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Modification of chemical properties of cell wall polysaccharides in the inner tissues by white light in relation to the decrease in tissue tension in Pisum sativum epicotyls
Author(s) -
Miyamoto Kensuke,
Mitani Yuko,
Soga Kouichi,
Ueda Junichi,
Wakabayashi Kazuyuki,
Hoson Takayuki,
Kamisaka Seiichiro,
Masuda Yoshio
Publication year - 1997
Publication title -
physiologia plantarum
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.351
H-Index - 146
eISSN - 1399-3054
pISSN - 0031-9317
DOI - 10.1111/j.1399-3054.1997.tb01817.x
Subject(s) - xyloglucan , cell wall , pisum , polysaccharide , biophysics , sativum , pectin , chemistry , biochemistry , biology , botany
When white light irradiation inhibits shoot growth in derooted pea ( Pisum sativum L. cv. Alaska) cuttings, it decreases tissue tension, a driving force for shoot growth, by making the cell wall of the inner tissues mechanically rigid. To elucidate the mechanism by which light affects the mechanical properties of the cell wall in the inner tissues, its effect on the chemical properties of the cell walls was studied by analyzing qualitatively and quantitatively cell wall polysaccharides in the epdidermis and inner tissue of pea epicotyls grown in both dark and light. The amount of polysaccharides per subhook in the cell walls of both tissues increased during a 4‐h dark incubation. Light suppressed the increase in hemicellulosic (HC)‐II and cellulosic polysaccharides in the inner tissues, while it did not affect the increase in other wall fractions in either the epidermal or subepidermal tissues. No light effect was observed on the neutral sugar compositions of pectin, HC‐I or HC‐II fractions in either of the tissues. Light increased the mass‐average molecular mass of xyloglucan and rhamnoarabinogalactan in HC‐II fractions in the inner tissues, while such an effect was not observed in the epidermis. These facts suggest that the light‐induced decrease in the tissue tension in pea epicotyls is caused by an increase in the molecular size of xyloglucan, rhamnoarabinogalactan in the HC‐II fraction and/or the suppression of the synthesis of HC‐II and cellulosic polysaccharides in the inner tissues.