Abstract
The chromometallic dye murexide was used to measure photoreversible Ca fluxes in apical tips of etiolated oat coleoptiles and in suspension cultures of protoplasts derived from the coleoptile segments. Phytochrome presence in the protoplasts was indicated by a repeatably photoreversible ΔA(725 - 800 nm) of >0.001 A centimeters−1, recorded on a dual wavelength spectrophotometer. Concentrations of Ca in the solution bathing the cells were observed to change photoreversibly, red irradiation inducing an increase in the medium Ca concentration and subsequent farred irradiation inducing a decrease down to near dark control levels. These changes could be measured in media with or without exogenously added Ca. Protoplasts from green primary leaves of oat, which had no spectro-photometrically detectable phytochrome, showed no photoreversible Ca fluxes when measured by the same method. These data imply that red light induces an efflux of Ca from phytochrome-containing cells and that far red light can reverse this change by promoting a Ca reentry into these cells.
Full text
PDF




Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Briggs W. R., Chon H. P. The physiological versus the spectrophotometric status of phytochrome in corn coleoptiles. Plant Physiol. 1966 Sep;41(7):1159–1166. doi: 10.1104/pp.41.7.1159. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Briggs W. R., Siegelman H. W. Distribution of Phytochrome in Etiolated Seedlings. Plant Physiol. 1965 Sep;40(5):934–941. doi: 10.1104/pp.40.5.934. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Georgevich G., Cedel T. E., Roux S. J. Use of I-labeled phytochrome to quantitate phytochrome binding to membranes of Avena sativa. Proc Natl Acad Sci U S A. 1977 Oct;74(10):4439–4443. doi: 10.1073/pnas.74.10.4439. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- McArthur J. A. Effect of red light on geotropism in pea epicotyls. Plant Physiol. 1979 Jan;63(1):218–220. doi: 10.1104/pp.63.1.218. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mettler I. J., Leonard R. T. Ion transport in isolated protoplasts from tobacco suspension cells: I. General characteristics. Plant Physiol. 1979 Jan;63(1):183–190. doi: 10.1104/pp.63.1.183. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ohnishi S. T. Characterization of the murexide method: dual-wavelength spectrophotometry of cations under physiological conditions. Anal Biochem. 1978 Mar;85(1):165–179. doi: 10.1016/0003-2697(78)90287-7. [DOI] [PubMed] [Google Scholar]
- Pike C. S., Richardson A. E. Red light and auxin effects on rubidium uptake by oat coleoptile and pea epicotyl segments. Plant Physiol. 1979 Jan;63(1):139–141. doi: 10.1104/pp.63.1.139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Scarpa A. Spectrophotometric measurement of calcium by murexide. Methods Enzymol. 1972;24:343–351. doi: 10.1016/0076-6879(72)24082-4. [DOI] [PubMed] [Google Scholar]
- Tepfer M., Cleland R. E. A Comparison of Acid-induced Cell Wall Loosening in Valonia ventricosa and in Oat Coleoptiles. Plant Physiol. 1979 May;63(5):898–902. doi: 10.1104/pp.63.5.898. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wilkins M. B. Red Light and the Geotropic Response of the Avena Coleoptile. Plant Physiol. 1965 Jan;40(1):24–34. doi: 10.1104/pp.40.1.24. [DOI] [PMC free article] [PubMed] [Google Scholar]
