Into new territory: improved microbial synthesis through engineering of the essential metabolic network

被引:25
作者
Lynch, Michael D. [1 ]
机构
[1] Duke Univ, Pratt Sch Engn, Dept Biomed Engn, CIEMAS, Room 1427,101 Sci Dr,Campus Box 90281, Durham, NC 27708 USA
基金
美国国家科学基金会;
关键词
CENTRAL CARBON METABOLISM; SEQUENCE-SPECIFIC CONTROL; ESCHERICHIA-COLI; GENE-EXPRESSION; SACCHAROMYCES-CEREVISIAE; PROTEIN-DEGRADATION; DYNAMIC CONTROL; INTERFERENCE SYSTEM; TOGGLE SWITCH; CRISPR;
D O I
10.1016/j.copbio.2016.01.009
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Advances in synthetic biology and metabolic engineering offer the promise of next generation bioprocesses to produce numerous products including specialty and bulk chemicals and even biofuels sustainably from renewable feedstocks. A primary challenge is the optimization of product flux, within a much larger and complex metabolic network. While simple gene deletion methods can be used in the case of non-essential byproduct pathways, more sophisticated approaches are required when competitive fluxes are essential to host cellular functions. Engineering essential metabolic networks has been traditionally off-limits to metabolic engineers. Newer approaches to be reviewed include the rebalancing or rewiring of the metabolic network by tuning the levels of essential enzymes and the use of dynamic metabolic control strategies to conditionally reduce essential competitive fluxes.
引用
收藏
页码:106 / 111
页数:6
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