4.6 Review

Advances and Perspectives for Genome Editing Tools of Corynebacterium glutamicum

期刊

FRONTIERS IN MICROBIOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2021.654058

关键词

Corynebacterium; molecular genetic modification; CRISPR; Cas system; genome editing; toolbox

资金

  1. National Natural Science Foundation of China [21706133, 21825804, 31670094, 31971343]
  2. Funds for Creative Research Groups of China [31921006]
  3. Key Laboratory of Biomass Chemical Engineering of Ministry of Education, Zhejiang University [2018BCE003]

向作者/读者索取更多资源

Corynebacterium glutamicum is considered a promising biological platform, but faces challenges in genetic manipulation. Recent research shows continuous improvement in genetic manipulation techniques, with CRISPR/Cas-based gene editing tools revolutionizing the field.
Corynebacterium glutamicum has been considered a promising synthetic biological platform for biomanufacturing and bioremediation. However, there are still some challenges in genetic manipulation of C. glutamicum. Recently, more and more genetic parts or elements (replicons, promoters, reporter genes, and selectable markers) have been mined, characterized, and applied. In addition, continuous improvement of classic molecular genetic manipulation techniques, such as allelic exchange via single/double-crossover, nuclease-mediated site-specific recombination, RecT-mediated single-chain recombination, actinophages integrase-mediated integration, and transposition mutation, has accelerated the molecular study of C. glutamicum. More importantly, emerging gene editing tools based on the CRISPR/Cas system is revolutionarily rewriting the pattern of genetic manipulation technology development for C. glutamicum, which made gene reprogramming, such as insertion, deletion, replacement, and point mutation, much more efficient and simpler. This review summarized the recent progress in molecular genetic manipulation technology development of C. glutamicum and discussed the bottlenecks and perspectives for future research of C. glutamicum as a distinctive microbial chassis.

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