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. 2008 Oct 22;105(43):16602–16607. doi: 10.1073/pnas.0808807105

Fig. 2.

Fig. 2.

The ClpX-mediated degradation of CpdR is dependent on its phosphorylation state and on DivK. (A) WT cells harboring the plasmid pPxylX-clpX* (14) were grown in M2G medium in the absence of xylose. Culture samples were incubated for 4 h either in the absence (solid line) or in the presence of xylose to allow clpX* induction (dashed line). (B) Pulse–chase experiments showing the half-lives of CpdR (black lines) and CpdRD51A (gray lines) in the presence (solid lines) or absence (dashed lines) of DivK. Each strain was incubated in the presence of xylose to induce cpdR or cpdRD51A and in the presence or absence of vanillate (presence or absence of DivK, respectively). R2 is the regression coefficient.