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. 1994 Sep;106(1):329–336. doi: 10.1104/pp.106.1.329

Response of Fructan to Water Deficit in Growing Leaves of Tall Fescue.

W G Spollen 1, C J Nelson 1
PMCID: PMC159531  PMID: 12232332

Abstract

Changes in dry matter and water-soluble carbohydrate components, especially fructan, were examined in the basal 25 mm of expanding leaf blades of tall fescue (Festuca arundinacea Schreb.) to assess their roles in plant response to water deficit. Water was withheld from vegetative plants grown in soil in controlled-environment chambers. As stress progressed, leaf elongation rate decreased sooner in the light period than it did in the dark period. The decrease in growth rate in the dark period was associated with a decrease in local relative elongation rates and a shortening of the elongation zone from about 25 mm (control) to 15 mm. Dry matter content of the leaf base increased 23% during stress, due mainly to increased water-soluble carbohydrate near the ligule and to increased water-soluble, carbohydrate-free dry matter at distal positions. Sucrose content increased 258% in the leaf base, but especially (over 4-fold) within 10 mm of the ligule. Hexose content increased 187% in the leaf base. Content of total fructan decreased to 69% of control, mostly in regions farther from the ligule. Fructan hydrolysis could account for the hexose accumulated. Stress caused the osmotic potential to decrease throughout the leaf base, but more toward the ligule. With stress there was 70% less direct contribution of low-degree-of-polymerization fructan to osmotic potential in the leaf base, but that for sucrose and hexose increased 96 and 67%, respectively. Thus, fructan metabolism is involved but fructan itself contributes only indirectly to osmotic adjustment.

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Selected References

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

  1. Allard G., Nelson C. J. Photosynthate partitioning in Basal zones of tall fescue leaf blades. Plant Physiol. 1991 Mar;95(3):663–668. doi: 10.1104/pp.95.3.663. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bieleski R. L. Fructan Hydrolysis Drives Petal Expansion in the Ephemeral Daylily Flower. Plant Physiol. 1993 Sep;103(1):213–219. doi: 10.1104/pp.103.1.213. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Gastal F., Nelson C. J. Nitrogen Use within the Growing Leaf Blade of Tall Fescue. Plant Physiol. 1994 May;105(1):191–197. doi: 10.1104/pp.105.1.191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Matsuda K., Riazi A. Stress-induced osmotic adjustment in growing regions of barley leaves. Plant Physiol. 1981 Sep;68(3):571–576. doi: 10.1104/pp.68.3.571. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Michelena V. A., Boyer J. S. Complete turgor maintenance at low water potentials in the elongating region of maize leaves. Plant Physiol. 1982 May;69(5):1145–1149. doi: 10.1104/pp.69.5.1145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Schnyder H., Nelson C. J., Coutts J. H. Assessment of spatial distribution of growth in the elongation zone of grass leaf blades. Plant Physiol. 1987 Sep;85(1):290–293. doi: 10.1104/pp.85.1.290. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Schnyder H., Nelson C. J. Growth rates and assimilate partitioning in the elongation zone of tall fescue leaf blades at high and low irradiance. Plant Physiol. 1989 Jul;90(3):1201–1206. doi: 10.1104/pp.90.3.1201. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Schnyder H., Nelson C. J., Spollen W. G. Diurnal Growth of Tall Fescue Leaf Blades : II. Dry Matter Partitioning and Carbohydrate Metabolism in the Elongation Zone and Adjacent Expanded Tissue. Plant Physiol. 1988 Apr;86(4):1077–1083. doi: 10.1104/pp.86.4.1077. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Spollen W. G., Nelson C. J. Characterization of fructan from mature leaf blades and elongation zones of developing leaf blades of wheat, tall fescue, and timothy. Plant Physiol. 1988 Dec;88(4):1349–1353. doi: 10.1104/pp.88.4.1349. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Volenec J. J., Nelson C. J. Carbohydrate metabolism in leaf meristems of tall fescue : I. Relationship to genetically altered leaf elongation rates. Plant Physiol. 1984 Mar;74(3):590–594. doi: 10.1104/pp.74.3.590. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Wagner W., Wiemken A. Enzymology of Fructan Synthesis in Grasses: Properties of Sucrose-Sucrose-Fructosyltransferase in Barley Leaves (Hordeum vulgare L. cv Gerbel). Plant Physiol. 1987 Nov;85(3):706–710. doi: 10.1104/pp.85.3.706. [DOI] [PMC free article] [PubMed] [Google Scholar]

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