Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1997 Apr;113(4):1419–1426. doi: 10.1104/pp.113.4.1419

Characterization of a Light-Controlled Anion Channel in the Plasma Membrane of Mesophyll Cells of Pea.

JTM Elzenga 1, E Van Volkenburgh 1
PMCID: PMC158266  PMID: 12223683

Abstract

In leaf mesophyll cells of pea (Pisum sativum) light induces a transient depolarization that is at least partly due to an increased plasma membrane conductance for anions. Several channel types were identified in the plasma membrane of protoplasts from mesophyll cells using the patch-clamp technique. One of these was an anion channel with a single-channel conductance of 32 picasiemens in symmetrical 100/100 KCl solutions. In asymmetrical solutions the reversal potential indicates a high selectivity for Cl- over K+ at high cytoplasmic Cl-. At negative membrane voltages the channel openings were interrupted by very short closures. In the open channel conductance several substrates were identified. At a cytoplasmic negative logarithm of Ca concentration higher than 6.3, no channel openings were observed. When the protoplast was illuminated in the cell-attached configuration, at least one channel type had a higher opening probability. This channel can tentatively be identified as the above-described anion channel based on conductance and the characteristic short closures at negative membrane potentials. This light activation of the 32-picasiemen anion channel is a strong indication that this channel conducts the light-induced depolarizing current. Because channel activity is strongly Ca2+-dependent, a role of cytoplasmic Ca2+ concentration changes in the light activation of the conductance is discussed.

Full Text

The Full Text of this article is available as a PDF (802.2 KB).

Selected References

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

  1. Barry P. H. JPCalc, a software package for calculating liquid junction potential corrections in patch-clamp, intracellular, epithelial and bilayer measurements and for correcting junction potential measurements. J Neurosci Methods. 1994 Jan;51(1):107–116. doi: 10.1016/0165-0270(94)90031-0. [DOI] [PubMed] [Google Scholar]
  2. Elzenga J. T., Keller C. P., Van Volkenburgh E. Patch clamping protoplasts from vascular plants : method for the quick isolation of protoplasts having a high success rate of gigaseal formation. Plant Physiol. 1991 Dec;97(4):1573–1575. doi: 10.1104/pp.97.4.1573. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Gradmann D., Klieber H. G., Hansen U. P. Reaction kinetic parameters for ion transport from steady-state current-voltage curves. Biophys J. 1987 Apr;51(4):569–585. doi: 10.1016/S0006-3495(87)83382-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
  5. Hansen U. P., Gradmann D., Sanders D., Slayman C. L. Interpretation of current-voltage relationships for "active" ion transport systems: I. Steady-state reaction-kinetic analysis of class-I mechanisms. J Membr Biol. 1981;63(3):165–190. doi: 10.1007/BF01870979. [DOI] [PubMed] [Google Scholar]
  6. Harrison S. M., Bers D. M. The effect of temperature and ionic strength on the apparent Ca-affinity of EGTA and the analogous Ca-chelators BAPTA and dibromo-BAPTA. Biochim Biophys Acta. 1987 Aug 13;925(2):133–143. doi: 10.1016/0304-4165(87)90102-4. [DOI] [PubMed] [Google Scholar]
  7. Klieber H. G., Gradmann D. Enzyme kinetics of the prime K+ channel in the tonoplast of Chara: selectivity and inhibition. J Membr Biol. 1993 Mar;132(3):253–265. doi: 10.1007/BF00235742. [DOI] [PubMed] [Google Scholar]
  8. Lew R. R., Serlin B. S., Schauf C. L., Stockton M. E. Red light regulates calcium-activated potassium channels in mougeotia plasma membrane. Plant Physiol. 1990 Mar;92(3):822–830. doi: 10.1104/pp.92.3.822. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Spalding E. P., Goldsmith MHM. Activation of K+ Channels in the Plasma Membrane of Arabidopsis by ATP Produced Photosynthetically. Plant Cell. 1993 Apr;5(4):477–484. doi: 10.1105/tpc.5.4.477. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Spalding E. P., Slayman C. L., Goldsmith M. H., Gradmann D., Bertl A. Ion channels in Arabidopsis plasma membrane : transport characteristics and involvement in light-induced voltage changes. Plant Physiol. 1992 May;99(1):96–102. doi: 10.1104/pp.99.1.96. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Thomine S., Zimmermann S., Guern J., Barbier-Brygoo H. ATP-Dependent Regulation of an Anion Channel at the Plasma Membrane of Protoplasts from Epidermal Cells of Arabidopsis Hypocotyls. Plant Cell. 1995 Dec;7(12):2091–2100. doi: 10.1105/tpc.7.12.2091. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Van Volkenburgh E., Cleland R. E. Light-stimulated cell expansion in bean (Phaseolus vulgaris L.) leaves. I. Growth can occur without photosynthesis. Planta. 1990 Aug;182(1):72–76. doi: 10.1007/BF00239986. [DOI] [PubMed] [Google Scholar]
  13. Van Volkenburgh E., Cleland R. E., Watanabe M. Light-stimulated cell expansion in bean (Phaseolus vulgaris L.) leaves. II. Quantity and quality of light required. Planta. 1990 Aug;182(1):77–80. doi: 10.1007/BF00239987. [DOI] [PubMed] [Google Scholar]

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

RESOURCES