Engineering an Optogenetic CRISPRi Platform for Improved Chemical Production

被引:35
|
作者
Wu, Peiling [1 ]
Chen, Yufen [1 ]
Liu, Mingyu [1 ]
Xiao, Gezhi [1 ]
Yuan, Jifeng [1 ]
机构
[1] Xiamen Univ, Innovat Ctr Cell Signaling Network, State Key Lab Cellular Stress Biol, Sch Life Sci, Xiamen 361102, Fujian, Peoples R China
来源
ACS SYNTHETIC BIOLOGY | 2021年 / 10卷 / 01期
关键词
optogenetic CRISPRi; EL222; dynamic regulation; resource allocation; muconic acid; GENE-EXPRESSION; PHOSPHOENOLPYRUVATE CARBOXYLASE; MEVALONATE PATHWAY; DYNAMIC REGULATION; METABOLIC FLUXES; DNA-BINDING; RNA; OPTIMIZATION; DIMERIZATION; BACTERIA;
D O I
10.1021/acssynbio.0c00488
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Microbial synthesis of chemicals typically requires the redistribution of metabolic flux toward the synthesis of targeted products. Dynamic control is emerging as an effective approach for solving the hurdles mentioned above. As light could control the cell behavior in a spatial and temporal manner, the optogeneticCRISPR interference (opto-CRISPRi) technique that allocates the metabolic resources according to different optical signal frequencies will enable bacteria to be controlled between the growth phase and the production stage. In this study, we applied a blue light-sensitive protein EL222 to regulate the expression of the dCpf1-mediated CRISPRi system that turns off the competitive pathways and redirects the metabolic flux toward the heterologous muconic acid synthesis in Escherichia coli. We found that the opto-CRISPRi system dynamically regulating the suppression of the central metabolism and competitive pathways could increase the muconic acid production by 130%. These results demonstrated that the opto-CRISPRi platform is an effective method for enhancing chemical synthesis with broad utilities.
引用
收藏
页码:125 / 131
页数:7
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