CRISPR-BEST: a highly efficient DSB-free base editor for filamentous actinomycetes
Yaojun TongiD, Christopher M. WhitfordiD, Helene Lunde RobertseniD, Kai BliniD, Tue Sparholt JørgenseniD, Andreas KlitgaardiD, Tetiana GreniD, Xinglin JiangiD, Tilmann WeberiD, Sang Yup LeeiD
Abstract
Filamentous actinomycetes serve as major producers of various natural products including antimicrobial compounds. Although CRISPR-Cas9 systems have been developed for more robust genetic manipulations, concerns of genome instability caused by the DNA double-strand breaks (DSB) and the toxicity of Cas9 remain. To overcome these limitations, here we report development of the DSB-free, single-nucleotide resolution genome editing system CRISPR-BEST (CRISPR-Base Editing SysTem). Specifically targeted by an sgRNA, the cytidine deaminase component of CRISPR-BEST efficiently converts C:G to T:A within a window of approximately seven-nucleotides. The system was validated and successfully used in different Streptomyces species.
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