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. Author manuscript; available in PMC: 2021 Nov 3.
Published in final edited form as: Nat Methods. 2020 Oct 19;17(12):1183–1190. doi: 10.1038/s41592-020-00980-w

Figure 1.

Figure 1

A) A schematic of the Type I-C cas gene operon and CRISPR array. The surveillance complex is made up of Cas proteins (Cas51:Cas81:Cas77) and one crRNA, which recruits Cas3 upon target DNA recognition. Cas3 then degrades DNA through its dual helicase-nuclease activity. B) Growth curves of 2 PAO1IC strains expressing different crRNAs targeting phzM (green and orange) compared to a non-targeting strain (blue). Values are the mean of 8 biological replicates each, error bars indicate SD values. C) Cultures resulting from phzM targeting, in the absence of inducer (-ind), presence (+ind), and after recovery. D) Whole-genome sequencing of threePAO1ICself-targeted survivor strains. Bars indicate boundaries of deletions with ORF indicated below; red arrow indicates genomic position of targeted sequences.