| Literature DB >> 30269229 |
Kun-Qiang Hong1,2,3, Ding-Yu Liu1,2,3, Tao Chen1,2,3, Zhi-Wen Wang4,5,6.
Abstract
Genome editing using engineered nucleases has rapidly transformed from a niche technology to a mainstream method used in various host cells. Its widespread adoption has been largely developed by the emergence of the clustered regularly interspaced short palindromic repeats (CRISPR) system, which uses an easily customizable specificity RNA-guided DNA endonuclease, such as Cas9. Recently, CRISPR/Cas9 mediated genome engineering has been widely applied to model organisms, including Bacillus subtilis, enabling facile, rapid high-fidelity modification of endogenous native genes. Here, we reviewed the recent progress in B. subtilis gene editing using CRISPR/Cas9 based tools, and highlighted state-of-the-art strategies for design of CRISPR/Cas9 system. Finally, future perspectives on the use of CRISPR/Cas9 genome engineering for sequence-specific genome editing in B. subtilis are provided.Entities:
Keywords: Bacillus subtilis; CRISPR/Cas9; Genome editing; High-throughout
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Year: 2018 PMID: 30269229 DOI: 10.1007/s11274-018-2537-1
Source DB: PubMed Journal: World J Microbiol Biotechnol ISSN: 0959-3993 Impact factor: 3.312