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. 2017 Mar 9;163(2):280–288. doi: 10.1099/mic.0.000422

Fig. 7.

Fig. 7.

Multicopy expressions of lhrA and hexS inhibit prodigiosin biosynthesis and flhDC expression in the hexS mutant. (a) Prodigiosin pigmentation of strains grown on LB agar with kanamycin for 20 h at 30 °C. Plasmids with the hexS or lhrA genes under control of the Plac promoter inhibit pigmentation in both the wild-type and the ∆hexS mutant. Experiments were performed with the PIC3611 strain background and vector indicates pMQ131. (b) β-Galactosidase activity produced by WT and ∆hexS strains bearing a plasmid-borne flhDC-lacZ transcriptional reporter after growth in LB medium to OD600 3. A representative experiment with three independent biological replicates is shown. Mean and standard deviation is shown. (c) Model, described in Discussion, for coordinated regulation of secondary metabolite biosynthetic genes (pigA-N and swrW) and the prtS protease gene by EepR and HexS. The line between EepR and HexS indicates that each inhibits transcription of the other.