Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1986 Sep;82(1):316–323. doi: 10.1104/pp.82.1.316

Stimulation of Weak Acid Uptake and Increase in Cell Sap pH as Evidence for Fusicoccin- and K+-Induced Cytosol Alkalinization 1

Maria Teresa Marrè 1,2, Giulia Romani 1,2, Mario Bellando 1,2, Erasmo Marrè 1,2
PMCID: PMC1056110  PMID: 16665014

Abstract

In maize root segments fusicoccin induced a consistent increase in cell sap pH (taken as representative of vacuolar pH). This effect was markedly enhanced by the presence of K+ in the medium, whereas in the absence of fusicoccin K+ did not significantly influence cell sap pH. Treatment with a weak acid at 2 mm concentration inhibited the uptake of a different (14C-labeled) weak acid fed at a lower concentration, thus suggesting that acidification of the cytoplasm inhibits weak acid uptake. Fusicoccin and K+ increased the rate of uptake of 5,5-dimethyloxazolidine-2,4-dione, butyric acid, or isobutyric acid slightly when fed separately, strongly when fed in combination. The synergism between fusicoccin and K+ in stimulating weak acid uptake was parallel to that observed for the stimulation of H+ extrusion. Application of the weak acid distribution method to a condition of `quasi-equilibrium' indicated that fusicoccin induces a cytosolic pH increase of about 0.14 unit. These results are interpreted as providing circumstantial evidence that fusicoccin- and K+- induced stimulation of H+ extrusion led to an alkalinization of the cytosol, and that other early metabolic responses, such as an increase in malate level, are a consequence of the increase in cytosolic pH.

Full text

PDF
316

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Davies D. D. Control of and by pH. Symp Soc Exp Biol. 1973;27:513–529. [PubMed] [Google Scholar]
  2. Haschke H. P., Lüttge U. Stoichiometric Correlation of Malate Accumulation with Auxin-dependent K-H Exchange and Growth in Avena Coleoptile Segments. Plant Physiol. 1975 Nov;56(5):696–698. doi: 10.1104/pp.56.5.696. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Marrè E., Ballarin-Denti A. The proton pumps of the plasmalemma and the tonoplast of higher plants. J Bioenerg Biomembr. 1985 Feb;17(1):1–21. doi: 10.1007/BF00744985. [DOI] [PubMed] [Google Scholar]
  4. Rasi-Caldogno F., Pugliarello M. C. Fusicoccin stimulates the H+-ATPase of plasmalemma in isolated membrane vesicles from radish. Biochem Biophys Res Commun. 1985 Nov 27;133(1):280–285. doi: 10.1016/0006-291x(85)91872-8. [DOI] [PubMed] [Google Scholar]
  5. Romani G., Marrè M. T., Bellando M., Alloatti G., Marrè E. H extrusion and potassium uptake associated with potential hyperpolarization in maize and wheat root segments treated with permeant weak acids. Plant Physiol. 1985 Nov;79(3):734–739. doi: 10.1104/pp.79.3.734. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. WADDELL W. J., BUTLER T. C. Calculation of intracellular pH from the distribution of 5,5-dimethyl-2,4-oxazolidinedione (DMO); application to skeletal muscle of the dog. J Clin Invest. 1959 May;38(5):720–729. doi: 10.1172/JCI103852. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES