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First published online June 30, 2006; 10.1104/pp.106.082701

Plant Physiology 141:1494-1507 (2006)
© 2006 American Society of Plant Biologists

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WHOLE PLANT AND ECOPHYSIOLOGY

Rapid, Futile K+ Cycling and Pool-Size Dynamics Define Low-Affinity Potassium Transport in Barley1

Mark W. Szczerba, Dev T. Britto and Herbert J. Kronzucker*

Department of Life Sciences, University of Toronto, Toronto, Ontario, Canada M1C 1A4

Using the short-lived radiotracer 42K+, we present a comprehensive subcellular flux analysis of low-affinity K+ transport in plants. We overturn the paradigm of cytosolic K+ pool-size homeostasis and demonstrate that low-affinity K+ transport is characterized by futile cycling of K+ at the plasma membrane. Using two methods of compartmental analysis in intact seedlings of barley (Hordeum vulgare L. cv Klondike), we present data for steady-state unidirectional influx, efflux, net flux, cytosolic pool size, and exchange kinetics, and show that, with increasing external [K+] ([K+]ext), both influx and efflux increase dramatically, and that the ratio of efflux to influx exceeds 70% at [K+]ext ≥ 20 mM. Increasing [K+]ext, furthermore, leads to a shortening of the half-time for cytosolic K+ exchange, to values 2 to 3 times lower than are characteristic of high-affinity transport. Cytosolic K+ concentrations are shown to vary between 40 and 200 mM, depending on [K+]ext, on nitrogen treatment (NO3 or NH4+), and on the dominant mode of transport (high- or low-affinity transport), illustrating the dynamic nature of the cytosolic K+ pool, rather than its homeostatic maintenance. Based on measurements of trans-plasma membrane electrical potential, estimates of cytosolic K+ pool size, and the magnitude of unidirectional K+ fluxes, we describe efflux as the most energetically demanding of the cellular K+ fluxes that constitute low-affinity transport.


1 This work was supported by grants from the Natural Sciences and Engineering Research Council of Canada.

The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Herbert J. Kronzucker (herbertk{at}utsc.utoronto.ca).

Article, publication date, and citation information can be found at www.plantphysiol.org/cgi/doi/10.1104/pp.106.082701.

* Corresponding author; e-mail herbertk{at}utsc.utoronto.ca; fax 416–287–7642.

Received April 27, 2006; returned for revision June 1, 2006; accepted June 17, 2006.




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