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. 2017 Mar 2;4(3):74–89. doi: 10.15698/mic2017.03.561

Figure 3. FIGURE 3: Reversal of the low-PKA phenotype developed in response to iron or zinc deprivation is specific for iron or zinc, respectively.

Figure 3

(A) Growth induction by re-addition of 100 μM of either FeCl3 or ZnCl2 at t = 0 to cells that had been deprived for 4 days in the respective metal ion deprivation media. Growth was measured by determination of OD600. (closed circles) all trace medium, (closed squares) ferrozine iron starvation medium + FeCl3, (open squares) EDTA zinc starvation medium + ZnCl2, (open circles) BPS iron starvation medium + FeCl3, n = 2

(B) Percentage of unbudded cells after re-addition of 100 μM of either FeCl3 or ZnCl2 at t = 0 to cells that had been deprived for 4 days in the respective metal ion deprivation media indicated. The shaded bars represent 0, 2, 4, 8 and 12 h after metal ion re-addition, n = 2.

(C) Trehalose mobilization after re-addition of 100 μM of either FeCl3 or ZnCl2 at t = 0 to cells that had been deprived for 4 days in the respective metal ion deprivation media indicated or had not been starved for iron (CSM-complete).

(D) Glycogen mobilization after re-addition of 100 μM of either FeCl3 or ZnCl2 at t = 0 to cells that had been deprived for 4 days in the respective metal ion deprivation media indicated or had not been starved for iron (CSM-complete).

(C,D) The shaded bars represent 0, 30, 60, 120 and 240 min after metal ion re-addition, n = 2.