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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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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. |
format | Online Article Text |
id | pubmed-5693361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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