Application of Cas12j for IStreptomyces/I Editing

In recent years, CRISPR-Cas toolboxes for Streptomyces editing have rapidly accelerated natural product discovery and engineering. However, Cas efficiencies are oftentimes strain-dependent, and the commonly used Streptococcus pyogenes Cas9 (SpCas9) is notorious for having high levels of off-target t...

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Veröffentlicht in:Biomolecules 2024, Vol.14 (4)
Hauptverfasser: Tan, Lee Ling, Heng, Elena, Leong, Chung Yan, Ng, Veronica, Yang, Lay Kien, Seow, Deborah Chwee San, Koduru, Lokanand, Kanagasundaram, Yoganathan, Ng, Siew Bee, Peh, Guangrong, Lim, Yee Hwee, Wong, Fong Tian
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container_end_page
container_issue 4
container_start_page
container_title Biomolecules
container_volume 14
creator Tan, Lee Ling
Heng, Elena
Leong, Chung Yan
Ng, Veronica
Yang, Lay Kien
Seow, Deborah Chwee San
Koduru, Lokanand
Kanagasundaram, Yoganathan
Ng, Siew Bee
Peh, Guangrong
Lim, Yee Hwee
Wong, Fong Tian
description In recent years, CRISPR-Cas toolboxes for Streptomyces editing have rapidly accelerated natural product discovery and engineering. However, Cas efficiencies are oftentimes strain-dependent, and the commonly used Streptococcus pyogenes Cas9 (SpCas9) is notorious for having high levels of off-target toxicity effects. Thus, a variety of Cas proteins is required for greater flexibility of genetic manipulation within a wider range of Streptomyces strains. This study explored the first use of Acidaminococcus sp. Cas12j, a hypercompact Cas12 subfamily, for genome editing in Streptomyces and its potential in activating silent biosynthetic gene clusters (BGCs) to enhance natural product synthesis. While the editing efficiencies of Cas12j were not as high as previously reported efficiencies of Cas12a and Cas9, Cas12j exhibited higher transformation efficiencies compared to SpCas9. Furthermore, Cas12j demonstrated significantly improved editing efficiencies compared to Cas12a in activating BGCs in Streptomyces sp. A34053, a strain wherein both SpCas9 and Cas12a faced limitations in accessing the genome. Overall, this study expanded the repertoire of Cas proteins for genome editing in actinomycetes and highlighted not only the potential of recently characterized Cas12j in Streptomyces but also the importance of having an extensive genetic toolbox for improving the editing success of these beneficial microbes.
doi_str_mv 10.3390/biom14040486
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subjects Actinomycetes
Control
Genetic aspects
Genetic engineering
Identification and classification
Methods
title Application of Cas12j for IStreptomyces/I Editing
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