Skip to main content
. 2012 Jun;56(6):3392–3394. doi: 10.1128/AAC.00113-12

Fig 2.

Fig 2

In vitro PqnrVC promoter activity in the qnrVC1 gene cassette. Panel A shows an image of E. coli::pGlow-TOPO TA, corresponding to the recircularized vector used as a negative control for background fluorescence. Panels B and C show the green fluorescent protein (GFP)-fluorescent E. coli::pGlow-Pc and E. coli::pGlow-PqnrVC, respectively, resulting from transformation of E. coli TOP10 cells with the pGlow-TOPO TA containing the promoter regions fused into the ATG codon of gfp.