] MIT, Dept Biol Engn, Cambridge, MA 02142 USA
基金
美国国家科学基金会;
关键词
FATTY-ACIDS PRODUCTION; ESCHERICHIA-COLI; SACCHAROMYCES-CEREVISIAE; E; COLI; MICROBIAL SYNTHESIS; BIOSYNTHESIS; CHEMICALS; ALCOHOLS; FUELS; STRAINS;
D O I
10.1016/j.copbio.2015.08.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Biological conversion of substrate sugars to a variety of products is an increasingly popular option for chemical transformation due to its high specificity and because of significant interest in the use of renewable feedstocks. However, pathway optimization through metabolic engineering is often needed to make such molecules economically at a relevant scale. Employing effective methods to search and narrow the immense pathway parameter space is essential to meet performance metrics such as high titer, yield and productivity with efficiency. This review focuses on two practices that increase the likelihood of finding a more advantageous pathway solution: implementing a screen to identify high producers and utilizing modular pathway design to streamline engineering efforts. While screens seek to couple product titer with a high-throughput measurement output, modular design aims to rationally construct pathways to allow parallel optimization of various units. Both of these methodologies have proven widely successful in metabolic engineering, with combinations of them resulting in synergistic enhancements to pathway optimization. This review will particularly highlight their utility for microbially derived acid and alcohol products, which are of interest as fuels and value added products.
引用
收藏
页码:189 / 198
页数:10
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