Fig. 2

The mutagenesis and characterization of pPML. a Comparison of GFP expression driven by promoter P43 and PsrfA. b SDS-PAGE analysis of GFP expression driven by P43 and PsrfA. c Verification of the fluorescence intensity of the four representative mutants at the 24-h cultivation in the scale of the shake flask. The experiments were repeated independently in triplicate. The data were shown by mean ± S.D. d SDS-PAGE analysis of the GFP expression levels in the four selected mutants. The whole-cell proteins of each sample were separated by 12% SDS-PAGE and were then stained with Coomassie Brilliant Blue R-250. CK denoted the strain without any plasmid