Arabidopsis HAK5 under low K<sup>+</sup> availability operates as PMF powered high-affinity K<sup>+</sup> transporter.

Maierhofer, Tobias; Scherzer, Sönke; Carpaneto, Armando; Müller, Thomas D; Pardo, Jose M; Hänelt, Inga; Geiger, Dietmar; Hedrich, Rainer · Nat Commun · 2024

basic_science · Level V

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Abstract

Plants can survive in soils of low micromolar potassium (K<sup>+</sup>) concentrations. Root K<sup>+</sup> intake is accomplished by the K<sup>+</sup> channel AKT1 and KUP/HAK/KT type high-affinity K<sup>+</sup> transporters. Arabidopsis HAK5 mutants impaired in low K<sup>+</sup> acquisition have been identified already more than two decades ago, the molecular mechanism, however, is still a matter of debate also because of lack of direct measurements of HAK5-mediated K<sup>+</sup> currents. When we expressed AtHAK5 in Xenopus oocytes together with CBL1/CIPK23, no inward currents were elicited in sufficient K<sup>+</sup> media. Under low K<sup>+</sup> and inward-directed proton motive force (PMF), the inward K<sup>+</sup> current increased indicating that HAK5 energetically couples the uphill transport of K<sup>+</sup> to the downhill flux of H<sup>+</sup>. At extracellular K<sup>+</sup> concentrations above 25 μM, the initial rise in current was followed by a concentration-graded inactivation. When we replaced Tyr450 in AtHAK5 to Ala the K<sup>+</sup> affinity strongly decreased, indicating that AtHAK5 position Y450 holds a key for K<sup>+</sup> sensing and transport. When the soil K<sup>+</sup> concentration drops toward the range that thermodynamically cannot be covered by AKT1, the AtHAK5 K<sup>+</sup>/H<sup>+</sup> symporter progressively takes over K<sup>+</sup> nutrition. Therefore, optimizing K<sup>+</sup> use efficiency of crops, HAK5 could be key for low K<sup>+</sup> tolerant agriculture.

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