首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Role of xyloglucan breakdown in epidermal cell walls for auxininduced elongation of azuki bean epicotyl segments
Authors:Takayuki Hoson  Yoshiaki Sone  Akira Misaki  Yoshio Masuda
Institution:Dept of Biology, Faculty of Science, Osaka City Univ., Sumiyoshi-ku, Osaka 558, Japan;Dept of Food and Nutrition, Faculty of Science of Living, Osaka City Univ., Sumiyoshi-ku, Osaka 558, Japan;Laboratory of Biology, Tezukayama College, Nara 631, Japan.
Abstract:Auxin-induced elongation of epicotyl segments of azuki bean ( Vigna angularis Ohwi et Ohashi cv. Takara) was suppressed by a fucose-binding lectin from Tetragonolobus purpureas Moench and by polyclonal antibodies raised against xyloglucan heptasaccharide (Xyl3Glc4) when the cuticle present in the outer surface of epicotyls was abraded. In contrast, elongation of non-abraded segments was not influenced by the lectin or the antibodies. Epicotyl segments, from which the epidermal and the outer cortical cells had been removed, elongated rapidly for 2 h and than only slowly. Auxin slightly stimulated elongation of the inner tissue segments in the phase of slow growth. Neither in the presence nor in the absence of auxin did the lectin or the antibodies affect elongation of the inner tissue segments. The split portions of outer surface-abraded epicotyl segments incubated in buffer extended outward, and auxininhibited this outward bending. The lectin and the antibodies reversed the effect of auxin on bending. The fucose-binding lectin pretreated with fucose or the immunoglobulin fraction obtained from preimmune serum exhibited little or no inhibitory effect on auxin-induced elongation of abraded or split segments. These results support the view that a breakdown of xyloglucans in the epidermal cell walls plays an essential role in auxin-induced elongation in dicotyledons.
Keywords:Antibody  auxin  azuki bean  cell wall  epicotyl  epidermis  fucose  growth regulation  lectin              Vigna angularis            xyloglucan
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号