Fig. 1From: CRISPR/Cas9 mediated editing of the Quorn fungus Fusarium venenatum A3/5 by transient expression of Cas9 and sgRNAs targeting endogenous marker gene PKS12Schematic maps of single guide RNA (sgRNA) expression constructs and the Fusarium venenatum PKS12 gene indicating the target site used for CRISPR/Cas9 editing. A Fv5SrRNA promoter-sgRNA construct, showing positions of PFv5SrRNA, 20 base target site sequence (yellow and black striped box), scaffold sequence (Sc) and terminator (T). B PgdpA dual ribozyme-sgRNA construct showing positions of PgdpA, inverted repeat (blue arrow) of first six bases in target sequence (yellow and black box), HH and HDV ribozyme sequences and trpC terminator (TtrpC). C F. venenatum PKS12 gene showing exons (yellow arrows) and the location of the CRISPR target sequence (pink arrow) in exon 3, 3-14 (‘14’) antisense strand, sequence position 3’–5’ = 238-257Back to article page