Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1985 Mar;77(3):524–531. doi: 10.1104/pp.77.3.524

Sugar Efflux from Maize (Zea mays L.) Pedicel Tissue 1

Gregory A Porter 1,2, Daniel P Knievel 1,2, Jack C Shannon 1,2
PMCID: PMC1064557  PMID: 16664091

Abstract

Sugar release from the pedicel tissue of maize (Zea mays L.) kernels was studied by removing the distal portion of the kernel and the lower endosperm, followed by replacement of the endosperm with an agar solute trap. Sugars were unloaded into the apoplast of the pedicel and accumulated in the agar trap while the ear remained attached to the maize plant. The kinetics of 14C-assimilate movement into treated versus intact kernels were comparable. The rate of unloading declined with time, but sugar efflux from the pedicel continued for at least 6 hours and in most experiments the unloading rates approximated those necessary to support normal kernel growth rates. The unloading process was challenged with a variety of buffers, inhibitors, and solutes in order to characterize sugar unloading from this tissue.

Unloading was not affected by apoplastic pH or a variety of metabolic inhibitors. Although p-chloromercuribenzene sulfonic acid (PCMBS), a nonpenetrating sulfhydryl group reagent, did not affect sugar unloading, it effectively inhibited extracellular acid invertase. When the pedicel cups were pretreated with PCMBS, at least 60% of sugars unloaded from the pedicel could be identified as sucrose. Unloading was inhibited up to 70% by 10 millimolar CaCl2. Unloading was stimulated by 15 millimolar ethyleneglycol-bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid which partially reversed the inhibitory effects of Ca2+. Based on these results, we suggest that passive efflux of sucrose occurs from the maize pedicel symplast followed by extracellular hydrolysis to hexoses.

Full text

PDF
524

Images in this article

Selected References

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

  1. Anderson J. M. Release of Sucrose from Vicia faba L. Leaf Discs. Plant Physiol. 1983 Feb;71(2):333–340. doi: 10.1104/pp.71.2.333. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Felker F. C., Shannon J. C. Movement of C-labeled Assimilates into Kernels of Zea mays L: III. AN ANATOMICAL EXAMINATION AND MICROAUTORADIOGRAPHIC STUDY OF ASSIMILATE TRANSFER. Plant Physiol. 1980 May;65(5):864–870. doi: 10.1104/pp.65.5.864. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Fellows R. J., Egli D. B., Leggett J. E. A Pod Leakage Technique for Phloem Translocation Studies in Soybean (Glycine max [L.] Merr.). Plant Physiol. 1978 Nov;62(5):812–814. doi: 10.1104/pp.62.5.812. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Giaquinta R. T., Lin W., Sadler N. L., Franceschi V. R. Pathway of Phloem unloading of sucrose in corn roots. Plant Physiol. 1983 Jun;72(2):362–367. doi: 10.1104/pp.72.2.362. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Giaquinta R. Evidence for Phloem loading from the apoplast: chemical modification of membrane sulfhydryl groups. Plant Physiol. 1976 Jun;57(6):872–875. doi: 10.1104/pp.57.6.872. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Giaquinta R. Phloem Loading of Sucrose: pH Dependence and Selectivity. Plant Physiol. 1977 Apr;59(4):750–755. doi: 10.1104/pp.59.4.750. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Giaquinta R. Sucrose Hydrolysis in Relation to Phloem Translocation in Beta vulgaris. Plant Physiol. 1977 Sep;60(3):339–343. doi: 10.1104/pp.60.3.339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Huber S. C., Moreland D. E. Co-transport of Potassium and Sugars across the Plasmalemma of Mesophyll Protoplasts. Plant Physiol. 1981 Jan;67(1):163–169. doi: 10.1104/pp.67.1.163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. King R. W., Zeevaart J. A. Enhancement of Phloem exudation from cut petioles by chelating agents. Plant Physiol. 1974 Jan;53(1):96–103. doi: 10.1104/pp.53.1.96. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Rehfeld D. W., Jensen R. G. Metabolism of Separated Leaf Cells: III. Effects of Calcium and Ammonium on Product Distribution During Photosynthesis with Cotton Cells. Plant Physiol. 1973 Jul;52(1):17–22. doi: 10.1104/pp.52.1.17. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Shannon J. C. Carbon-14 Distribution in Carbohydrates of Immature Zea mays. Kernels Following CO(2) Treatment of Intact Plants. Plant Physiol. 1968 Aug;43(8):1215–1220. doi: 10.1104/pp.43.8.1215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Shannon J. C. Movement of C-Labeled Assimilates into Kernels of Zea mays L: I. Pattern and Rate of Sugar Movement. Plant Physiol. 1972 Feb;49(2):198–202. doi: 10.1104/pp.49.2.198. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Shannon J. C. Movement of C-Labeled Assimilates into Kernels of Zea mays L: II. Invertase Activity of the Pedicel and Placento-Chalazal Tissues. Plant Physiol. 1972 Feb;49(2):203–206. doi: 10.1104/pp.49.2.203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Thorne J. H. Morphology and ultrastructure of maternal seed tissues of soybean in relation to the import of photosynthate. Plant Physiol. 1981 May;67(5):1016–1025. doi: 10.1104/pp.67.5.1016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Thorne J. H., Rainbird R. M. An in vivo technique for the study of Phloem unloading in seed coats of developing soybean seeds. Plant Physiol. 1983 May;72(1):268–271. doi: 10.1104/pp.72.1.268. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES