Abstract

Summary 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‐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.

Highlights

  • Membrane-bound proton-pumping pyrophosphatases utilize inorganic Mg2PPi as an energy-rich compound to drive the uphill transport of protons from the cytosol into the vacuolar lumen

  • Ion pumps are present in relatively high copy numbers compared with ion channels, the turnover numbers of these metabolic energy-fueled machines is only in the order of 10–103 ions sÀ1, so they produce only weak electrical currents (Hedrich, 2012; Lodish et al, 2012)

  • Since in our hands Arabidopsis lines constitutively overexpressing AtAVP1 showed no significant increase in PPi-induced vacuolar currents, we took advantage of N. benthamiana transient transformation (Latz et al, 2007; De Angeli et al, 2013)

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Summary

Introduction

Membrane-bound proton-pumping pyrophosphatases utilize inorganic Mg2PPi as an energy-rich compound to drive the uphill transport of protons from the cytosol into the vacuolar lumen. The type-I H+PPase (designated here as V-PPase) together with the V-ATPases are localized in the vacuolar membrane, while the K+independent type-II H+-PPase resides in the Golgi and leads to the acidification of the Golgi lumen upon proton pumping (Segami et al, 2010). 2 pH units are generated (Krebs et al, 2010; Shen et al, 2013; Wang et al., 2015). These gradients energize the voltage-dependent and proton-driven ion and metabolite transporters (De Angeli et al, 2006; Schulz et al, 2011; Klemens et al, 2014)

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