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High V-PPase activity is beneficial under high salt loads, but detrimental without salinity

Please always quote using this URN: urn:nbn:de:bvb:20-opus-227553
  • The membrane-bound proton-pumping pyrophosphatase (V-PPase), together with the V-type H+-ATPase, generates the proton motive force that drives vacuolar membrane solute transport. Transgenic plants constitutively overexpressing V-PPases were shown to have improved salinity tolerance, but the relative impact of increasing PPi hydrolysis and proton-pumping functions has yet to be dissected. For a better understanding of the molecular processes underlying V-PPase-dependent salt tolerance, we transiently overexpressed the pyrophosphate-drivenThe membrane-bound proton-pumping pyrophosphatase (V-PPase), together with the V-type H+-ATPase, generates the proton motive force that drives vacuolar membrane solute transport. Transgenic plants constitutively overexpressing V-PPases were shown to have improved salinity tolerance, but the relative impact of increasing PPi hydrolysis and proton-pumping functions has yet to be dissected. For a better understanding of the molecular processes underlying V-PPase-dependent salt tolerance, we transiently overexpressed the pyrophosphate-driven proton pump (NbVHP) in Nicotiana benthamiana leaves and studied its functional properties in relation to salt treatment by primarily using patch-clamp, impalement electrodes and pH imaging. NbVHP overexpression led to higher vacuolar proton currents and vacuolar acidification. After 3 d in salt-untreated conditions, V-PPase-overexpressing leaves showed a drop in photosynthetic capacity, plasma membrane depolarization and eventual leaf necrosis. Salt, however, rescued NbVHP-hyperactive cells from cell death. Furthermore, a salt-induced rise in V-PPase but not of V-ATPase pump currents was detected in nontransformed plants. The results indicate that under normal growth conditions, plants need to regulate the V-PPase pump activity to avoid hyperactivity and its negative feedback on cell viability. Nonetheless, V-PPase proton pump function becomes increasingly important under salt stress for generating the pH gradient necessary for vacuolar proton-coupled Na+ sequestration.show moreshow less

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Metadaten
Author: Dorothea Graus, Kai R. Konrad, Felix Bemm, Meliha Görkem Patir Nebioglu, Christian Lorey, Kerstin Duscha, Tilman Güthoff, Johannes Herrmann, Ali Ferjani, Tracey Ann Cuin, M. Rob G. Roelfsema, Karin Schumacher, H. Ekkehard Neuhaus, Irene Marten, Rainer Hedrich
URN:urn:nbn:de:bvb:20-opus-227553
Document Type:Journal article
Faculties:Fakultät für Biologie / Julius-von-Sachs-Institut für Biowissenschaften
Fakultät für Biologie / Center for Computational and Theoretical Biology
Language:English
Parent Title (English):New Phytologist
Year of Completion:2018
Volume:219
Pagenumber:1421-1432
Source:New Phytologist (2018) 219:1421-1432. https://doi.org/10.1111/nph.15280
DOI:https://doi.org/10.1111/nph.15280
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Tag:cell death; plasma membrane voltage; proton pump currents; salt; vacuolar pH; vacuolar proton-ATPase (V-ATPase); vacuolar proton-pyrophosphatase (V-PPase)
Release Date:2024/09/05
Licence (German):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International