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Development of a CRISPR/Cas9 genome editing toolbox for Corynebacterium glutamicum

BACKGROUND: Corynebacterium glutamicum is an important industrial workhorse and advanced genetic engineering tools are urgently demanded. Recently, the clustered regularly interspaced short palindromic repeats (CRISPR) and their CRISPR-associated proteins (Cas) have revolutionized the field of genom...

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Autores principales: Liu, Jiao, Wang, Yu, Lu, Yujiao, Zheng, Ping, Sun, Jibin, Ma, Yanhe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693361/
https://www.ncbi.nlm.nih.gov/pubmed/29145843
http://dx.doi.org/10.1186/s12934-017-0815-5
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author Liu, Jiao
Wang, Yu
Lu, Yujiao
Zheng, Ping
Sun, Jibin
Ma, Yanhe
author_facet Liu, Jiao
Wang, Yu
Lu, Yujiao
Zheng, Ping
Sun, Jibin
Ma, Yanhe
author_sort Liu, Jiao
collection PubMed
description BACKGROUND: Corynebacterium glutamicum is an important industrial workhorse and advanced genetic engineering tools are urgently demanded. Recently, the clustered regularly interspaced short palindromic repeats (CRISPR) and their CRISPR-associated proteins (Cas) have revolutionized the field of genome engineering. The CRISPR/Cas9 system that utilizes NGG as protospacer adjacent motif (PAM) and has good targeting specificity can be developed into a powerful tool for efficient and precise genome editing of C. glutamicum. RESULTS: Herein, we developed a versatile CRISPR/Cas9 genome editing toolbox for C. glutamicum. Cas9 and gRNA expression cassettes were reconstituted to combat Cas9 toxicity and facilitate effective termination of gRNA transcription. Co-transformation of Cas9 and gRNA expression plasmids was exploited to overcome high-frequency mutation of cas9, allowing not only highly efficient gene deletion and insertion with plasmid-borne editing templates (efficiencies up to 60.0 and 62.5%, respectively) but also simple and time-saving operation. Furthermore, CRISPR/Cas9-mediated ssDNA recombineering was developed to precisely introduce small modifications and single-nucleotide changes into the genome of C. glutamicum with efficiencies over 80.0%. Notably, double-locus editing was also achieved in C. glutamicum. This toolbox works well in several C. glutamicum strains including the widely-used strains ATCC 13032 and ATCC 13869. CONCLUSIONS: In this study, we developed a CRISPR/Cas9 toolbox that could facilitate markerless gene deletion, gene insertion, precise base editing, and double-locus editing in C. glutamicum. The CRISPR/Cas9 toolbox holds promise for accelerating the engineering of C. glutamicum and advancing its application in the production of biochemicals and biofuels. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-017-0815-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-56933612017-11-24 Development of a CRISPR/Cas9 genome editing toolbox for Corynebacterium glutamicum Liu, Jiao Wang, Yu Lu, Yujiao Zheng, Ping Sun, Jibin Ma, Yanhe Microb Cell Fact Research BACKGROUND: Corynebacterium glutamicum is an important industrial workhorse and advanced genetic engineering tools are urgently demanded. Recently, the clustered regularly interspaced short palindromic repeats (CRISPR) and their CRISPR-associated proteins (Cas) have revolutionized the field of genome engineering. The CRISPR/Cas9 system that utilizes NGG as protospacer adjacent motif (PAM) and has good targeting specificity can be developed into a powerful tool for efficient and precise genome editing of C. glutamicum. RESULTS: Herein, we developed a versatile CRISPR/Cas9 genome editing toolbox for C. glutamicum. Cas9 and gRNA expression cassettes were reconstituted to combat Cas9 toxicity and facilitate effective termination of gRNA transcription. Co-transformation of Cas9 and gRNA expression plasmids was exploited to overcome high-frequency mutation of cas9, allowing not only highly efficient gene deletion and insertion with plasmid-borne editing templates (efficiencies up to 60.0 and 62.5%, respectively) but also simple and time-saving operation. Furthermore, CRISPR/Cas9-mediated ssDNA recombineering was developed to precisely introduce small modifications and single-nucleotide changes into the genome of C. glutamicum with efficiencies over 80.0%. Notably, double-locus editing was also achieved in C. glutamicum. This toolbox works well in several C. glutamicum strains including the widely-used strains ATCC 13032 and ATCC 13869. CONCLUSIONS: In this study, we developed a CRISPR/Cas9 toolbox that could facilitate markerless gene deletion, gene insertion, precise base editing, and double-locus editing in C. glutamicum. The CRISPR/Cas9 toolbox holds promise for accelerating the engineering of C. glutamicum and advancing its application in the production of biochemicals and biofuels. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-017-0815-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-11-16 /pmc/articles/PMC5693361/ /pubmed/29145843 http://dx.doi.org/10.1186/s12934-017-0815-5 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Liu, Jiao
Wang, Yu
Lu, Yujiao
Zheng, Ping
Sun, Jibin
Ma, Yanhe
Development of a CRISPR/Cas9 genome editing toolbox for Corynebacterium glutamicum
title Development of a CRISPR/Cas9 genome editing toolbox for Corynebacterium glutamicum
title_full Development of a CRISPR/Cas9 genome editing toolbox for Corynebacterium glutamicum
title_fullStr Development of a CRISPR/Cas9 genome editing toolbox for Corynebacterium glutamicum
title_full_unstemmed Development of a CRISPR/Cas9 genome editing toolbox for Corynebacterium glutamicum
title_short Development of a CRISPR/Cas9 genome editing toolbox for Corynebacterium glutamicum
title_sort development of a crispr/cas9 genome editing toolbox for corynebacterium glutamicum
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693361/
https://www.ncbi.nlm.nih.gov/pubmed/29145843
http://dx.doi.org/10.1186/s12934-017-0815-5
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