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Highly efficient genome editing in N. gerenzanensis using an inducible CRISPR/Cas9-RecA system.
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- Author(s): Yue X;Yue X; Xia T; Xia T; Wang S; Wang S; Dong H; Dong H; Li Y; Li Y
- Source:
Biotechnology letters [Biotechnol Lett] 2020 Sep; Vol. 42 (9), pp. 1699-1706. Date of Electronic Publication: 2020 Apr 20.- Publication Type:
Journal Article- Language:
English - Source:
- Additional Information
- Source: Publisher: Kluwer Academic Publishers Country of Publication: Netherlands NLM ID: 8008051 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-6776 (Electronic) Linking ISSN: 01415492 NLM ISO Abbreviation: Biotechnol Lett Subsets: MEDLINE
- Publication Information: Publication: 1999- : Dordrecht : Kluwer Academic Publishers
Original Publication: [Kew, Eng., Science and Technology Letters] - Subject Terms:
- Abstract: Objective: To develop an inducible CRISPR/Cas9-Recombinase A (RecA) system to manipulate genes in Nonomuraea gerenzanensis effectively.
Results: Compared with traditional homologous recombination, the inducible CRISPR/Cas9 system achieved 68.8% editing efficiency, whereas, with both the inducible Cas9 and the overexpressed RecA, the efficiency of the combined genome editing system reached 100%. The dbv23-deleted mutant obtained by the inducible CRISPR/Cas9-RecA system was confirmed to produce more A40926 with an approximate yield of 200 mg L -1 than that of around 150 mg L -1 produced by the wild-type strain.
Conclusions: This inducible CRISPR/Cas9-RecA system was successfully constructed and can be utilized as an efficient genome editing tool for Actinomyces able to shorten editing time simultaneously. - Grant Information: ZR2015CL001 Natural Science Foundation of Shandong Province
- Contributed Indexing: Keywords: A40926; CRISPR/Cas9; Genome editing; N. gerenzanensis; RecA
- Accession Number: 0 (Bacterial Proteins)
EC 2.7.7.- (Rec A Recombinases) - Subject Terms: Nonomuraea gerenzanensis
- Publication Date: Date Created: 20200422 Date Completed: 20210224 Latest Revision: 20210224
- Publication Date: 20231215
- Accession Number: 10.1007/s10529-020-02893-2
- Accession Number: 32314149
- Source:
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