A reassessment of the intervention of calmodulin in the regulation of stomatal movement

Abstract

Commelina cammunis L., a monocotyledonous plant whose stomata are highly sensitive to calcium ions, was used to study calmodulin (CaM) involvement in stomatal movements. CaM was detected and quantified in guard cell and mesophyll cell protoplasts by western blot and by 45Ca2+‐overlays. CaM was found to be 3‐ to 7‐fold more abundant on a per protein basis in guard cell than in mesophyll cell protoplasts. Numerous guard cell proteins that bind CaM in a Ca2+‐dependent manner were detected by gold‐labelled CaM overlays. Using bioassays with epidermal strips, different CaM‐antagonists were found to induce a net stimulation of stomatal opening in darkness or under illumination (trifluoperazine > compound 48/80 ≅ fluphenazine > W7 > W5). As CaM is frequently involved in the regulation of phosphorylation processes, the effects of different inhibitors of protein kinases on stomatal movements were studied. In red plus blue light, a promotion of the stomatal aperture was observed in the nanomolar range with K252a and KT5926 and in the micromolar range with KT5720 ≫ ML7 ≅ ML9 ≫ H7 > KN62. Only the inhibitors with a high specificity for Ca2+‐CaM dependent protein kinases (K252a, KT5926, ML7, ML9) triggered a stomatal opening in darkness and increased stomatal aperture in red plus blue light. Taken together, these data strongly suggest that a Ca2+‐ or a Ca2+‐CaM‐dependent protein kinase plays a central role in the calcium transduction pathway leading to the maintaining of stomatal closure.