4.7 Article

Pyrabactin, an ABA agonist, induced stomatal closure and changes in signalling components of guard cells in abaxial epidermis of Pisum sativum

Journal

JOURNAL OF EXPERIMENTAL BOTANY
Volume 63, Issue 3, Pages 1349-1356

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jxb/err364

Keywords

Abscisic acid; cytoplasmic pH; fusicoccin; guard cell; nitric oxide; Pisum sativum; pyrabactin; reactive oxygen species; stomatal closure

Categories

Funding

  1. Department of Biotechnology (DBT), New Delhi, India [BT/PR9227/PBD/16/748/2007]
  2. Council of Scientific and Industrial Research (CSIR), New Delhi, India [38(1195)/08/EMR-II]
  3. Department of Science and Technology (DST), New Delhi, India [SR/S2/JCB-06/2006]
  4. CSIR, New Delhi
  5. DST-FIST, New Delhi, India
  6. UGC-SAP-CAS, New Delhi, India
  7. DBT-CREBB, New Delhi, India

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Pyrabactin, a synthetic agonist of abscisic acid (ABA), inhibits seed germination and hypocotyl growth and stimulates gene expression in a very similar way to ABA, implying the possible modulation of stomatal function by pyrabactin as well. The effect of pyrabactin on stomatal closure and secondary messengers was therefore studied in guard cells of Pisum sativum abaxial epidermis. Pyrabactin caused marked stomatal closure in a pattern similar to ABA. In addition, pyrabactin elevated the levels of reactive oxygen species (ROS), nitric oxide (NO), and cytoplasmic pH levels in guard cells, as indicated by the respective fluorophores. However, apyrabactin, an inactive analogue of ABA, did not affect either stomatal closure or the signalling components of guard cells. The effects of pyrabactin-induced changes were reversed by pharmalogical compounds that modulate ROS, NO or cytoplasmic pH levels, quite similar to ABA effects. Fusicoccin, a fungal toxin, could reverse the stomatal closure caused by pyrabactin, as well as that caused by ABA. Experiments on stomatal closure by varying concentrations of ABA, in the presence of fixed concentration of pyrabactin, and vice versa, revealed that the actions of ABA and pyrabactin were additive. Further kinetic analysis of data revealed that the apparent K-D of ABA was increased almost 4-fold in the presence of ABA, suggesting that pyrabactin and ABA were competing with each other either at the same site or close to the active site. It is proposed that pyrabactin could be used to examine the ABA-related signal-transduction components in stomatal guard cells as well as in other plant tissues. It is also suggested that pyrabactin can be used as an antitranspirant or as a priming agent for improving the drought tolerance of crop plants.

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