Skip to main content
. 2001 Feb 20;98(5):2917–2921. doi: 10.1073/pnas.051616698

Figure 2.

Figure 2

Stomatal performance of wild-type and KAT1∷En-1 plants. (A) Light-induced stomatal opening from wild-type (open bars) and KAT1∷En-1 (filled bars) plants. Stomatal apertures were measured after a 3-h illumination period of epidermal peels incubated in concentrations of KCl as indicated. Mean values (± standard errors) are shown. (B) Stomatal movement in wild-type and KAT1∷En-1 leaves in response to CO2 and ABA. Leaves from predarkened plants were placed in a gas exchange chamber and superfused continuously with CO2-free air for stomatal opening. Application of either 340 ppm of CO2 or 100 μM ABA (arrows) induced stomatal closure, whereas removal of CO2 led to reopening of stomata (arrows). Transpiration rates are given in arbitrary units. Bars represent 20 min and 0.5 mmol m−2 per s, respectively. (C) Apoplastic changes in K+ activity (pK) during light-dependent stomatal opening of representative wild-type and KAT1∷En-1 plants. Following the dark-conditioning characterized by stable K+-activities the application of continuous white light (200 μmol m−2 per s) caused a decrease in the K+ activity (increase in pK) reaching a stable value after ≈20 min.