Fig. 3From: Construction of a bacteriophage-derived recombinase system in Bacillus licheniformis for gene deletionPartial diagnostic PCR results of the transformants obtained through genome editing using BPR1 are presented (a). Transformants with an edited genetype exhibit a distinct band of 2649 bp, while those with a wild-type genetype display a band of 1947 bp. The recombination effi-ciency was evaluated by cultivating the BLAR strain in media supplemented with rhamnose (BLAR-Rha) or without rhamnose (BLAR), with the wild-type strain BLA serving as a control (b)Back to article page