CRISPR genetic toolkits of classical food microorganisms: Current state and future prospects

被引:11
作者
Lv, Xueqin [1 ,2 ]
Li, Yang [1 ,2 ]
Xiu, Xiang [1 ,2 ]
Liao, Chao [1 ,2 ]
Xu, Yameng [1 ,2 ]
Liu, Yanfeng [1 ,2 ]
Li, Jianghua [1 ,2 ]
Du, Guocheng [1 ,2 ]
Liu, Long [1 ,2 ,3 ]
机构
[1] Jiangnan Univ, Minist Educ, Key Lab Carbohydrate Chem & Biotechnol, Wuxi 214122, Peoples R China
[2] Jiangnan Univ, Sci Ctr Future Foods, Wuxi 214122, Peoples R China
[3] Jiangnan Univ, Food Lab Zhongyuan, Wuxi 214122, Peoples R China
基金
中国国家自然科学基金;
关键词
CRISPR/Cas; Food microorganisms; Lactic acid bacteria; Corynebacterium glutamicum; Bacillus subtilis; Saccharomycescerevisiae. Gene editing; Genome reconstruction; Metabolic regulation; ESCHERICHIA-COLI; METABOLIC FLUX; HUGE PHAGES; GENOME; SYSTEM; TRANSCRIPTION; SEQUENCE; DESIGN;
D O I
10.1016/j.biotechadv.2023.108261
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Production of food-related products using microorganisms in an environmentally friendly manner is a crucial solution to global food safety and environmental pollution issues. Traditional microbial modification methods rely on artificial selection or natural mutations, which require time for repeated screening and reproduction, leading to unstable results. Therefore, it is imperative to develop rapid, efficient, and precise microbial modification technologies. This review summarizes recent advances in the construction of gene editing and metabolic regulation toolkits based on the clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPRassociated proteins (CRISPR-Cas) systems and their applications in reconstructing food microorganism metabolic networks. The development and application of gene editing toolkits from single-site gene editing to multi-site and genome-scale gene editing was also introduced. Moreover, it presented a detailed introduction to CRISPR interference, CRISPR activation, and logic circuit toolkits for metabolic network regulation. Moreover, the current challenges and future prospects for developing CRISPR genetic toolkits were also discussed.
引用
收藏
页数:16
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