Noriaki Munekata1, Taku Tsuyama2, Ichiro Kamei1, Yoshio Kijidani1, Keiji Takabe3. 1. Faculty of Agriculture, University of Miyazaki, Miyazaki, 889-2192, Japan. 2. Faculty of Agriculture, University of Miyazaki, Miyazaki, 889-2192, Japan. tsuyama@cc.miyazaki-u.ac.jp. 3. Graduate School of Agriculture, Kyoto University, Kyoto, 606-8502, Japan.
Abstract
MAIN CONCLUSION: The feruloylarabinoxylan deposition was initiated at the formation of the secondary cell wall, especially S2 layer in moso bamboo, which may affect crosslinking between cell wall components and plant growth. Hemicelluloses, major components of plant cell walls that are hydrogen bonded to cellulose and covalently bound to lignin, are crucial determinants of cell wall properties. Especially in commelinid monocotyledons, arabinoxylan is often esterified with ferulic acid, which is essential to crosslinking with cell wall components. However, the deposition patterns and localization of ferulic acid during cell wall formation remain unclear. In this study, developing moso bamboo (Phyllostachys pubescens) culms were used to elucidate deposition patterns of hemicelluloses including feruloylarabinoxylan. Ferulic acid content peaked with cessation of elongation growth, and thereafter decreased and remained stable as culm development proceeded. During primary cell wall (PCW) formation, xyloglucan and (1,3;1,4)-β-glucan signals were detected in all tissues. Along with culm development, arabinoxylan and feruloylarabinoxylan signals were sequentially observed in the protoxylem, vascular fibers and metaxylem, and parenchyma. Feruloylarabinoxylan signals were observed slightly later than arabinoxylan signals. Arabinoxylan signals were observed throughout the compound middle lamella and secondary cell wall (SCW), whereas the feruloylarabinoxylan signal was localized to the S2 layer of the SCW. These results indicate that the biosynthesis of hemicelluloses is regulated in accordance with cell wall layers. Feruloylarabinoxylan deposition may be initiated at the formation of SCW, especially S2 layer formation. Ferulic acid-mediated linkages of arabinoxylan-arabinoxylan and arabinoxylan-lignin would arise during SCW formation with the cessation of elongation growth.
MAIN CONCLUSION: The feruloylarabinoxylan deposition was initiated at the formation of the secondary cell wall, especially S2 layer in moso bamboo, which may affect crosslinking between cell wall components and plant growth. Hemicelluloses, major components of plant cell walls that are hydrogen bonded to cellulose and covalently bound to lignin, are crucial determinants of cell wall properties. Especially in commelinid monocotyledons, arabinoxylan is often esterified with ferulic acid, which is essential to crosslinking with cell wall components. However, the deposition patterns and localization of ferulic acid during cell wall formation remain unclear. In this study, developing moso bamboo (Phyllostachys pubescens) culms were used to elucidate deposition patterns of hemicelluloses including feruloylarabinoxylan. Ferulic acid content peaked with cessation of elongation growth, and thereafter decreased and remained stable as culm development proceeded. During primary cell wall (PCW) formation, xyloglucan and (1,3;1,4)-β-glucan signals were detected in all tissues. Along with culm development, arabinoxylan and feruloylarabinoxylan signals were sequentially observed in the protoxylem, vascular fibers and metaxylem, and parenchyma. Feruloylarabinoxylan signals were observed slightly later than arabinoxylan signals. Arabinoxylan signals were observed throughout the compound middle lamella and secondary cell wall (SCW), whereas the feruloylarabinoxylan signal was localized to the S2 layer of the SCW. These results indicate that the biosynthesis of hemicelluloses is regulated in accordance with cell wall layers. Feruloylarabinoxylan deposition may be initiated at the formation of SCW, especially S2 layer formation. Ferulic acid-mediated linkages of arabinoxylan-arabinoxylan and arabinoxylan-lignin would arise during SCW formation with the cessation of elongation growth.
Authors: Laura E Bartley; Matthew L Peck; Sung-Ryul Kim; Berit Ebert; Chithra Manisseri; Dawn M Chiniquy; Robert Sykes; Lingfang Gao; Carsten Rautengarten; Miguel E Vega-Sánchez; Peter I Benke; Patrick E Canlas; Peijian Cao; Susan Brewer; Fan Lin; Whitney L Smith; Xiaohan Zhang; Jay D Keasling; Rolf E Jentoff; Steven B Foster; Jizhong Zhou; Angela Ziebell; Gynheung An; Henrik V Scheller; Pamela C Ronald Journal: Plant Physiol Date: 2013-02-07 Impact factor: 8.340
Authors: Wagner R de Souza; Polyana K Martins; Jackie Freeman; Till K Pellny; Louise V Michaelson; Bruno L Sampaio; Felipe Vinecky; Ana P Ribeiro; Barbara A D B da Cunha; Adilson K Kobayashi; Patricia A de Oliveira; Raquel B Campanha; Thályta F Pacheco; Danielly C I Martarello; Rogério Marchiosi; Osvaldo Ferrarese-Filho; Wanderley D Dos Santos; Robson Tramontina; Fabio M Squina; Danilo C Centeno; Marília Gaspar; Marcia R Braga; Marco A S Tiné; John Ralph; Rowan A C Mitchell; Hugo B C Molinari Journal: New Phytol Date: 2018-01-08 Impact factor: 10.151