Development and Applications of CRISPR/Cas9-Based Genome Editing in Lactobacillus
Lactobacillus, a genus of lactic acid bacteria, plays a crucial function in food production preservation, and probiotics. It is particularly important to develop new Lactobacillus strains with superior performance by gene editing. Currently, the identification of its functional genes and the mining...
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Veröffentlicht in: | International journal of molecular sciences 2022-11, Vol.23 (21), p.12852 |
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description | Lactobacillus, a genus of lactic acid bacteria, plays a crucial function in food production preservation, and probiotics. It is particularly important to develop new Lactobacillus strains with superior performance by gene editing. Currently, the identification of its functional genes and the mining of excellent functional genes mainly rely on the traditional gene homologous recombination technology. CRISPR/Cas9-based genome editing is a rapidly developing technology in recent years. It has been widely applied in mammalian cells, plants, yeast, and other eukaryotes, but less in prokaryotes, especially Lactobacillus. Compared with the traditional strain improvement methods, CRISPR/Cas9-based genome editing can greatly improve the accuracy of Lactobacillus target sites and achieve traceless genome modification. The strains obtained by this technology may even be more efficient than the traditional random mutation methods. This review examines the application and current issues of CRISPR/Cas9-based genome editing in Lactobacillus, as well as the development trend of CRISPR/Cas9-based genome editing in Lactobacillus. In addition, the fundamental mechanisms of CRISPR/Cas9-based genome editing are also presented and summarized. |
doi_str_mv | 10.3390/ijms232112852 |
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It is particularly important to develop new Lactobacillus strains with superior performance by gene editing. Currently, the identification of its functional genes and the mining of excellent functional genes mainly rely on the traditional gene homologous recombination technology. CRISPR/Cas9-based genome editing is a rapidly developing technology in recent years. It has been widely applied in mammalian cells, plants, yeast, and other eukaryotes, but less in prokaryotes, especially Lactobacillus. Compared with the traditional strain improvement methods, CRISPR/Cas9-based genome editing can greatly improve the accuracy of Lactobacillus target sites and achieve traceless genome modification. The strains obtained by this technology may even be more efficient than the traditional random mutation methods. This review examines the application and current issues of CRISPR/Cas9-based genome editing in Lactobacillus, as well as the development trend of CRISPR/Cas9-based genome editing in Lactobacillus. In addition, the fundamental mechanisms of CRISPR/Cas9-based genome editing are also presented and summarized.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms232112852</identifier><identifier>PMID: 36361647</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Acids ; Bacteria ; CRISPR ; Dairy products ; DNA repair ; Editing ; Efficiency ; Eukaryotes ; Food ; Genes ; Genetic engineering ; Genetic modification ; Genome editing ; Genomes ; Gram-positive bacteria ; Homologous recombination ; Lactic acid ; Lactic acid bacteria ; Lactobacillus ; Mammalian cells ; Mutation ; Plant cells ; Prebiotics ; Probiotics ; Prokaryotes ; Proteins ; Review ; Strains (organisms)</subject><ispartof>International journal of molecular sciences, 2022-11, Vol.23 (21), p.12852</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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It is particularly important to develop new Lactobacillus strains with superior performance by gene editing. Currently, the identification of its functional genes and the mining of excellent functional genes mainly rely on the traditional gene homologous recombination technology. CRISPR/Cas9-based genome editing is a rapidly developing technology in recent years. It has been widely applied in mammalian cells, plants, yeast, and other eukaryotes, but less in prokaryotes, especially Lactobacillus. Compared with the traditional strain improvement methods, CRISPR/Cas9-based genome editing can greatly improve the accuracy of Lactobacillus target sites and achieve traceless genome modification. The strains obtained by this technology may even be more efficient than the traditional random mutation methods. This review examines the application and current issues of CRISPR/Cas9-based genome editing in Lactobacillus, as well as the development trend of CRISPR/Cas9-based genome editing in Lactobacillus. In addition, the fundamental mechanisms of CRISPR/Cas9-based genome editing are also presented and summarized.</description><subject>Acids</subject><subject>Bacteria</subject><subject>CRISPR</subject><subject>Dairy products</subject><subject>DNA repair</subject><subject>Editing</subject><subject>Efficiency</subject><subject>Eukaryotes</subject><subject>Food</subject><subject>Genes</subject><subject>Genetic engineering</subject><subject>Genetic modification</subject><subject>Genome editing</subject><subject>Genomes</subject><subject>Gram-positive bacteria</subject><subject>Homologous recombination</subject><subject>Lactic acid</subject><subject>Lactic acid bacteria</subject><subject>Lactobacillus</subject><subject>Mammalian cells</subject><subject>Mutation</subject><subject>Plant cells</subject><subject>Prebiotics</subject><subject>Probiotics</subject><subject>Prokaryotes</subject><subject>Proteins</subject><subject>Review</subject><subject>Strains (organisms)</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkU1LxDAQhoMo7vpx9F7w4qU6Tdo0vQjr-rWw4Pc5pMnsmqVNatMK_nsru4jraQbm4WFeXkJOEjhnrIALu6oDZTRJqMjoDhknKaUxAM93_-wjchDCCmAAs2KfjBhnPOFpPiZP1_iJlW9qdF2knIkmTVNZrTrrXYj8Ipo-z14eny-mKhTxlQpoojt0vsboxtjOumVkXTRXuvOl0raq-nBE9haqCni8mYfk7fbmdXofzx_uZtPJPNasoF1cMjSG5yYFXQgUOeQ0YYDaaCMMQgFIBdCUm5KpRECWAapSLESZ6dQoheyQXK69TV_WaPQQoFWVbFpbq_ZLemXl9sXZd7n0n7LgGYcUBsHZRtD6jx5DJ2sbNFaVcuj7IGnOMsFzADagp__Qle9bN8T7oVLOchBioOI1pVsfQouL32cSkD9lya2y2DfWTIZW</recordid><startdate>20221101</startdate><enddate>20221101</enddate><creator>Mu, Yulin</creator><creator>Zhang, Chengxiao</creator><creator>Li, Taihua</creator><creator>Jin, Feng-Jie</creator><creator>Sung, Yun-Ju</creator><creator>Oh, Hee-Mock</creator><creator>Lee, Hyung-Gwan</creator><creator>Jin, Long</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-3222-8555</orcidid><orcidid>https://orcid.org/0000-0002-2277-5443</orcidid><orcidid>https://orcid.org/0000-0003-0376-0964</orcidid><orcidid>https://orcid.org/0000-0003-3808-5217</orcidid></search><sort><creationdate>20221101</creationdate><title>Development and Applications of CRISPR/Cas9-Based Genome Editing in Lactobacillus</title><author>Mu, Yulin ; 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This review examines the application and current issues of CRISPR/Cas9-based genome editing in Lactobacillus, as well as the development trend of CRISPR/Cas9-based genome editing in Lactobacillus. In addition, the fundamental mechanisms of CRISPR/Cas9-based genome editing are also presented and summarized.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>36361647</pmid><doi>10.3390/ijms232112852</doi><orcidid>https://orcid.org/0000-0003-3222-8555</orcidid><orcidid>https://orcid.org/0000-0002-2277-5443</orcidid><orcidid>https://orcid.org/0000-0003-0376-0964</orcidid><orcidid>https://orcid.org/0000-0003-3808-5217</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acids Bacteria CRISPR Dairy products DNA repair Editing Efficiency Eukaryotes Food Genes Genetic engineering Genetic modification Genome editing Genomes Gram-positive bacteria Homologous recombination Lactic acid Lactic acid bacteria Lactobacillus Mammalian cells Mutation Plant cells Prebiotics Probiotics Prokaryotes Proteins Review Strains (organisms) |
title | Development and Applications of CRISPR/Cas9-Based Genome Editing in Lactobacillus |
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