Fig. 3
From: A RecET-assisted CRISPR–Cas9 genome editing in Corynebacterium glutamicum
Applicability of CRISPR–Cas9 editing method in C. pekinense. a The transformation efficiency of pHAsgRNA argR and pHAsgRNA farR to C. glutamicum ATCC 13032 and C. pekinense 1.563 for knockout of argR and farR genes. b Colony PCR identification for argR deletion in C. glutamicum ATCC 13032 and C. pekinense 1.563. c Colony PCR identification for farR deletion in C. glutamicum ATCC 13032 and C. pekinense 1.563