Calcium sensor kinase activates potassium uptake systems in gland cells of Venus flytraps.

The Darwin plant Dionaea muscipula is able to grow on mineral-poor soil, because it gains essential nutrients from captured animal prey. Given that no nutrients remain in the trap when it opens after the consumption of an animal meal, we here asked the question of how Dionaea sequesters prey-derived potassium. We show that prey capture triggers expression of a K(+) uptake system in the Venus flytrap. In search of K(+) transporters endowed with adequate properties for this role, we screened a Dionaea expressed sequence tag (EST) database and identified DmKT1 and DmHAK5 as candidates. On insect and touch hormone stimulation, the number of transcripts of these transporters increased in flytraps. After cRNA injection of K(+)-transporter genes into Xenopus oocytes, however, both putative K(+) transporters remained silent. Assuming that calcium sensor kinases are regulating Arabidopsis K(+) transporter 1 (AKT1), we coexpressed the putative K(+) transporters with a large set of kinases and identified the CBL9-CIPK23 pair as the major activating complex for both transporters in Dionaea K(+) uptake. DmKT1 was found to be a K(+)-selective channel of voltage-dependent high capacity and low affinity, whereas DmHAK5 was identified as the first, to our knowledge, proton-driven, high-affinity potassium transporter with weak selectivity. When the Venus flytrap is processing its prey, the gland cell membrane potential is maintained around -120 mV, and the apoplast is acidified to pH 3. These conditions in the green stomach formed by the closed flytrap allow DmKT1 and DmHAK5 to acquire prey-derived K(+), reducing its concentration from millimolar levels down to trace levels.

The carnivorous plant Dionaea muscipula actively traps small animals. To this end, it forms leaves that develop into a bilobed capture organ, with the upper surface of the modified leaf equipped with three sensory hairs per lobe. Flies, ants, and spiders, attracted by volatiles, frequently visit the traps, accidentally touching the sensory hairs, thus triggering action potentials (APs) in the trap (1). After two APs have been elicited, the trap closes within a fraction of a second (2). The prey, moving around and trying to escape, repeatedly activates the mechanosensors, which in turn, stimulate the secretion of digestive enzymes from glands lining the inner surface of the trap. The end result is that the prey in Dionaea’s green stomach is completely decomposed, releasing nutrients and minerals that are then available to the plant.

An uptake system for NH4 has already been described (3). However, little is known about the uptake of potassium, which for plants, is a macronutrient required for turgor-based growth and movements (review in ref. 4). From energetic considerations, it has traditionally been proposed that high-affinity K+ uptake in plants is an active process mediated by a K+/H+ symporter, whereas low-affinity, passive uptake is operated by channels (5, 6). The major K+ uptake systems in roots, Arabidopsis thaliana high affinity K+ transporter 5 (AtHAK5) and Arabidopsis K+ transporter 1 (AKT1), were identified by studying Arabidopsis thaliana Transfer-DNA insertion lines, in which these genes are knocked out. AtHAK5 was recognized as the only high-affinity uptake system at external K+ concentrations <10 μM, whereas both AtHAK5 and AKT1 were shown to contribute to K+ acquisition between 10 and 200 μM. At external concentrations >500 μM, AtHAK5 is not relevant, and K+ uptake is dominated by AKT1 (7, 8). Although activation by phosphorylation through the Ca2+-dependent protein kinase complex calcineurin B-like (CBL)/CBL-interacting protein kinases (CIPK) has enabled the characterization of the transport function of AKT1, no detailed electrophysiological characterization of the high-affinity K+ transporter has been possible so far, because HAK5 remains silent in the heterologous expression system of Xenopus oocytes (9). Consequently, the selectivity and regulation of HAK5 are still under debate (10).

Here, we ask the question of how the flytrap acquires prey-derived potassium ions. Our in planta experiments suggested that Dionaea glands operate an insect-induced, dual-affinity potassium uptake system. We, therefore, screened an expressed sequence tag (EST) collection containing RNA from glands of insect- and touch hormone-stimulated flytraps and identified orthologs of AKT1 and AtHAK5, which we name DmKT1 and DmHAK5. Activation of these proteins in Xenopus oocytes by coexpression with a calcium sensor kinase allowed us to provide a detailed electrophysiological characterization of the high- and low-affinity transporters DmHAK5 and DmKT1, respectively. Both proteins, when expressed in oocytes, displayed the gross features as observed in transport studies on whole Dionaea glands.

Results

Flytrap Ingests Prey-Derived Potassium.

To study the capacity of the flytrap for intake of prey-derived potassium, we used an insect powder stock for feeding experiments (11). In a previous study, this well-defined nutrient source was successfully used to trace the intake of amino acids and ammonium (3). The insect fodder paste, which contains a K+ concentration of 30 mM, was applied to the inner trap surface, whereupon the sensory hairs were stimulated to close the capture organ and commence secretion of digestive fluid. This protocol, designed to mimic living prey, caused the two trap lobes to form a hermetically sealed green stomach (2). By sampling the nutrient intake organs and removing any remaining fodder paste and stomach contents, we determined their time-dependent changes in potassium content. When monitoring the total trap K+ content by inductively coupled plasma MS, we found that the level of this major plant cation started rising 4–6 h after initiating feeding and reached a steady state at 12–24 h. The higher level lasted for at least 2–3 d (Fig. 1). The steady-state K+ content of the fed traps was about two times that of control traps (t = 0 and 2 h after feeding). These results indicate that Dionaea has the capacity to take up and store prey-derived potassium in the capture organ. To confirm this finding and study the potassium intake at a higher resolution, we complemented the insect paste with the K+-tracer Rb+ at concentrations of 30 (Fig. 1), 3, and 0.3 mM (Fig. S1). Apart from starting from a zero level, the Rb+ concentration of traps showed the same kinetics of increase as that determined for K+. Rubidium uptake was already visible at a food stock concentration of 0.3 mM and increased with increasing Rb+ concentration (Fig. S1).

Fig. 1.

K+ uptake in Dionaea traps. (A) Traps were fed with standardized insect powder, and both time-dependent K+ and Rb+ uptakes were analyzed. After 12 h of digestion, both the K+ and Rb+ concentrations in fed traps doubled compared with unfed traps (time = 0). (B) Using MIFE experiments with unstimulated (black) and COR-treated (red) Dionaea traps, K+ influxes were measured in response to the indicated external K+ concentrations. High-affinity K+ influx was obtained in COR-treated traps only. After the normalization of K+ fluxes to 1 at 1 mM K+, data points could be best fitted with a Michaelis–Menten function (solid line), revealing a Km value of 0.06 ± 0.01 mM (n ≥ 7; mean ± SD). (C) K+ uptake triggered membrane depolarizations in Dionaea glands on application of 0.6 or 2 mM external K+. (D) High- and low-affinity response curves of gland cell membrane depolarizations (red and black, respectively) and normalized currents (blue) of DmKT1/DmHAK5/CBL9/CIPK23-coexpressing oocytes at various external K+ concentrations. Curves in the two concentration ranges were independently fitted with Michaelis–Menten equations to obtain the indicated half-maximal depolarizations (EC50 values; mean membrane depolarization ± SD; 3 ≤ n ≤ 8).

Gland K+ Uptake Displays Both Low- and High-Affinity Transport Components.

To study the K+ uptake, we monitored the K+ fluxes into the gland-covered inner trap surface using the vibrating ion-selective electrode technique microelectrode ion flux measuring (MIFE) (12, 13). Single-trap lobes were fixed to a chamber, and ion-selective microelectrodes were placed close to the trap surface, which is densely packed with about 37,000 glands per trap (2), monitoring K+ fluxes under different external K+ concentrations. Unstimulated traps did not take up any external K+ in the high-affinity range. In contrast, when traps were pretreated with the touch hormone mimic coronatine [COR; a substitute for insect stimulation (2)], macroscopic inward K+ fluxes were detected (Fig. 1 and Fig. S2). When we increased K+ concentration stepwise from 0.01 to 1 mM with media buffered to pH 4, electrodes registered inward fluxes of up to 200 nmol m−2 s−1 in COR-stimulated traps. Fluxes tended to saturate, reaching a steady state at ∼500 µM external K+ (Fig. 1 and Fig. S2). By fitting a Michaelis–Menten equation to the K+ dose–response curve in this low-concentration range, a half-saturation concentration of about 60 µM was calculated (Fig. 1). This apparent Km value is in line with a high-affinity potassium uptake system (ref. 14 and references therein). Such a system requires energy from either an electrical and/or a chemical gradient. Uphill carrier transport of many solutes is coupled to the downhill movement of protons (15–17). When we shifted the pH from 4 to 8, COR-induced potassium fluxes were completely suppressed, indicating that high-affinity trap K+ uptake is driven by a proton gradient (Fig. S2).

Increasing the external K+ concentration to values much higher than the Km of the high-affinity transport further increased the fluxes. At 10 mM K+, inward fluxes as high as or even above 1,000 nmol m−2 s−1 (10 times the maximum value of the high-affinity transport) were detected. These high-capacity fluxes point to the presence of a low-affinity transport system in addition to the low-capacity, high-affinity component (Fig. S2). The fact that even unstimulated traps respond to high external K+ concentrations points to a basal expression of the low-affinity component compared with the high-affinity uptake system.

Extracellular electrodes provide a noninvasive assay of trap K+ fluxes, but they do not report the membrane potential of the cells engaged with K+ transport, a quantity required for thermodynamic considerations. Influx of potassium ions and protons into gland cells is expected to depolarize their membrane potential. To monitor the predicted membrane response of gland cells, we inserted sharp impalement electrodes into cells of layer 1 or 2 of the dome-shaped glands. At pH 4 and 0.1 mM external K+, we recorded a resting potential around −140 mV for both insect and COR-stimulated gland cells (cf. 3). The addition of 2 mM K+ depolarized the membrane potential of stimulated glands (Fig. 1, red line). Given a gland cell cytoplasmic potassium load of 100 mM and a green stomach concentration above 1 mM K+, an electrical force of ≤−120 mV would theoretically suffice to drive K+ influx through an acid pH-activated potassium channel (18). At an external potassium level lower than 1 mM, however, the gland cell membrane potential would not be able to energize transport against a potassium concentration gradient greater than 100-fold if it was mediated by a channel-like mechanism. However, the application of 0.6 mM K+ at pH 4 still resulted in a potassium-dependent depolarization in the same range. This finding points toward a high-affinity K+ transport mechanism, a system that is not only energized by the membrane potential gradient (Fig. 1, black line). By plotting the depolarization against the applied K+ concentration, a biphasic character becomes evident (Fig. 1, red). The high-affinity component in K+ uptake reaches its half-maximum activity at 0.48 ± 0.38 mM, whereas the low-affinity transport does so at 65.48 ± 33.7 mM external K+ (Fig. 1). Performing the same experiment with unstimulated gland cells (Fig. 1, black), we find almost no depolarization in the high-affinity range. When we further increase the K+ concentration to the low-affinity range, a distinct depolarization in unstimulated gland cells becomes obvious. This investigation points to a different expressional regulation of high- and low-affinity transporters during digestion.

Thus, our impalement electrode recordings together with the MIFE measurements indicate that gland cells of insect and COR-stimulated traps possess both a high-affinity, pH-dependent K+/H+ symport and a low-affinity, high-capacity K+ transport system.

Stimulated Glands Express AKT-Like Potassium Channel and HAK-Type K+-Transporter Genes.

To elucidate the genes encoding Dionaea’s gland potassium uptake system, we searched an EST database (cf. 3, 19, and 20), identifying the AKT1-like, Shaker-type potassium channel ortholog DmKT1 and the HAK-type transporter DmHAK5 as potential candidates. Both proteins were found to be expressed and up-regulated in digesting glands of the Venus flytrap. Detailed information is in and Fig. S3 .

Dionaea’s K+ Transport Requires Activation by a Calcium Signaling Kinase.

Xenopus laevis oocytes are widely used to express genes from different taxa. The function of Arabidopsis AKT1 when expressed in this system depends on phosphorylation by a calcium sensor kinase of the CBL/CIPK type (21, 22). We also found orthologs of CIPK23 and CBL9 expressed in Dionaea. In contrast to AKT1 (21, 22), however, HAK5 transporters do not seem to be functionally expressed in this animal expression system, which is plant background-free. Consequently, no detailed electrophysiological characterization of HAK transporters has been possible (9, 23). Given that, in Arabidopsis, the AKT1 potassium channel function depends on a CBL/CIPK pair, we reasoned that, in Dionaea, AKT1 and probably, HAK5 orthologs could also depend on a similar calcium sensor kinase complex. Indeed, expression of DmKT1-mediated macroscopic inward K+ currents is only in the presence of the Arabidopsis CBL9/CIPK23 pair, which also activates its Arabidopsis ortholog AKT1 (Fig. S4 ) (21, 22).

Regarding HAK-type transporters, we first performed an experiment similar to that in the work by Kim et al. (9), which studied a high-affinity KUP/HAK/KT family member. Just like in the work by Kim et al. (9), we were not able to observe macroscopic K+ currents in Xenopus oocytes expressing DmHAK5 cRNA alone (Fig. 2). However, we then expressed DmHAK5 together with various CBL/CIPK combinations and found substantial inward currents (Fig. 2) when using the CBL9/CIPK23 pair and K+-containing buffers at a pH of 4. The requirement of pH 4 is not surprising given that, on prey processing, Dionaea’s stomach acidifies. The notion that both DmHAK5 and DmKT1 may interact with the CIPK23 was supported by bimolecular fluorescence complementation-based protein–protein interaction assays (Fig. S4 ) (cf. 24). Thus, the same calcium sensor kinase, CIPK23, regulates the transport function of both DmKT1 and DmHAK5. We conclude that the calcium-dependent kinase acts as a key regulator for both the low- and high-affinity potassium uptakes in Dionaea glands.

Fig. 2.

Transport activation of DmHAK5. (A) Normalized current response recorded at −140 mV of Xenopus oocytes injected with H2O, cRNA of DmHAK5, or cRNA of DmHAK5 supplemented with CBL9/CIPK23. Macroscopic potassium currents were only detectable in DmHAK5/CBL9/CIPK23-coexpressing oocytes in solutions containing 2 mM potassium (n ≥ 6; mean ± SD). (B) Typical whole-oocyte currents recorded at −60 mV of an H2O-injected (black) and a DmHAK5/CBL9/CIPK23-expressing (red) Xenopus oocyte. Addition of 2 mM K+ resulted in macroscopic inward currents of ∼400 nA only with DmHAK5-expressing oocytes. The dotted line represents zero current.

DmKT1 Is a K+-Selective Channel with Voltage- and pH-Dependent Gating.

As with other members of the Shaker-like K+-channel family, DmKT1 is classified as a voltage-dependent inward-rectifying K+ channel. When the AKT1 ortholog from Dionaea was coexpressed with CBL9/CIPK23, a typical hyperpolarization-activated, inward-rectifying K+-channel activation was observed under 100 mM external K+ (Fig. S4 ). Animals contain potassium and sodium at about similar concentrations (25, 26). When prey are decomposed in Dionaea’s green stomach, the K+ uptake system is exposed to both monovalent cations. We therefore investigated the cation selectivity of the flytrap AKT1 ortholog. Oocytes were incubated with solutions containing Li+, Na+, K+, Rb+, Cs+, NH4+, or N-methyl-d-glucamine (NMDG+) at 100 mM concentration. However, DmKT1-mediated cation inward currents were observed in potassium-based buffers only (Fig. 3). On a 10-fold change in bath K+ concentration from 10 to 100 mM, a near-Nernstian shift in reversal potential (53.80 ± 1.06 mV; n = 6 ± SD) was observed, indicating that DmKT1 is a K+-selective channel. With the acidification during prey digestion, this K+ channel is additionally confronted with a high external H+ concentration. When oocytes were superfused with 100 mM KCl, a distinct increase in K+ inward current was observed when the pH was lowered stepwise from 6 to 3 (Fig. 3 ). Interestingly, any shift in reversal potential in response to this change in proton concentration by three orders of magnitude was insignificant from zero (−0.43 ± 3.06 mV; n = 6 ± SD; P > 0.5 by one-way ANOVA). This result documents that H+ is not transported by the channel. A Boltzmann analysis of DmKT1 channel activity at an external pH of 6 revealed a voltage dependence with a half-maximal activation potential (V1/2) of −129.64 ± 3.06 mV. Increasing the external H+ concentration shifts this potential to more positive values, reaching a V1/2 of −78.29 ± 2.35 mV at pH 3 (Fig. 3). These findings are in line with an acid-induced shift in the open probability (PO) of the channel (cf. 27).

Fig. 3.

Selectivity and pH dependency of DmKT1. (A) Currents recorded at −140 mV of DmKT1/CBL9/CIPK23-expressing oocytes in the presence of bath solutions containing various monovalent cations (each 100 mM). Large cation influx was only obtained with potassium in the external bath solution (n = 4; mean ± SD). (B) Inward K+ currents elicited by a DmKT1/CBL9/CIPK23-expressing Xenopus oocyte markedly increased on acidification of the external solution (Vm = −100 mV). Exchanging 100 mM external Li+ for 100 mM K+ at pH 6 resulted in potassium influx, which was enhanced by increasing the external H+ concentration. The dotted line represents zero currents. (C) Normalized currents of DmKT1/CBL9/CIPK23-expressing Xenopus oocytes at −140 mV. Stepwise acidification from pH 6 to 3 increased the potassium currents through DmKT1 (n = 6; mean ± SD). (D) The relative open probability (rel. PO) of DmKT1-expressing oocytes at the indicated H+ concentrations was plotted against the applied test voltage. Note the prominent positive shift of the half-maximal activation potential (V1/2) with increasing acidification. The data points were fitted with a Boltzmann function (solid lines; n = 6; mean ± SD).

DmHAK5 Is an H+-Driven K+ Transporter.

The fact that even rubidium, which is commonly used as a potassium tracer, does not permeate DmKT1 (Fig. 3) raises questions about the transport of rubidium in experiments with insect powder feeding (Fig. 1 and Fig. S1). We therefore superfused oocytes expressing DmHAK5 and CBL9/CIPK23 with a sorbitol-based solution of pH 4 supplemented with 2 mM Li+, Na+, K+, Rb+, Cs+, NH4+, or NMDG+ (Fig. 4 ). In the presence of potassium and rubidium ions, DmHAK5-mediated inward currents were of similar amplitudes, whereas the currents with caesium and ammonium as charge carriers were reduced by 65–50%. Lithium, sodium, and NMDG ions at 2 mM concentration did not evoke DmHAK5-mediated currents (Fig. 4 ).

Fig. 4.

Selectivity and pH dependency of DmHAK5. Xenopus oocytes were either injected with H2O (control) or cRNA of DmHAK5/CBL9/CIPK23 (DmHAK5). (A) Representative current recordings at −60 mV of a control (black) and a DmHAK5-expressing (red) Xenopus oocyte in response to 2 mM Li+, Na+, K+, Rb+, Cs+, NH4+, or NMDG+ (as indicated using sorbitol-based solutions). Both K+ and Rb+ resulted in macroscopic inward currents with DmHAK5-expressing oocytes. Application of NH4+ and Cs+ induced weaker DmHAK5-mediated inward currents. The dotted line represents zero current. (B) Average results from experiments as shown in A, except that the holding potential was −140 mV (n = 7; mean ± SD). (C) Normalized steady-state currents of Xenopus oocytes injected with DmHAK5 were recorded at −140 mV in response to sorbitol- or Na+-based solution (200 mOsm/kg). Addition of 2 mM K+ resulted in identical K+ influx irrespective from the presence or absence of sodium in the bath solution (n = 7; mean ± SD). (D) ISS recorded at −140 mV with oocytes injected with either H2O (gray bars) or DmHAK5 (red bars) in the presence of 100 mM K+ at different pH values (as indicated; n = 5; mean ± SD). Compared with control oocytes, K+ currents increased at pH values ≤5.

In the green stomach, the selective K+ uptake will decrease the external K+ concentration to very low levels, but Na+ might remain high. Consequently, we asked whether DmHAK5 would still be impermeable to Na+ under such conditions and monitored the currents of DmHAK5-expressing oocytes at a Na+ concentration 50 times higher compared with the K+ concentration of 2 mM. Currents were the same as those recorded during replacement of Na+ by sorbitol (Fig. 4). Also, in the absence of K+, currents were small and similar in amplitude, regardless of whether 100 mM Na+ or sorbitol was present. This finding shows that, even under conditions of high sodium background, which might be found in the green stomach, DmHAK5 remains Na+-impermeable and that transporter activity is unaffected by Na+.

As mentioned above, gland acid secretion can lower the pH in the green stomach to a value of 3 or even lower (2), and MIFE experiments displayed a pH dependency of K+ transport. To study these effects in more detail, we exposed oocytes expressing the activated DmHAK5 to a saturating K+ concentration, while varying the H+ concentration. Compared with control oocytes, an increasing K+ current at pH ≤ 5 was observed (Fig. 4). This finding is well in line with the in planta recordings and supports the hypothesis of an H+-driven, high-affinity K+ symport.

DmKT1 Has High Capacity and Low Affinity, Whereas DmHAK5 Has Low Capacity and High Affinity.

To explore whether both Dionaea gland K+ uptake systems act complementary to each other, we analyzed their affinity to their major substrates. With oocytes expressing the calcium sensor kinase-activated DmKT1 or DmHAK5, we stepwise increased the external potassium concentration in buffers of pH 4. In the presence of 5 mM external K+ and at −140 mV, DmKT1-expressing oocytes supported an inward current of 0.15 ± 0.06 µA, which increased up to 6.42 ± 0.32 µA when the K+ concentration was raised to a maximum of 100 mM (Fig. S5). A plot of current against [K+] could be fitted with a Michaelis–Menten function, with a Km value of 108.29 ± 7.34 mM (Fig. 5).

Fig. 5.

Biophysical analysis of DmKT1- and DmHAK5-mediated K+ currents at varying extracellular K+ concentrations. (A) Dose–response curve of DmKT1/CBL9/CIPK23-expressing Xenopus oocytes at −140 mV. The ionic strength of the solutions with varying K+ concentrations was adjusted to 100 mM with Li+. The saturation curve could be best fitted with a Michaelis–Menten equation (solid line), documenting a Km value of 108.29 ± 7.34 mM for DmKT1 (n = 5; mean ± SD). (B) Dose–response curve of DmHAK5/CBL9/CIPK23-expressing Xenopus oocytes clamped to a membrane potential of −140 mV. The Michaelis–Menten fit revealed a Km value of 127.38 ± 2.77 µM for DmHAK5 (n = 6; mean ± SD). (C) GK/V relationship of DmKT1-expressing oocytes in a K+ concentration range from 100 to 5 mM. Data points were normalized to GK at −140 mV in 100 mM K+ and fitted with a Boltzmann function. Decreasing the potassium concentration leads to a reduction in the cord conductance but not a change of the voltage dependence of the relative open probability (see also Fig. S5) (n = 5; mean ± SD). (D) The relative maximal cord conductance was calculated with the equation: GK−max = GK−max(X mM)/GK−max (100 mM). Data points were plotted against the applied K+ concentration and fitted with a Michaelis–Menten equation. Note that GK−max increased with increasing potassium concentrations with a half-maximal activity (K0.5) of 34 mM (n = 5 ± SD).

Likewise, a rising inward current was observed when superfusing DmHAK5-expressing oocytes with increasing K+ concentrations under similar conditions. However, the dose–response curve in this case could be fitted with a Michaelis–Menten equation with a Km value of 127.38 ± 2.77 µM (Fig. 5) (850 times lower than that of DmKT1). These features and the temperature dependence ( and Fig. S6 ) of DmHAK5 are well in line with a low-capacity, high-affinity, proton-driven K+ transporter, which was observed by MIFE and impalement observations of whole Dionaea glands. When we coexpressed DmKT1 together with DmHAK5 in oocytes, we observed a biphasic K+ uptake (Fig. 1, blue). This combined behavior of the two transporters is reminiscent of the gland K+ response (Fig. 1, red).

Low Extracellular Potassium Leads to Decreased Conductance of DmKT1.

To gain additional insights into the molecular basis of channel activity at different external K+ concentrations, we performed a quantitative comparison of DmKT1 activation curves by analyzing the channel’s cord conductance GK (cf. 28) (). This quantity was shown to be a good estimation for the voltage-dependent channel conductance in Arabidopsis AKT1 and KAT1. Plots of GK vs. voltage, obtained at various K+ concentrations, were well-described by Boltzmann functions (Fig. 5). They revealed that GK of DmKT1 decreased on lowering the external K+ concentration. Decreasing the external K+ concentrations from 100 to 5 mM, the cord conductance decreased by nearly 82% (Fig. 5). The deduced maximal cord conductance (GK−max), which was derived from the Boltzmann fittings, was plotted against the corresponding K+ concentrations (Fig. 5). The resulting saturation curve could be best described by a Michaelis–Menten equation and yielded a half-maximal value (K0.5) of 34 mM external potassium. How can this behavior be explained? Using biophysical approaches, it had been shown that the Arabidopsis potassium channel KAT1 is K+-sensitive in the low millimolar range (K0.5 of 1.4 mM), whereas Arabidopsis AKT1 is K+-sensitive at higher concentrations (K0.5 of 16.2 mM) (28, 29). In both studies, the inhibition of KAT1 and AKT1 has been associated with a pore collapse at low external K+ concentrations. We found that the open probability of DmKT1 is only weakly affected by K+ concentration changes ( and Fig. S5). Therefore, the major GK reduction of DmKT1 is also most likely caused by the reduction of the number of activatable channels at moderate external potassium concentrations. The higher sensitivity to low external K+ of DmKT1 compared with Arabidopsis K+ channels very likely represents an adaption to the needs within the Dionaea digestive organ. By inactivating DmKT1 under conditions of outward-directed K+ driving forces, Dionaea prevents K+ leakage from the gland cells.

Discussion

The carnivorous Darwin plant Dionaea is equipped with a unique sensory system and information management through APs to capture prey and then, digest its nutrients (30). Because Dionaea is a nonmodel, nontransformable plant, we used a recently established gain-of-gene function approach (3, 31) and revealed the trap transporters engaged in potassium uptake. We document that transcription of a Dionaea HAK5-type transporter in glands is induced by prey capture and the presence of jasmonate-type touch hormones. In addition to DmHAK5, we found that a Shaker-type DmKT1 channel is also expressed in Dionaea glands. We cloned and expressed both DmHAK5 and DmKT1 in the Xenopus oocytes system, which is free of any plant background. Nevertheless, in this heterologous system, both transporters have the same fingerprint as they do in their native flytrap.

In these specialized organs, like in roots of the model plant A. thaliana, the HAK5 K+ transporter and AKT1 K+ channel represent the two major complementary systems for K+ uptake (8, 14). Interestingly, we found that the DmHAK5 K+/H+ cotransporter is posttranslationally activated by the same CBL/CIPK complex as the AKT1-type Shaker channel (21). The HAK-type transporter is apparently the only system capable of operating at micromolar K+ concentrations (14). The first high-affinity K+-transporter HAK1 was cloned from Schwanniomyces occidentalis, an ascomycete yeast that is able to grow in a nutrient-poor environment and can accumulate potassium when the available external concentrations are in the low submicromolar range (32). Dionaea faces a very similar situation, and it is able to obtain K+ from the captured animal nutrient source, even when concentrations are at trace levels.

During digestion of Dionaea’s prey, acidification in the external stomach shifts the open probability of DmKT1 to more positive values, thus allowing this channel to activate. Given that the cytoplasm of the gland cells contains 100 mM potassium and that the membrane potential of a digesting Dionaea gland is about −120 mV, this K+-selective channel can acquire external K+ passively down to a value of 1 mM. Below this concentration, the K+ flux would be reversed if the channels would remain open, the result of the outwardly directed electrochemical driving force. Nonetheless, such K+ leakage is prevented by a reduction of channel activity under low external K+.

In this study, we were able to activate an HAK-type transporter for the first time, to our knowledge, in Xenopus oocytes. We found that DmHAK5 is of low selectivity, transporting K+ = Rb+ ≥ NH4+ ≥ Cs+. Interestingly, Na+ is neither a substrate nor a modulator of the HAK5-type transporter in Dionaea. The influence of this cation without having the transporter functionally expressed in oocytes was still unclear and a matter of debate (33–38).

By reporting a Km of 127 µM, we clearly classify DmHAK5 as a high-affinity transporter that is active at K+ concentrations too low for K+ uptake by DmKT1. During the absorption of a prey’s mineral deposits, K+ concentration drops to 10 µM, which leads to the question of how DmHAK5 energizes an uphill transport against a 10,000-fold concentration gradient under the assumption of a 100 mM cytosolic K+. To overcome such a high gradient, a passive K+ channel would only generate an influx at a membrane potential (electrical potential) more negative than −240 mV. However, the membrane potential of gland cells, even during prey digestion and nutrient uptake, is maintained around −120 mV (cf. this study and 3). To overcome this problem, DmHAK5, acting as a K+/H+ symporter, uses the chemical potential of the proton in addition to the electrical potential. Assuming a cytosolic pH of the gland cells of 7 and a pH of 3 or lower for the prey-digesting acidic fluid in the green stomach, the proton-motive force would add the equivalent of an additional −240 mV to the membrane potential. From thermodynamic considerations, the combined force would allow the flytrap to accumulate K+ more than 100,000-fold. Other than this thermodynamic consideration and the pH dependence of DmHAK5-mediated transport, final proof for K+/H+ coupling and stoichiometry requires measurements on the K+- and H+-dependent shift in reversal potential.

Thus, both proteins are activated by the same calcium-dependent kinase and work together to provide an orchestrated acquisition of potassium. With the high capacity of DmKT1 and the high affinity of DmHAK5, this K+ uptake module within the green stomach is able to sequester the prey-derived potassium rapidly when the potassium concentration is relatively high as well as reduce it to very low remnant levels.

Methods

Cloning of DmKT1 and DmHAK5.

In brief, we used an available EST database from D. muscipula (19) and identified coding sequences related to potassium transporter homologs. Putative transporter genes were cloned into oocyte expression vectors (39), and cRNAs were injected into Xenopus oocytes for functional analysis. Detailed information is in .

Plant Material and Tissue Sampling.

D. muscipula plants were purchased from CRESCO Carnivora and grown in plastic pots at 22 °C in a 16-h light/8-h dark photoperiod. The material for the expression analyses was treated as described elsewhere (3).

Feeding Experiments.

For rubidium and potassium uptake measurements, traps were fed with 20 mg insect powder and dispensed in 100 μL water or RbCl solution to obtain the desired Rb+ concentration. Insect powder was produced from adult moths of Vanessa cardui (Lep.: Nymphalidae), which had K+ content that was ∼30 mM; 24 h after feeding, traps were harvested, the remaining insect material was removed, and the plant tissue was completely dried. Subsequently, the ground plant powder was digested with HNO3 in a pressure ashing device (Seif). Samples diluted with H2O were analyzed by inductively coupled plasma optical emission spectroscopy (JY 70 Plus; Devision d’Instruments S.A.).

Expression Analyses.

RNA was separately isolated from each sample and transcribed into cDNA using M-MLV Reverse Transcriptase (Promega). Quantifications of the actin transcript DmACT (GenBank accession no. KC285589) and DmHAK5 transcript were performed by real-time PCR as described elsewhere (40). DmHAK5 transcripts were normalized to 10,000 molecules DmACT.

In a second approach, transcript levels of DmHAK5 and DmKT1 after stimulation with insects and COR were measured with RNA sequencing (RNA-seq). RNA-Seq by expectation-maximization (RSEM) (10.1186/1471-2105-12-323) was used to quantify expression levels based on an assembled transcriptome. DNA-sequencing (DNA-Seq) (10.1186/gb-2010-11-10-r106) was used to normalize between samples and experiments for the final visualization.

Noninvasive Ion Flux Measurements.

Net K+ fluxes were measured using noninvasive MIFE technique (University of Tasmania). The theory of noninvasive MIFE measurements and all specific details of microelectrode fabrication and calibration are described in and prior publications (12, 13, 41).

Intracellular Measurements.

Before measurements, the lobe of a cut trap was glued to the bottom of a chamber and left for recovery (30 min) in a standard solution containing 0.1 mM KCl, 10 mM CaCl2, and 150 mM MES adjusted with Tris to pH 4. Osmolarity was kept at 240 mOsm/kg with d-sorbitol when needed. KCl supplementing standard solution was at concentrations of 0.15, 0.3, 0.6, 3, 6, 30, 60, and 120 mM. Detailed information is in .

Oocyte Recordings.

Oocyte preparation and cRNA generation and injection have been described elsewhere (3, 24, 28, 42). In two-electrode voltage-clamp studies, oocytes after 2 or 3 d of expression were perfused with ND 96-based solutions. Detailed information regarding solutions, pulse protocols, and data analysis is in .