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Ullrich CI, Guern J. Ion fluxes and pH changes induced by trans-plasmalemma electron transfer and fusicoccin in Lemna gibba L. (strain G1). Planta. 1990;180(3):390-9doi: 10.1007/BF00198791.
Ullrich, C. I., & Guern, J. (1990). Ion fluxes and pH changes induced by trans-plasmalemma electron transfer and fusicoccin in Lemna gibba L. (strain G1). Planta, 180(3), 390-9. https://doi.org/10.1007/BF00198791
Ullrich, C I, and Guern, J. "Ion fluxes and pH changes induced by trans-plasmalemma electron transfer and fusicoccin in Lemna gibba L. (strain G1)." Planta vol. 180,3 (1990): 390-9. doi: https://doi.org/10.1007/BF00198791
Ullrich CI, Guern J. Ion fluxes and pH changes induced by trans-plasmalemma electron transfer and fusicoccin in Lemna gibba L. (strain G1). Planta. 1990 Feb;180(3):390-9. doi: 10.1007/BF00198791. PMID: 24202018.
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Planta. 1990 Feb;180(3):390-9. doi: 10.1007/BF00198791.

Ion fluxes and pH changes induced by trans-plasmalemma electron transfer and fusicoccin in Lemna gibba L. (strain G1).

Planta

C I Ullrich, J Guern

Affiliations

  1. Institut für Botanik der Technischen Hochschule, Schnittspahnstrasse 3, D-6100, Darmstadt, Germany.

PMID: 24202018 DOI: 10.1007/BF00198791

Abstract

During the reduction of extracellular [Fe(CN)6](3-) at the plasmalemma of intact, K(+)-starved Lemna gibba L. fronds, the external medium was acidified and K(+) released, in the absence of inhibitors with rates of 10 e(-)/8.5 H(+)/1.5 K(+) (μmol·(g FW)(-1)·(-1)). In K(+) plants the larger K(+) efflux caused a lag phase in extracellular acidification and a change in rates to 10 e(-)/6 H(+)/4 K(+) and in the presence of CN(-)+salicylhydroxamic acid at pH 5 to 5.2 e(-)/0 H(+)/6.6 K(+). The e(-) transfer was accompanied by a membrane depolarization of up to 100 mV and a cytosolic acidification of about 0.6 pH units, but only in K(+) plants, where the extracellular acidification was smaller. These results indicate that a stimulation of the plasmalemma H(+)-ATPase may be triggered either by a cytosolic acidification or by a strong membrane depolarization. It is concluded that the redox system catalyses only uncoupled e(-) transfer without H(+) transfer across the plasmalemma. The obligatory, but secondary charge compensation is partially achieved by the rapid K(+) release upon membrane depolarization and partially by the activity of the plasma membrane H(+)-ATPase, but not by an e(-)/anion exchange. The extracellular acidification during [Fe(CN)6](3-) reduction is generated by the conversion of a strong trivalent into a strong tetravalent anion. This acidification is caused by changes in the concentration ratio of strong cations to strong anions. Efflux of K(+) and not the production of organic acids or NAD(P)H oxidation is the chemical cause of the measurable cytosolic acidification. Extracellular acidification was inversely correlated with intracellular acidification. Similarly, fusicoccin-induced pH changes were correlated with changes in the strong-ion concentration difference. Extracellular ± FC-dependent acidification and intracellular alkalinization of up to 0.6 pH units were strongly dependent on K(+) fluxes. The ferricyanide-triggered trans-plasmalemma electron-transfer system is an example of how measurable pH changes are the consequence and not the cause of charge-transfer-induced changes in strong-ion fluxes.

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