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. 2012 Jul 9;6:9. doi: 10.1186/1754-1611-6-9

Figure 2.

Figure 2

CI turning on PRM. (a) A two plasmid system was used to test the ability of PRM activation by CI. This circuit consists of an IPTG inducible plasmid that expresses CI and a reporter plasmid expressing GFP by activation of PRM. Two different ssrA tags were added to the CI protein (ec-ssrA, mf-ssrA) to test the effect of ssrA tags on PRM activation. (b) Fluorescence measurements were normalized to OD600 to account for cell density changes. Strains were cultured in various concentration of IPTG to test for PRM activation. Error bars denote the measurement range (highest and lowest value). All data points were taken with three biological replicates.