Journal of Experimental Botany, Vol. 51, No. 343, pp. 147-158,
February 2000
© 2000 Oxford University Press
pH, abscisic acid and the integration of metabolism in plants under stressed and non-stressed conditions: cellular responses to stress and their implication for plant water relations
School of Biochemistry and Molecular Genetics, University of New South Wales, Sydney, 2052, Australia
A paradigm for the response of plants to stress is presented which suggests that plants move towards a state of minimal metabolic activity as a stress intensifies and remain in that state until that stress is relieved. The paradigm is based on the proposition that cells that interface with the transpiration stream employ variations on the following theme to move towards that state. Tension on the apoplastic water opens a mechanosensitive Ca2+ channel, a response that is augmented by apoplastic ABA. The resulting elevated cytoplasmic Ca2+ deactivates a plasmalemma H+/ATPase and also activates a K+-H+ symport. The inflow of K+ and H+ depolarizes the membrane and renders the apoplast less acidic, the protons being removed to the vacuole and the K+ ions being re-exported via the K+ outward rectifying channel. The onset of darkness in guard and mesophyll cells deactivates the plasmalemma H+/ATPase and then the events outlined above ensue except that these cells do not appear to utilize either Ca2+ or ABA during these changes. In stressed cells it is proposed that elevated cytoplasmic Ca2+ activates the release of an ABA precursor from a stored form. ABA is then released in the apoplast after export of the precursor if the activity of the K+ -H+ symport has brought the apoplastic pH close to 7.0. It is proposed that aquaporins in the xylem parenchyma and mesophyll cells are opened by elevated cytoplasmic Ca2+ when the water potential of the transpiration stream is high so that water can be stored in the xylem parenchyma reservoir. The water in this reservoir is then used to increase the water potential in the transpiration stream when the water column is under tension and to help repair embolisms by a mechanism that resembles stomatal closure.
Key words: Apoplastic pH, ABA, stress, plant water relations, H+/ATPase.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
A. G. Netting Limitations within "The Limits to Tree Height"1 Am. J. Botany, February 1, 2009; 96(2): 542 - 544. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. W. Koch and S. C. Sillett A response to: Limitations within "The Limits to Tree Height" Am. J. Botany, February 1, 2009; 96(2): 545 - 547. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Aroca, P. Vernieri, and J. M. Ruiz-Lozano Mycorrhizal and non-mycorrhizal Lactuca sativa plants exhibit contrasting responses to exogenous ABA during drought stress and recovery J. Exp. Bot., May 9, 2008; (2008) ern057v1. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. P. Lee, C. Kim, F. Landgraf, and K. Apel EXECUTER1- and EXECUTER2-dependent transfer of stress-related signals from the plastid to the nucleus of Arabidopsis thaliana PNAS, June 12, 2007; 104(24): 10270 - 10275. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. A. Else, J. M. Taylor, and C. J. Atkinson Anti-transpirant activity in xylem sap from flooded tomato (Lycopersicon esculentum Mill.) plants is not due to pH-mediated redistributions of root- or shoot-sourced ABA J. Exp. Bot., September 1, 2006; 57(12): 3349 - 3357. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. G. L. op den Camp, D. Przybyla, C. Ochsenbein, C. Laloi, C. Kim, A. Danon, D. Wagner, E. Hideg, C. Gobel, I. Feussner, et al. Rapid Induction of Distinct Stress Responses after the Release of Singlet Oxygen in Arabidopsis PLANT CELL, October 1, 2003; 15(10): 2320 - 2332. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. C. Dodd, L. P. Tan, and J. He Do increases in xylem sap pH and/or ABA concentration mediate stomatal closure following nitrate deprivation? J. Exp. Bot., April 1, 2003; 54(385): 1281 - 1288. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. TUBEROSA, S. SALVI, M. C. SANGUINETI, P. LANDI, M. MACCAFERRI, and S. CONTI Mapping QTLs Regulating Morpho-physiological Traits and Yield: Case Studies, Shortcomings and Perspectives in Drought-stressed Maize Ann. Bot., June 15, 2002; 89(7): 941 - 963. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. M. Holbrook, V.R. Shashidhar, R. A. James, and R. Munns Stomatal control in tomato with ABA-deficient roots: response of grafted plants to soil drying J. Exp. Bot., June 1, 2002; 53(373): 1503 - 1514. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Bahrun, C. R. Jensen, F. Asch, and V. O. Mogensen Drought-induced changes in xylem pH, ionic composition, and ABA concentration act as early signals in field-grown maize (Zea mays L.) J. Exp. Bot., February 1, 2002; 53(367): 251 - 263. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. Van Ieperen, J. Nijsse, C.J. Keijzer, and U. Van Meeteren Induction of air embolism in xylem conduits of pre-defined diameter J. Exp. Bot., May 1, 2001; 52(358): 981 - 991. [Abstract] [Full Text] [PDF] |
||||
![]() |
C.L. V. Santos, A. Campos, H. Azevedo, and G. Caldeira In situ and in vitro senescence induced by KCl stress: nutritional imbalance, lipid peroxidation and antioxidant metabolism J. Exp. Bot., February 1, 2001; 52(355): 351 - 360. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. J. Davies, M. A. Bacon, D. Stuart Thompson, W. Sobeih, and L. Gonzalez Rodriguez Regulation of leaf and fruit growth in plants growing in drying soil: exploitation of the plants' chemical signalling system and hydraulic architecture to increase the efficiency of water use in agriculture J. Exp. Bot., September 1, 2000; 51(350): 1617 - 1626. [Abstract] [Full Text] [PDF] |
||||




