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Plant Physiol. Author manuscript; available in PMC 2011 January 10.
Published in final edited form as:
PMCID: PMC2996032
EMSID: UKMS33623

Osmoregulation in Lilium Pollen Grains Occurs via Modulation of the Plasma Membrane H+ ATPase Activity by 14-3-3 Proteins1,[C][W][OA]

Abstract

To allow successful germination and growth of a pollen tube, mature and dehydrated pollen grains (PGs) take up water and have to adjust their turgor pressure according to the water potential of the surrounding stigma surface. The turgor pressure of PGs of lily (Lilium longiflorum) was measured with a modified pressure probe for simultaneous recordings of turgor pressure and membrane potential to investigate the relation between water and electrogenic ion transport in osmoregulation. Upon hyperosmolar shock, the turgor pressure decreased, and the plasma membrane (PM) hyperpolarizes in parallel, whereas depolarization of the PM was observed with hypoosmolar treatment. An acidification and alkalinization of the external medium was monitored after hyper- and hypoosmotic treatments, respectively, and pH changes were blocked by vanadate, indicating a putative role of the PM H+ ATPase. Indeed, an increase in PM-associated 14-3-3 proteins and an increase in PM H+ ATPase activity were detected in PGs challenged by hyperosmolar medium. We therefore suggest that in PGs the PM H+ ATPase via modulation of its activity by 14-3-3 proteins is involved in the regulation of turgor pressure.

Plant cells, surrounded by a rigid cell wall, have an internal hydrostatic pressure, the turgor pressure. The turgor pressure depends on the concentration gradient of osmolytes across the plasma membrane (PM); therefore, changes in osmolytes lead to turgor-driven movements of entire plant organs, e.g. leaves of Samanea saman (Moran, 2007), Dionea trap leaves (Hodick and Sievers, 1989), or changes in the cell shape of guard cells (Roelfsema and Hedrich, 2005). Especially in guard cells turgor pressure values can reach up to 0.12 MPa (12 bar; Franks et al., 1998). Turgor pressure values can be estimated indirectly by observing plasmolysis or directly measured by impaling a pressure probe into the living plant cell still surrounded by an intact cell wall (Hüsken et al., 1978). The use of a pressure probe not only allows the monitoring of the turgor pressure over a time period but also determination of the hydraulic conductivity of the PM (LP), the elastic modulus of the cell wall (ε), and measurements of the permeability of substances across the PM (σ; Zimmermann, 1989; Steudle, 1993; Boyer, 1995; Tomos and Leigh, 1999). In guard cells changes in the activity of a number of ion transporters in the PM lead to a change in the concentration gradient of osmolytes and therefore, water following its potential gradient will either increase or decrease the turgor pressure, thus leading to opening and closing of the stomata, respectively (Roelfsema and Hedrich, 2005; Pandey et al., 2007). On the other hand, environmental changes, e.g. in the water potential of the soil will affect the turgor pressure of root cells that are responding to maintain their turgor pressure (Frensch and Hsiao, 1994). In hyperosmotically stressed Arabidopsis (Arabidopsis thaliana) root cells, a rapid, transient hyperpolarization of the PM was observed, whereas during recovery of turgor pressure, an uptake of ions (K+,Cl,Na+) was measured (Shabala and Lew, 2002). Furthermore, in suspension culture cells, hyper- and hypoosmotic shock caused corresponding changes in turgor pressure and also induced an acidification and alkalinization of the external medium, respectively, mainly carried by modulation of the PM H+ ATPase activity via 14-3-3 protein binding (Reuveni et al., 1987; Curti et al., 1993; Babakov et al., 2000; Felix et al., 2000; Kerkeb et al., 2002). This correlation between changes in turgor pressure and ion transport processes is widespread and can be observed in different plant organs and also in algae and fungi (Lew, 1996; Shabala et al., 2000; Lew et al., 2004; Bisson and Beilby, 2008). Therefore, one may assume that ion and water transport in plant cells are connected to each other not only by affecting physical parameters important for both transport processes (e.g. osmolyte/ion concentration and pressure) but also because of active regulation and signal cross talk between both processes as has been shown in yeast (Saccharomyces cerevisiae) cells (Muzzey et al., 2009).

Pollen grains (PGs), the male gametophytes of higher plants, are exposed to dramatic changes in environmental water potential. In the last stage of maturation, PGs are dehydrated and are then transferred to a stigma surface on which they will immediately take up water to rehydrate. Before germination occurs, the internal ion concentrations, pH, and also the turgor pressure have to be adjusted to allow the germination and growth of a pollen tube (PT) through the pistil tissue toward the ovules (Feijó et al., 1995). PGs do not foresee the water potential of the stigma on which they are going to land; interestingly, in vitro-cultivated PGs of the same species are capable of germinating in media containing various concentrations of osmolytes, e.g. lily (Lilium longiflorum) PGs can germinate in 5% to 12% Suc corresponding to 150 and 450 mosmol kg−1, respectively, with a more or less constant turgor pressure independent from the medium osmolality (Benkert et al., 1997). On the other hand, growing PTs are very sensitive to osmotic changes in the medium and stopped growth or increased the volume of the tip region (tip swelling; Pierson et al., 1994; Zonia and Munnik, 2004). The turgor pressure of lily PTs stays more or less constant (0.21 ± 0.06 MPa) and is independent from tube growth rates, tube length, and medium osmolality (Benkert et al., 1997). Artificial increases of turgor pressure by the pressure probe immediately stopped growth and further increase resulted in bursting of the tube tip with a burst pressure approximately twice the previous pressure, indicating a fine-regulated balance between turgor pressure and cell wall strength at the tube tip that is necessary for successful growth of PTs (Winship et al., 2010). However, PTs and grains are surrounded by an electrical field that is generated by localized influxes and effluxes of ions (Holdaway-Clarke and Hepler, 2003; Michard et al., 2009), thus changing the cytosolic osmolyte concentration. Additionally, metabolic activity during PT growth will also contribute to variations in osmolyte concentrations that will result in changes in the cytosolic water potential and, therefore, in water flux amount across the PM or even water flux direction. Therefore, one may assume an osmoregulation mechanism taking place in PGs that (1) somehow senses the osmotic conditions on the stigma surface, (2) allows an influx of water to account for the volume increase in germination and tube growth, and (3) adapts the turgor pressure to grow a PT without bursting. Several cellular components that are involved in osmoregulation as demonstrated for other plant cells were detected in pollen, too: ion channels (Obermeyer and Blatt, 1995; Fan et al., 1999; Mouline et al., 2002; Griessner and Obermeyer, 2003; Frietsch et al., 2007; Sze et al., 2004), a PM H+ ATPase (Obermeyer et al., 1996; Certal et al., 2008; Pertl et al., 2009), and 14-3-3 proteins (Pertl et al., 2005). In this study, invasive and noninvasive techniques were used to investigate whether PGs are capable to adjust and regulate their turgor pressure and which transport activities are affected by turgor changes and, therefore, are involved in osmoregulation of PGs.

RESULTS

PG Turgor Pressure and Membrane Potential

Immediately after impalement with the micropipette of the pressure probe, a stable turgor pressure of 0.317 ± 0.07 MPa (n = 17) was recorded in lily PGs bathed in standard medium (298 mM mannitol; Fig. 1). Exposing the PGs to various external mannitol concentrations that still allow germination and tube growth (Benkert et al., 1997), resulted in an adaptation of the turgor pressure to the new osmotic condition. The turgor pressure decreased to a lower value when the measuring chamber was perfused with a medium of higher osmolality (398 mM mannitol) or increased upon perfusion with a lower osmolar medium (198 mM mannitol; Fig. 1A). The changes in turgor pressure were always reversible in the range of media used for perfusion (approximately 50–520 mosmol kg−1) and lily PGs behave like a linear osmometer (Fig. 1B), indicating a reflection coefficient close to 1 for mannitol. At least no changes in the concentration of mannitol during the experiment due to an uptake by the PGs were detectable. A similar linear osmotic behavior was observed when lily PG protoplasts were exposed to various mannitol concentrations (Sommer et al., 2007). The osmotic potential of the cytosol could be estimated as 580 mosmol kg−1 from the regression line (Fig. 1B). During some measurements, the turgor pressure was manually changed by the pressure probe and its relaxation was recorded (Supplemental Fig. S1) to determine the hydraulic conductivity of the PM. The LP was calculated from the half time of the turgor pressure relaxations according to Steudle (1989) and Zimmermann (1989), giving 4.89 ± 5.20 10−8 m MPa−1s−1 (n = 14) that corresponds to an osmotic permeability coefficient (Pos) of approximately 7.4 μm s−1 that is well in the range of Pos values determined by swell assays of lily PG protoplasts (6.6 μm s−1; Sommer et al., 2007).

Figure 1
Turgor pressure of PGs. A, A lily PG was impaled with the pressure probe in standard medium (298 mM mannitol). Perfusion of the chamber with hyper- (398 mM mannitol) and hypoosmolar (198 mM mannitol) media resulted in a reversible change of turgor pressure. ...

To monitor effects on electrogenic transport processes across the PM in parallel to turgor pressure changes, simultaneous measurements of the turgor pressure and the membrane potential were performed by impaling the PG with a micropipette that was partially filled with an electrolyte (1 M KCl) to ensure contact with an Ag/AgCl wire connected to a voltage amplifier (Fig. 2A). A glass capillary inside the micropipette allowed an electrical contact between the cytosol and the electrolyte-filled part of the pressure probe thus measuring the membrane potential of the impaled PG (Zhu, 1996). The PG turgor pressure values measured by the modified pressure probe were similar to those recorded with the original pressure probe. Perfusion with a hypoosmotic medium (198 mM mannitol) increased the turgor pressure and simultaneously depolarized the PM (Fig. 2B), whereas upon perfusion with a hyperosmotic medium (398 mM mannitol) the turgor pressure decreased as expected and the PM was hypolarized (Fig. 2C). For each measured PG, the change in medium osmolality (Δosmol) was plotted against the corresponding change in membrane potential (ΔVM), giving a linear relation with hyperosmotic media causing hyperpolarization and hypoosmotic media resulted in depolarization of the PM (Fig. 2D). These deflections of the membrane potential indicate the presence of an electrogenic transport process that is coupled to or responds to turgor pressure changes in lily PGs.

Figure 2
Simultaneous measurement of turgor pressure and membrane potential in single PGs. A, Modified pressure probe with a chlorided silver wire reaching into the electrolyte solution. Except for the indicated part of the micropipette, the pressure probe as ...

External pH Changes upon Osmotic Stress

PGs incubated in in vitro germination medium extrude H+ and acidify the external medium (Southworth, 1983; Rodriguez-Rosales et al., 1989). The acidification of the external medium is inhibited by vanadate and promoted by fusicoccin, two well-characterized modulators of the PM H+ ATPase in plants. Therefore, monitoring a vanadate-sensitive acidification of the external medium provides a noninvasive method to record the PM H+ ATPase activity during various osmotic treatments. Under standard osmotic conditions (298 mM mannitol) an acidification of the medium was recorded for 1 h after suspending the lily PGs in the incubation chamber (Supplemental Fig. S2). Addition of 500 μM Na+ vanadate clearly inhibited acidification (Fig. 3B; Supplemental Fig. S2), whereas the addition of 1 μM fusiccocin stimulated the H+ extrusion (Supplemental Fig. S2). Immediately after the exposure to hypo- or hyperosmotic solutions, transient changes in the acidification rate could be observed, leading to a slight alkalinization or to a faster acidification during the first 100 s after osmotic stress (Fig. 3A). Addition of an isoosmotic solution did not affect the previously recorded acidification rate (Fig. 3A). The observed alkalinization as well as the acidification after the osmotic stress were both sensitive to vanadate. In the presence of 500 μM Na+ vanadate, almost no changes in the external pH were detectable after osmotic shock (Fig. 3B). Thus, the activity of the PM H+ ATPase might be responsible for the pH as well as for the membrane potential changes induced by osmotic challenges. Therefore, one might assume that during exposure to hyperosmotic conditions, the PM H+ ATPase activity is increased, resulting in a hyperpolarization of the PM and a higher acidification rate of the external medium; on the contrary, a hypoosmotic stress reduces the PM H+ ATPase activity, leading to a depolarization of the PM and a transient alkalinization of the medium.

Figure 3
Vanadate-sensitive H+ transport changes upon hypo- and hyperosmotic shock. A, PGs were incubated in standard medium (298 mM mannitol), and the pH of the external medium was monitored. Upon sudden osmotic changes (198, 298, and 398 mM mannitol) at t = ...

PM-Associated 14-3-3s and PM H+ ATPase Activity

To test whether the up- or down-regulation of the PM H+ ATPase activity is mediated by 14-3-3 proteins, the abundance of PM-associated 14-3-3 proteins after different osmotic treatments was detected. Intact PGs were suspended in standard germination medium M (298 mM mannitol) for 15 min and were then incubated in iso-, hypo-, and hyperosmolar medium M for another 15 min before PM vesicles were isolated by Suc step gradient centrifugation. The amount of PM H+ ATPases was unaffected by the osmotic treatment, showing similar band intensities after immunodetection in the crude membrane (membrane fraction [MF]) as well as in the PM-enriched fraction (PMF; Fig. 4, A and B, left). The amount of 14-3-3 proteins in the soluble protein, cytosolic fraction (CF), was also not affected upon osmotic treatment, whereas membrane-associated 14-3-3 proteins clearly show a decrease, no effect, and an increase in the crude MF after hypo-, iso-, and hyperosmolar treatments, respectively (Fig. 4A). In isolated PM vesicles, 14-3-3 proteins were detected with two different antibodies (MUP5 and MUP15; Pertl et al., 2005) and showed changes in signal intensities upon osmotic treatments (Fig. 4B). Compared with controls (isoosmolar treatment) hypo- and hyper-osmotic shock resulted in less or more PM-associated 14-3-3 proteins (Fig. 4B) that was confirmed in three independent PMF preparations after osmotic shock treatment. The Coomassie-stained protein gel (Fig. 4C) serves as a loading control to demonstrate the equal amounts of protein loaded on each lane. In addition, similar results were observed when 14-3-3 proteins in the PMF were detected with antibodies against Arabidopsis 14-3-3s (at-82, Santa Cruz Biotechnology) and Hordeum vulgare 14-3-3s (Hv14-3-3A, Hv14-3-3B, Hv14-3-3C, Agrisera; and gifts from Bert de Boer; data not shown).

Figure 4
PM H+ ATPase and membrane-associated 14-3-3 proteins after osmotic treatment. PGs were incubated in standard medium (298 mM mannitol) for 15 min and exposed to different media osmolalities (198, 298, 398 mM mannitol) for another 15 min. The cytosolic ...

Additionally, an increase in vanadate-sensitive ATP hydrolysis was detectable after hyperosmolar treatment, indicating an activation of the PM H+ ATPase activity in PM-enriched vesicles (Table I). Compared with the ATPase activity under isoosmotic conditions the vanadate-sensitive ATPase activity decreased by 30% after hypoosmotic shock whereas upon hyperosmotic treatment the ATPase activity increased by 26%, probably due to the interaction with 14-3-3 proteins.

Table I
PM H+ ATPase activity

DISCUSSION

Generally, PTs growing in in vitro culture are very sensitive to external perturbations and stop growth immediately or even burst at their tips. Small changes in external parameters like pH, K+, and Ca2+ concentrations or osmolality lead to temporal cessation of growth or change in growth rate oscillations that are often accompanied by morphological changes of the tube tip region (Pierson et al., 1994; Malhó and Trewavas, 1996; Messerli and Robinson, 2003; Zonia and Munnik, 2004; Zerzour et al., 2009). This flexibility to react to small environmental changes may help the PT to grow toward the ovary as fast as possible despite varying conditions along the style. In particular, PTs have to adapt their cell wall strength to osmotic changes that would otherwise lead to tube bursting (Zerzour et al., 2009; Winship et al., 2010). The mechanisms and pathways, how PTs sense or regulate their turgor pressure, osmolyte concentrations, and water fluxes, are still not well characterized. PGs also need to adapt to osmotic conditions of their environment, especially after landing on a receptive stigma when they first take up water and have to adjust their internal ion and osmolyte concentrations to build up a turgor pressure that drives the germination of the tube but still is balanced with the cell wall strength to prevent bursting of the germinating grain (Winship et al., 2010). In contrast to growing PTs that reflect osmotic changes irreversibly in their tube morphology, most manipulations, osmotic changes in particular (Fig. 1), are reversible in PGs, making them a suitable experimental system for first investigations of the principles of osmoregulation in pollen.

The turgor pressure immediately responded to osmotic changes, and lily PGs react like a linear osmometer using mannitol as an osmolyte (Fig. 1). Simultaneously with the turgor pressure the membrane potential difference (VM) also changed, resulting in a hyper- and depolarization of the PM after hyper- and hypoosmotic shock, respectively (Fig. 2D). Similar changes in VM upon osmotic treatments have been reported from other plant cells: In broad bean (Vicia faba) mesocarp cells VM was sensitive to tugor pressure changes (Li and Delrot, 1987) and Arabidopsis root cells showed a transient hyperpolarization after addition of 100 mM mannitol (Shabala and Lew, 2002). A correlation between turgor pressure and changes in VM or in electrogenic transport across the PM was also reported from algal and fungal cells (Bisson and Kirst, 1995; Lew et al., 2004; Lew and Levina, 2007; Bisson and Beilby, 2008). In Arabidopsis and carrot (Daucus carota) cell culture cells (Reuveni et al., 1987; Curti et al., 1993) as well as in leaf mesophyll tissue of beans (Phaseolus vulgaris; Shabala et al., 2000), an increase in (vanadate-sensitive) proton extrusion was detected after turgor pressure decreases by external addition of mannitol, indicating an involvement of the PM H+ ATPase in the turgor pressure-induced changes in VM. By measuring the pH changes (acidification or alkalinization) of the germination medium during in vitro culturing of pollen, the activity of the PM H+ ATPase can be recorded in a noninvasive way (Southworth, 1983; Tupy and Rihova, 1984; Rodriguez-Rosales et al., 1989). In lily pollen cultures a vanadate-sensitive and fusicoccin-stimulated acidification is detectable (Supplemental Fig. S2) and upon hyper- and hypoosmotic treatment an acidification and alkalinization, respectively, was observed (Fig. 3). Both changes in external pH could be inhibited by vanadate, indicating that the changes in VM are caused by changes in the electrogenic H+ transport of the PM H+ ATPase that are also reflected in the increase or decrease of the ATP hydrolysis activity of the PM H+ ATPase. In general, the activity of PM H+ ATPase is modulated by the binding of 14-3-3 proteins to the C-terminal autoinhibitory domain that has been reversibly phosphorylated (see Duby and Boutry, 2009 and refs. therein). 14-3-3 proteins have been detected in almost all cellular compartments of lily PGs and tubes (Pertl et al., 2005) and an increase in PM-associated 14-3-3 proteins is observed after treatment of PGs with hyperosmotic medium. A similar correlation between hyperosmolar treatment, activated H+ transport, or H+ efflux and abundance of 14-3-3 proteins at the PM was observed in suspension-cultured cells of tomato (Solanum lycopersicum; Kerkeb et al., 2002) and sugar beet (Beta vulgaris; Babakov et al., 2000). In contrast to Kerkeb et al. (2002) who observed an increase only in H+ transport but not in ATP hydrolysis activity upon hyperosmotic shock with NaCl, the H+ transport and the ATP hydrolysis of the PM ATPase in lily PGs are both stimulated by hyperosmotic treatment with mannitol.

CONCLUSION

These data support the hypothesis that short-term osmoregulation in plants cells including PGs, involves a modulation of the PM H+ ATPase activity by interactions with 14-3-3 proteins (Fig. 5). Upon hyperosmolar shock, the turgor pressure decreases and a hyperpolarization of the PM can be measured due to an activation of the PM H+ ATPase via 14-3-3 interaction. Consequently, a membrane potential more negative than the reversal potential of K+ allows a higher K+ influx that in turn promotes water uptake to readjust the turgor pressure in the long term. On the other hand, a hypoosmotic shock increases the turgor pressure and down-regulates the PM H+ ATPase activity via dissociation of 14-3-3 proteins. The resulting depolarization of the PM enables K+ efflux followed by water efflux and the turgor pressure finally decreases again to the previous value. The short-term effects on turgor pressure and H+ ATPase activity have been measured in this study whereas the hypothesized changes in K+ and water transport and the subsequent readjustment of the turgor pressure still need to be demonstrated. Additionally, due to the fact that the interaction between the C-terminal autoinhibitory domain of the PM H+ ATPase and 14-3-3 proteins requires a change in the phophorylation status of probably both proteins several kinase- and phosphatase-including signal transduction pathways may be involved, e.g. a MAP kinase kinase is activated upon hydration of tobacco (Nicotiana tabacum) pollen (Voronin et al., 2004). Although the knowledge on osmoregulation in plant cells is still fragmentary, PGs may serve as a suitable model system for investigating plant osmoregulation and search for an osmosensor.

Figure 5
Schematic summary of osmoregulation in lily PGs. The first two events after osmotic shock were measured in this study. Subsequent, hypothetical events finally leading to a readjustment of turgor pressure are given in italics. For further explanation see ...

MATERIALS AND METHODS

Plant Material

Lily (Lilium longiflorum) plants were grown in a greenhouse under environmental light and temperature conditions. PGs were collected from fully developed flowers and either used immediately or frozen as single anthers (turgor pressure measurements and pH measurements) or in aliquots of 25 flowers (biochemical experiments) in liquid N2 and stored at −80°C. In parallel to or before the experiments, aliquots of the frozen PG batches were tested for their germination ability. In all experiments shown, no differences in germination frequency or tube morphology were observed between the frozen and fresh pollen.

Combined Turgor Pressure and Membrane Potential Measurements

The turgor pressure of ungerminated PGs was measured with the pressure probe (Zimmermann et al., 1969) as described in Benkert et al. (1997). Ungerminated PGs were suspended in standard bath medium [Med M, in mM: 298 mannitol, 1 KCl, 0.1 Ca(OH)2, 1.6 H3BO3, 25 MES adjusted to pH 5.6 with Tris (Tris{hydroxymethyl}amino-methane), approximately 320 mosmol kg−1] and transferred to a perfusion chamber. A PG was impaled with the oilfilled micropipette of the pressure probe while gently holding the PG at the bottom of the chamber with a second pipette. After successful impalement the holding pipette was carefully withdrawn and the impaled PG was lifted from the chamber bottom. The chamber was constantly perfused with bath solutions of different osmolalities adjusted with mannitol (190–500 mosmol kg−1). The turgor pressure was recorded with a chart recorder (Norma Goerz Instruments) or digitized at a sampling frequency of 100 Hz and filtered at 10 Hz cutoff frequency using the Digidata 1200 A/D converter and the Axoscope software (Molecular Devices). During some turgor pressure measurements pressure pulses were applied to calculate the hydraulic conductivity (Lp) from the subsequent pressure relaxation curves or the volumetric elastic modulus (ε) from small pressure increments (Steudle, 1993; Boyer, 1995).

For simultaneous recordings of turgor pressure and membrane potential a new pressure probe was constructed according to Zhu (1996; Fig. 2A). Micropipettes were pulled from glass capillaries containing a glass filament (GC 120F-10, Science Products) with a horizontal pipette puller (Sachs-Flaming PC-84, Sutter Instruments). The tip of the micropipettes was filled with silicon oil (AS-4, Wacker Chemie) and back filled with electrolyte (90 mM K+ acetate, pH 7.3, 10 mM KCl; see Fig. 2A). When mounting the filled micropipette into the pressure probe holder, an Ag/AgCl wire reaching into the electrolyte solution was connected to a voltage amplifier (Y-Science). The electrolyte solution was drawn to the micropipette tip due to the capillary forces between the glass filament and the pipette wall. The electric connection was tested after the micropipette and the reference electrode (1 M KCl) was submersed into the standard bath medium. PGs were impaled as described above and the membrane potential difference (VM) and the turgor pressure were recorded with a two-channel chart recorder.

External pH Measurements

Mature PGs of one anther were resuspended in an unbuffered medium (Med M) containing (in mM): 298 mannitol, 1 KCl, 0.1 CaCl2, 1.6 H3BO3,and the pH was adjusted to 5.6 with tiny amounts of MES or Tris, respectively, if necessary. The PGs were washed three to five times with Med M by short centrifugations to remove the pollenkitt, ions, or other compounds bound to the cell wall. Finally, 1 mL of the pollen suspension was added to 1 mL Med M in the multiport measurement chamber (WPI) housing the reference as well as the pH electrode (Kwik-Tip, WPI). The electrodes were connected to an electrometer (610C, Keithley Instruments) and the data were sampled at 333.3 Hz by an A/D converter (DigiData 1200, Molecular Devices), filtered at 10 Hz cutoff frequency and recorded with the Axoscope 7 software. The quality of the pH electrode was tested before each experiment by measuring solutions with known pH values, giving slopes of 50 to 56 mV per pH unit. The pH value was calculated from the recorded voltage using the calibration curves. The acidification (negative values) or alkalinization rates (positive values) are given as ΔpH min−1. During the measurements the PG suspension was constantly stirred at slow speed and osmolality was changed by adding appropriate volumes of hyper- or hypoosmotic mannitol stock solutions (with all other components as Med M) to give 198 and 398 mM mannitol, respectively, as final concentrations.

PM Isolation, Gel Electrophoresis, and Immunodetection

PGs from 75 flowers were incubated for 15 min in Med M, split to three aliquots with each aliquot incubated for another 15 min in isoosmolar Med M (298 mM mannitol), in hypoosmolar Med M (198 mM mannitol), and in hyperosmolar Med M (398 mM mannitol). Fractions of soluble cytosolic (CF), crude membranes (MF), and PMF proteins were prepared from each pollen aliquot by differential centrifugation followed by discontinuous Suc density gradient centrifugation as described by Pertl et al. (2005, 2009).

Proteins were separated by SDS-PAGE by denaturing protein fractions (10–20 μg protein) in sample buffer (300 mM dithiothreitol, 30% [w/v] SDS, 15% [w/v] glycerol, 180 mM Tris/HCl pH 6.8, bromphenol blue) at room temperature for 15 min and loading onto a discontinuous gel system (Laemmli, 1970) with 4% stacking gel and 10% separation gel (Protean 3 system, Bio-Rad). Proteins were stained with Coomassie Brilliant Blue R-250. The protein concentration was determined using a Lowry DC assay (Bio-Rad).

For immunodetection separated proteins were transferred onto polyvinylidene difluoride membranes (Roth) by electroblotting with 20 V for 1 h (semi dry electrophoretic transfer cell, Bio-Rad) and immunodetection of the PM H+ ATPase and 14-3-3 proteins was performed as described previously (Pertl et al., 2005) with the following antibody concentrations and combinations: MUP5 and MUP15 diluted 1:250 and detected by goat anti-mouse IgG-alkaline phosphatase conjugated (1:5,000 or 1:10,000, Sigma) for 14-3-3 detection. For immunodetection of the PM H+ ATPase the primary antibody was diluted 1:2,500 and secondary antibody goat anti-mouse IgG-alkaline phosphatase was diluted 1:5,000 (Sigma).

PM H+ ATPase Activity

Hydrolysis of ATP by the vanadate-sensitive PM H+ ATPase was monitored by determination of released inorganic phosphate (Ames, 1962) as described in Pertl et al. (2005).

Supplementary Material

ACKNOWLEDGMENTS

We thank Bert de Boer (University of Amsterdam) for his generous gift of antibodies against Hordeum vulgare 14-3-3 proteins.

Footnotes

1This work was supported by the Fond zur Föderung der wissenschaftlichen Forschung (grant nos. P13064-BIO, P17227-B03, and P21298–B03).

[C]Some figures in this article are displayed in color online but in black and white in the print edition.

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Supplemental Data

The following materials are available in the online version of this article.

Supplemental Figure S1. Determination of the hydraulic conductivity (LP).

Supplemental Figure S2. Acidification of the external medium by an active PM H+ ATPase.

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