Application of different types of CRISPR/Cas-based systems in bacteria.


Journal

Microbial cell factories
ISSN: 1475-2859
Titre abrégé: Microb Cell Fact
Pays: England
ID NLM: 101139812

Informations de publication

Date de publication:
03 Sep 2020
Historique:
received: 14 06 2020
accepted: 25 08 2020
entrez: 5 9 2020
pubmed: 5 9 2020
medline: 5 6 2021
Statut: epublish

Résumé

As important genome editing tools, CRISPR/Cas systems, especially those based on type II Cas9 and type V Cas12a, are widely used in genetic and metabolic engineering of bacteria. However, the intrinsic toxicity of Cas9 and Cas12a-mediated CRISPR/Cas tools can lead to cell death in some strains, which led to the development of endogenous type I and III CRISPR/Cas systems. However, these systems are hindered by complicated development and limited applications. Thus, further development and optimization of CRISPR/Cas systems is needed. Here, we briefly summarize the mechanisms of different types of CRISPR/Cas systems as genetic manipulation tools and compare their features to provide a reference for selecting different CRISPR/Cas tools. Then, we show the use of CRISPR/Cas technology for bacterial strain evolution and metabolic engineering, including genome editing, gene expression regulation and the base editor tool. Finally, we offer a view of future directions for bacterial CRISPR/Cas technology.

Identifiants

pubmed: 32883277
doi: 10.1186/s12934-020-01431-z
pii: 10.1186/s12934-020-01431-z
pmc: PMC7470686
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

172

Subventions

Organisme : National Natural Science Foundation of China
ID : NSFC 31800086

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Auteurs

Zhenquan Liu (Z)

School of Biological Engineering, Dalian Polytechnic University, Dalian, 116034, People's Republic of China.
Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, 300308, China.
Key Laboratory of Systems Microbial Biotechnology, Chinese Academy of Sciences, Tianjin, 300308, People's Republic of China.

Huina Dong (H)

Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, 300308, China.
Key Laboratory of Systems Microbial Biotechnology, Chinese Academy of Sciences, Tianjin, 300308, People's Republic of China.

Yali Cui (Y)

Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, 300308, China.
Key Laboratory of Systems Microbial Biotechnology, Chinese Academy of Sciences, Tianjin, 300308, People's Republic of China.

Lina Cong (L)

School of Biological Engineering, Dalian Polytechnic University, Dalian, 116034, People's Republic of China. linacong@163.com.

Dawei Zhang (D)

Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, 300308, China. zhang_dw@tib.cas.cn.
Key Laboratory of Systems Microbial Biotechnology, Chinese Academy of Sciences, Tianjin, 300308, People's Republic of China. zhang_dw@tib.cas.cn.
University of Chinese Academy of Sciences, Beijing, 100049, China. zhang_dw@tib.cas.cn.

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