Recent advances in high-throughput metabolic engineering: Generation of oligonucleotide-mediated genetic libraries

被引:5
|
作者
Li, Ye [1 ,2 ]
Mensah, Emmanuel Osei [1 ,2 ]
Fordjour, Eric [1 ,2 ]
Bai, Jing [3 ]
Yang, Yankun [1 ,2 ]
Bai, Zhonghu [1 ,2 ]
机构
[1] Jiangnan Univ, Natl Engn Res Ctr Cereal Fermentat & Food Biomanu, Wuxi 214122, Jiangsu, Peoples R China
[2] Jiangnan Univ, Sch Biotechnol, Wuxi 214122, Jiangsu, Peoples R China
[3] Suzhou Univ Sci & Technol, Sch Chem & Life Sci, Suzhou 215009, Peoples R China
关键词
Genetic library; Oligonucleotides; CRISPR/Cas; sRNA; RNAi; Recombineering; Metabolic engineering; High-throughput screening; ARTIFICIAL SMALL RNAS; BACTERIAL SMALL RNAS; ESCHERICHIA-COLI; SACCHAROMYCES-CEREVISIAE; SOLUBLE-RNA; HOMOLOGOUS RECOMBINATION; BACILLUS-SUBTILIS; CRISPR; DESIGN; DNA;
D O I
10.1016/j.biotechadv.2022.107970
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
The preparation of genetic libraries is an essential step to evolve microorganisms and study genotype-phenotype relationships by high-throughput screening/selection. As the large-scale synthesis of oligonucleotides becomes easy, cheap, and high-throughput, numerous novel strategies have been developed in recent years to construct high-quality oligo-mediated libraries, leveraging state-of-art molecular biology tools for genome editing and gene regulation. This review presents an overview of recent advances in creating and characterizing in vitro and in vivo genetic libraries, based on CRISPR/Cas, regulatory RNAs, and recombineering, primarily for Escherichia coli and Saccharomyces cerevisiae. These libraries' applications in high-throughput metabolic engineering, strain evolution and protein engineering are also discussed.
引用
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页数:20
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