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. 1992 Jan;98(1):369–379. doi: 10.1104/pp.98.1.369

Changes in Molecular Size of Previously Deposited and Newly Synthesized Pea Cell Wall Matrix Polysaccharides 1

Effects of Auxin and Turgor

Lawrence D Talbott 1,2, Peter M Ray 1
PMCID: PMC1080192  PMID: 16668638

Abstract

Effects of indoleacetic acid (IAA) and of turgor changes on the apparent molecular mass (Mr) distributions of cell wall matrix polysaccharides from etiolated pea (Pisum sativum L.) epicotyl segments were determined by gel filtration chromatography. IAA causes a two- to threefold decline in the peak Mr of xyloglucan, relative to minus-auxin controls, to occur within 0.5 hour. IAA causes an even larger decrease in the peak Mr concurrently biosynthesized xyloglucan, as determined by [3H]fucose labeling, but this effect begins only after 1 hour. In contrast, IAA does not appreciably affect the Mr distributions of pectic polyuronides or hemicellulosic arabinose/galactose polysaccharides within 1.5 hours. However, after epicotyl segments are cut, their peak polyuronide Mr increases and later decreases, possibly as part of a wound response. Xyloglucan also undergoes IAA-independent changes in its Mr distribution after cutting segments. In addition, the peak Mr of newly deposited xyloglucan increases from about 9 kilodaltons shortly after deposition to about 30 kilodaltons within 0.5 hour. This may represent a process of integration into the cell wall. A step increase in turgor causes the peak Mr of previously deposited xyloglucan (but not of the other major polymers) to increase about 10-fold within 0.5 hour, returning to its initial value by 1.5 hours. This upshift may comprise a feedback mechanism that decreases wall extensibility when the rate of wall extension suddenly increases. IAA-induced reduction of xyloglucan Mr might cause wall loosening that leads to cell enlargement, as has been suggested previously, but the lack of a simple relation between xyloglucan Mr and elongation rate indicates that loosening must also involve other wall factors, one of which might be the deposition of new xyloglucan of much smaller size. Although the Mr shifts in polyuronides may represent changes in noncovalent association, and for xyloglucan this cannot be completely excluded, xyloglucan seems to participate in a dynamic process that can both decrease and increase its chain length, possible mechanisms for which are suggested.

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Selected References

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

  1. Abdul-Baki A. A., Ray P. M. Regulation by auxin of carbohydrate metabolism involved in cell wall synthesis by pea stem tissue. Plant Physiol. 1971 Apr;47(4):537–544. doi: 10.1104/pp.47.4.537. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Albersheim P. The walls of growing plant cells. Sci Am. 1975 Apr;232(4):80–95. doi: 10.1038/scientificamerican0475-80. [DOI] [PubMed] [Google Scholar]
  3. Barkley G. M., Evans M. L. Timing of the auxin response in etiolated pea stem sections. Plant Physiol. 1970 Feb;45(2):143–147. doi: 10.1104/pp.45.2.143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Byrne H., Christou N. V., Verma D. P., Maclachlan G. A. Purification and characterization of two cellulases from auxin-treated pea epicotyls. J Biol Chem. 1975 Feb 10;250(3):1012–1018. [PubMed] [Google Scholar]
  5. Camirand A., Maclachlan G. Biosynthesis of the fucose-containing xyloglucan nonasaccharide by pea microsomal membranes. Plant Physiol. 1986 Oct;82(2):379–383. doi: 10.1104/pp.82.2.379. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Cosgrove D. J. Cell wall yield properties of growing tissue : evaluation by in vivo stress relaxation. Plant Physiol. 1985 Jun;78(2):347–356. doi: 10.1104/pp.78.2.347. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cosgrove D. J., Van Volkenburgh E., Cleland R. E. Stress relaxation of cell walls and the yield threshold for growth: demonstration and measurement by micro-pressure probe and psychrometer techniques. Planta. 1984;162(1):46–54. doi: 10.1007/BF00397420. [DOI] [PubMed] [Google Scholar]
  8. Elorza V., Mormeneo S., Garcia de la Cruz F., Gimeno C., Sentandreu R. Evidence for the formation of covalent bonds between macromolecules in the domain of the wall of Candida albicans mycelial cells. Biochem Biophys Res Commun. 1989 Aug 15;162(3):1118–1125. doi: 10.1016/0006-291x(89)90789-4. [DOI] [PubMed] [Google Scholar]
  9. Green P. B., Cummins W. R. Growth rate and turgor pressure: auxin effect studies with an automated apparatus for single coleoptiles. Plant Physiol. 1974 Dec;54(6):863–869. doi: 10.1104/pp.54.6.863. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hayashi T., Wong Y. S., Maclachlan G. Pea Xyloglucan and Cellulose : II. Hydrolysis by Pea Endo-1,4-beta-Glucanases. Plant Physiol. 1984 Jul;75(3):605–610. doi: 10.1104/pp.75.3.605. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Hohl M., Hong Y. N., Schopfer P. Acid- and Enzyme-Mediated Solubilization of Cell-Wall beta-1.3,beta-1.4-d-Glucan in Maize Coleoptiles : Implications for Auxin-Mediated Growth. Plant Physiol. 1991 Apr;95(4):1012–1018. doi: 10.1104/pp.95.4.1012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hoson T., Nevins D. J. beta-d-Glucan Antibodies Inhibit Auxin-Induced Cell Elongation and Changes in the Cell Wall of Zea Coleoptile Segments. Plant Physiol. 1989 Aug;90(4):1353–1358. doi: 10.1104/pp.90.4.1353. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Inouhe M., Nevins D. J. Inhibition of auxin-induced cell elongation of maize coleoptiles by antibodies specific for cell wall glucanases. Plant Physiol. 1991 Jun;96(2):426–431. doi: 10.1104/pp.96.2.426. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Jacobs M., Ray P. M. Promotion of Xyloglucan Metabolism by Acid pH. Plant Physiol. 1975 Sep;56(3):373–376. doi: 10.1104/pp.56.3.373. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Jacobs M., Ray P. M. Rapid Auxin-induced Decrease in Free Space pH and Its Relationship to Auxin-induced Growth in Maize and Pea. Plant Physiol. 1976 Aug;58(2):203–209. doi: 10.1104/pp.58.2.203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Kutschera U., Briggs W. R. Rapid auxin-induced stimulation of cell wall synthesis in pea internodes. Proc Natl Acad Sci U S A. 1987 May;84(9):2747–2751. doi: 10.1073/pnas.84.9.2747. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Labavitch J. M., Ray P. M. Relationship between Promotion of Xyloglucan Metabolism and Induction of Elongation by Indoleacetic Acid. Plant Physiol. 1974 Oct;54(4):499–502. doi: 10.1104/pp.54.4.499. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Labavitch J. M., Ray P. M. Turnover of cell wall polysaccharides in elongating pea stem segments. Plant Physiol. 1974 May;53(5):669–673. doi: 10.1104/pp.53.5.669. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Loescher W. H., Nevins D. J. Turgor-dependent Changes in Avena Coleoptile Cell Wall Composition. Plant Physiol. 1973 Sep;52(3):248–251. doi: 10.1104/pp.52.3.248. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Loescher W., Nevins D. J. Auxin-induced Changes in Avena Coleoptile Cell Wall Composition. Plant Physiol. 1972 Nov;50(5):556–563. doi: 10.1104/pp.50.5.556. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. McDougall G. J., Fry S. C. Xyloglucan oligosaccharides promote growth and activate cellulase: evidence for a role of cellulase in cell expansion. Plant Physiol. 1990 Jul;93(3):1042–1048. doi: 10.1104/pp.93.3.1042. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Ordin L. Effect of Water Stress on Cell Wall Metabolism of Avena Coleoptile Tissue. Plant Physiol. 1960 Jul;35(4):443–450. doi: 10.1104/pp.35.4.443. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Ray P. M. Radioautographic study of cell wall deposition in growing plant cells. J Cell Biol. 1967 Dec;35(3):659–674. doi: 10.1083/jcb.35.3.659. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Ray P. M. Regulation of beta-Glucan Synthetase Activity by Auxin in Pea Stem Tissue: I. Kinetic Aspects. Plant Physiol. 1973 Apr;51(4):601–608. doi: 10.1104/pp.51.4.601. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Talbott L. D., Ray P. M. Molecular size and separability features of pea cell wall polysaccharides : implications for models of primary wall structure. Plant Physiol. 1992 Jan;98(1):357–368. doi: 10.1104/pp.98.1.357. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Terry M. E., Jones R. L. Soluble Cell Wall Polysaccharides Released from Pea Stems by Centrifugation : I. EFFECT OF AUXIN. Plant Physiol. 1981 Sep;68(3):531–537. doi: 10.1104/pp.68.3.531. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Verma D. P., Maclachlan G. A., Byrne H., Ewings D. Regulation and in vitro translation of messenger ribonucleic acid for cellulase from auxin-treated pea epicotyls. J Biol Chem. 1975 Feb 10;250(3):1019–1026. [PubMed] [Google Scholar]
  28. Wakabayashi K., Sakurai N., Kuraishi S. Differential Effect of Auxin on Molecular Weight Distributions of Xyloglucans in Cell Walls of Outer and Inner Tissues from Segments of Dark Grown Squash (Cucurbita maxima Duch.) Hypocotyls. Plant Physiol. 1991 Apr;95(4):1070–1076. doi: 10.1104/pp.95.4.1070. [DOI] [PMC free article] [PubMed] [Google Scholar]

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