Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1981 Dec;68(6):1494–1499. doi: 10.1104/pp.68.6.1494

Rapid Electric Responses of Oats to Phytochrome Show Membrane Processes Unrelated to Pelletability 1

Ian A Newman 1
PMCID: PMC426128  PMID: 16662133

Abstract

The electric potential difference changes observed on etiolated oat coleoptiles in response to phytochrome transformation have been further studied using contacts on the coleoptile surface. Results are given, at 0.4 second resolution, for the first 1.5 minutes after saturating flashes of light each lasting 1 second.

Responses to initial red (662 nanometers), to far red (about 700 nanometers and above) 10 minutes later, and to second red 10 minutes later still, all have time courses that are approximately Gaussian sigmoid in shape. The response to far red is of opposite sign to the response to red. Approximate magnitudes of the three changes, 1 minute after the light flash, are +6 millivolts for red, −10 millivolts for far red, +3.5 millivolts for the second red. It is argued that the observations reflect a hyperpolarization of the plasmalemma of coleoptile cells following red light and depolarization following far red. The response to red is not produced by a change in membrane permeability to K+. The mechanism could include a change to Na+ or Cl permeability or a modulation of an electrogenic pump: enhanced H+ extrusion, Ca2+ extrusion, or Cl uptake. The response to far red could be produced by the reverse of one of those changes.

The Gaussian curve is fitted to the data to determine the time at which the responses begin. Each response begins 4.5 seconds after the start of the flash of light. These delays are not related to the time course of phytochrome pelletability or redistribution in the cell. The delays may be due to some interaction of the transformed phytochrome with the plasma-lemma. Alternatively, the transformed phytochrome may interact quickly with some other structure which initiates a signal that takes 4.5 seconds to reach the plasmalemma.

Full text

PDF
1494

Selected References

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

  1. Brownlee C., Kendrick R. E. Ion Fluxes and Phytochrome Protons in Mung Bean Hypocotyl Segments: II. Fluxes of Chloride, Protons, and Orthophosphate in Apical and Subhook Segments. Plant Physiol. 1979 Aug;64(2):211–213. doi: 10.1104/pp.64.2.211. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Brownlee C., Kendrick R. E. Ion fluxes and phytochrome protons in mung bean hypocotyl segments: I. Fluxes of potassium. Plant Physiol. 1979 Aug;64(2):206–210. doi: 10.1104/pp.64.2.206. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Hale C. C., Roux S. J. Photoreversible calcium fluxes induced by phytochrome in oat coleoptile cells. Plant Physiol. 1980 Apr;65(4):658–662. doi: 10.1104/pp.65.4.658. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Jaffe M. J. Phytochrome-mediated bioelectric potentials in mung bean seedlings. Science. 1968 Nov 29;162(3857):1016–1017. doi: 10.1126/science.162.3857.1016. [DOI] [PubMed] [Google Scholar]
  5. Mackenzie J. M., Jr, Coleman R. A., Briggs W. R., Pratt L. H. Reversible redistribution of phytochrome within the cell upon conversion to its physiologically active form. Proc Natl Acad Sci U S A. 1975 Mar;72(3):799–803. doi: 10.1073/pnas.72.3.799. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Newman I. A., Briggs W. R. Phytochrome-mediated Electric Potential Changes in Oat Seedlings. Plant Physiol. 1972 Dec;50(6):687–693. doi: 10.1104/pp.50.6.687. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Pike C. S., Richardson A. E. Phytochrome-controlled Hydrogen Ion Excretion by Avena Coleoptiles. Plant Physiol. 1977 Apr;59(4):615–617. doi: 10.1104/pp.59.4.615. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Pratt L. H., Coleman R. A. Immunocytochemical localization of phytochrome. Proc Natl Acad Sci U S A. 1971 Oct;68(10):2431–2435. doi: 10.1073/pnas.68.10.2431. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Pratt L. H., Marmé D. Red Light-enhanced Phytochrome Pelletability: Re-examination and Further Characterization. Plant Physiol. 1976 Nov;58(5):686–692. doi: 10.1104/pp.58.5.686. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Pratt L. H. Phytochrome Pelletability Induced by Irradiation in Vivo: TEST FOR IN VITRO BINDING OF ADDED [S]PHYTOCHROME. Plant Physiol. 1980 Nov;66(5):903–907. doi: 10.1104/pp.66.5.903. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Quail P. H., Briggs W. R. Irradiation-enhanced Phytochrome Pelletability: Requirement for Phosphorylative Energy in Vivo. Plant Physiol. 1978 Nov;62(5):773–778. doi: 10.1104/pp.62.5.773. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Quail P. H., Briggs W. R. Phytochrome Pelletability Induced by Irradiation in Vivo: MIXING EXPERIMENTS. Plant Physiol. 1980 Nov;66(5):908–910. doi: 10.1104/pp.66.5.908. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Roux S. J., Yguerabide J. Photoreversible conductance changes induced by phytochrome in model lipid membranes. Proc Natl Acad Sci U S A. 1973 Mar;70(3):762–764. doi: 10.1073/pnas.70.3.762. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Tanada T. A rapid photoreversible response of barley root tips in the presence of 3-indoleacetic Acid. Proc Natl Acad Sci U S A. 1968 Feb;59(2):376–380. doi: 10.1073/pnas.59.2.376. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES