BVD-523 solubility dmso Figure 5 In E. coli, Serratia 39006 PhoB can activate expression from the pigA and rap promoters. β-Galactosidase activity was measured from E. coli cells grown in LB carrying plasmid pTA15 or pTA14 (containing the pigA or rap promoters respectively

cloned upstream of a promoterless lacZ gene) and either an empty vector control (pQE-80L) (solid bar) or pTA74, encoding PhoB (unfilled bar). Pi regulates secondary metabolism and QS in Serratia 39006 In other species, PhoBR upregulates expression of multiple genes when the cell is starved for Pi . As Pi has been shown to control secondary metabolism in multiple species [17], we investigated whether secondary metabolism and QS in Serratia 39006 were also modified by Pi limitation. Growth of Staurosporine mw Serratia 39006 in phosphate-limiting medium (PL medium) without the addition of 5 mM KH2PO4 resulted in an increase in Pig (6-fold) and AHL (2-fold)

production (Fig. 6A &6B), reminiscent of the effects of pstS mutations. β-Galactosidase activity from strains containing chromosomal pigA::lacZ, smaI::lacZ and rap::lacZ fusions grown in PL medium without the addition of 5 mM KH2PO4 was also assessed. Pi limitation resulted in increased transcription of pigA (2-fold) and smaI (5-fold) compared with Pi replete conditions (Fig. 7A &7B), although there was not a clear increase in rap transcription (Fig. 7C). These experiments demonstrate that low Pi, like pstSCAB-phoU mutations, controls the transcription of pigA selleckchem and smaI to up-regulate secondary metabolism and QS.

However, in each instance, the fold increase in response to Pi limitation is lower (by approximately 35%) than that observed in a pst mutant. As the increase in rap transcription in a pst mutant is below 2-fold, a lesser change, cAMP in response to Pi limitation, may be below the level of detection. Figure 6 P i limitation affects secondary metabolism and QS. (A) Pig and (B) AHL production in WT cells were measured throughout growth in phosphate-limiting medium with (squares) or without (triangles) the addition of 5 mM KH2PO4. In all graphs, solid lines represent Pig or AHL assays and dashed lines represent bacterial growth. Figure 7 The effect of P i limitation on pigA, smaI and rap transcription. β-Galactosidase activity was measured from a chromosomal (A) pigA::lacZ (MCP2L), (B) smaI::lacZ (LC13) or (C) rap::lacZ (RAPL) strain throughout growth in phosphate-limiting medium with (squares) or without (triangles) the addition of 5 mM KH2PO4. In all graphs, solid lines represent β-galactosidase assays and dashed lines represent bacterial growth. We predicted that a pstS mutation would be epistatic to the effects of Pi on secondary metabolism and QS. In a pstS mutant, Pi limitation did not result in an increase in maximal Pig production (Fig. 8A), although slightly premature production of Pig was observed (data not shown). In addition, Pi limitation resulted in only a small (1.3-fold) increase in AHL production in a pstS mutant (Fig. 8B).