Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1995 Oct;109(2):579–585. doi: 10.1104/pp.109.2.579

Sucrose Release into the Endosperm Cavity of Wheat Grains Apparently Occurs by Facilitated Diffusion across the Nucellar Cell Membranes.

N Wang 1, D B Fisher 1
PMCID: PMC157623  PMID: 12228614

Abstract

Nutrients required for the growth of the embryo and endosperm of developing wheat (Triticum aestivum L.) grains are released into the endosperm cavity from the maternal tissues across the nucellar cell plasma membranes. We followed the uptake and efflux of sugars into and out of the nucellus by slicing grains longitudinally through the endosperm cavity to expose the nucellar surface to experimental solutions. Sucrose uptake and efflux are passive processes. Neither was sensitive to metabolic inhibitors, pH, or potassium concentration. p-Chloromercuribenzene sulfonate, however, strongly inhibited both uptake and efflux, although not equally. Except for p-chloromercuribenzene sensitivity, these characteristics of efflux and the insensitivity of Suc movement to turgor pressure are similar to those of sucrose release from maize pedicels, but they contrast with legume seed coats. Although the evidence is incomplete, movement appears to be carrier mediated rather than channel mediated. In vitro rates of sucrose efflux were similar to or somewhat less than in vivo rates, suggesting that transport across the nucellar cell membranes could be a factor in the control of assimilate import into the grain.

Full Text

The Full Text of this article is available as a PDF (725.7 KB).

Selected References

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

  1. Ellis E. C., Turgeon R., Spanswick R. M. Quantitative Analysis of Photosynthate Unloading in Developing Seeds of Phaseolus vulgaris L. : II. Pathway and Turgor Sensitivity. Plant Physiol. 1992 Jun;99(2):643–651. doi: 10.1104/pp.99.2.643. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Fisher D. B., Wang N. A Kinetic and Microautoradiographic Analysis of [14C]Sucrose Import by Developing Wheat Grains. Plant Physiol. 1993 Feb;101(2):391–398. doi: 10.1104/pp.101.2.391. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Fisher D. B., Wang N. Sucrose Concentration Gradients along the Post-Phloem Transport Pathway in the Maternal Tissues of Developing Wheat Grains. Plant Physiol. 1995 Oct;109(2):587–592. doi: 10.1104/pp.109.2.587. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Nikaido H., Rosenberg E. Y. Effect on solute size on diffusion rates through the transmembrane pores of the outer membrane of Escherichia coli. J Gen Physiol. 1981 Feb;77(2):121–135. doi: 10.1085/jgp.77.2.121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Porter G. A., Knievel D. P., Shannon J. C. Assimilate Unloading from Maize (Zea mays L.) Pedicel Tissues : II. Effects of Chemical Agents on Sugar, Amino Acid, and C-Assimilate Unloading. Plant Physiol. 1987 Oct;85(2):558–565. doi: 10.1104/pp.85.2.558. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. SCHULTZ S. G., SOLOMON A. K. Determination of the effective hydrodynamic radii of small molecules by viscometry. J Gen Physiol. 1961 Jul;44:1189–1199. doi: 10.1085/jgp.44.6.1189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Wang N., Fisher D. B. Monitoring Phloem Unloading and Post-Phloem Transport by Microperfusion of Attached Wheat Grains. Plant Physiol. 1994 Jan;104(1):7–16. doi: 10.1104/pp.104.1.7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Wang N., Fisher D. B. The Use of Fluorescent Tracers to Characterize the Post-Phloem Transport Pathway in Maternal Tissues of Developing Wheat Grains. Plant Physiol. 1994 Jan;104(1):17–27. doi: 10.1104/pp.104.1.17. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES