A CRISPR-Cas9 system for knock-out and knock-in of high molecular weight DNA enables module-swapping of the pikromycin synthase in its native host

Our gene-editing tool has enabled the efficient replacement of extensive and repetitive DNA regions within streptomycetes.

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Publication Details

Journal
Microbial Cell Factories
Published
2025-05-27
DOI
https://doi.org/10.1186/s12934-025-02741-w
Citations
1
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
0.81

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article

A CRISPR-Cas9 system for knock-out and knock-in of high molecular weight DNA enables module-swapping of the pikromycin synthase in its native host

Zhe‐Chong Wang, Adrian T. Keatinge‐Clay, Takeshi Miyazawa, Hayden Stegall
1 citations
Microbial Cell Factories
CRISPR and Genetic Engineering
0.81
article

A CRISPR-Cas9 system for knock-out and knock-in of high molecular weight DNA enables module-swapping of the pikromycin synthase in its native host

Zhe‐Chong Wang, Adrian T. Keatinge‐Clay, Takeshi Miyazawa, Hayden Stegall
article en
1 citations

Abstract

Our gene-editing tool has enabled the efficient replacement of extensive and repetitive DNA regions within streptomycetes.

Microbial Cell FactoriesVol. 24(1)
The University of Texas at Austin (US)
University of Texas at Austin, National Institutes of Health, National Institute of General Medical Sciences
Life in Land
Openalex Percentile: Top 28%
CRISPR and Genetic Engineering
0.81
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