Solid-state 13C NMR spectroscopy studies of xylans in the cell wall of Palmaria palmata (L. Kuntze, Rhodophyta)

被引:54
|
作者
Lahaye, M
Rondeau-Mouro, C
Deniaud, E
Buléon, A
机构
[1] INRA, Unite Rech Polysaccharides, F-44316 Nantes, France
[2] INRA, Unite Phys Chim Macromol, Ctr Rech Nantes, F-44316 Nantes, France
[3] IFREMER, Lab Biochim Prot & Qualite, F-44311 Nantes, France
关键词
Palmaria palmata; Rhodophyta; xylan; solid-state NMR; cell wall;
D O I
10.1016/S0008-6215(03)00241-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The chemical structure and interactions of the cell wall polysaccharides from the red edible seaweed Palmaria palmata were studied by liquid-like magic-angle-spinning (MAS) and cross-polarization MAS (CPMAS) solid-state C-13 NMR spectroscopy. The liquid-like MAS and CPMAS C-13 NMR spectra of the rehydrated algal powder revealed the presence of beta-(1-->4)/beta-(1-->3)-linked D-xylan with chemical shifts close to those observed in the solution C-13 NMR spectrum of the polysaccharide. Observation of mix-linked xylan in the liquid-like MAS C-13 NMR spectrum indicated that part of this cell wall polysaccharide is loosely held in the alga. The CPMAS NMR spectrum of the dry algal powder alcohol insoluble residue (AIR) showed broad peaks most of which corresponded to the mix-linked xylan. Hydration of AIR induced a marked increase in the signal resolution also in the CPMAS NMR spectra together with a shift of the C-3 and C-4 signals of the (1-->3)- and (1-->4)-linked xylose, respectively. Such modifications were present in the spectrum of hydrated (1-->3)-linked xylan from the green seaweed Caulerpa taxifolia and absent in that of (1-->4)-linked xylan from P. palmata. This result emphasizes the important role of (1-->3) linkages on the mix-linked xylan hydration-induced conformational rearrangement. The mix-linked xylan signals were observed in the CPMAS NMR spectrum of hydrated residues obtained after extensive extractions by NaOH or strong chaotropic solutions indicating strong hydrogen bonds or covalent linkages. T-1rho relaxations were measured close or above 10 ms for the mix-linked xylan in the dry and hydrated state in AIR and indicated that the overall xylan chains likely remain rigid. Rehydration of the mix-linked xylan lead to a decrease in the motion of protons bounded to the C-1 and C-4 carbons of the (1-->4)-linked xylose supporting the re-organization of the xylan chains under hydration involving junction-zones held by hydrogen bonds between adjacent (1-->4)-linked xylose blocks. The CPMAS NMR spectrum of both dry and rehydrated residues obtained after NaOH and HCl extractions demonstrated the presence of cellulose and (1-->4)-linked xylans. The structures of the different polysaccharides are discussed in relation to their interactions and putative functions on the cell wall mechanical properties in P. palmata. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1559 / 1569
页数:11
相关论文
共 50 条
  • [1] Structural studies of the mix-linked β-(1 → 3)/β-(l → 4)-D-xylans from the cell wall of Palmaria palmata (Rhodophyta)
    Deniaud, E
    Quemener, B
    Fleurence, J
    Lahaye, M
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2003, 33 (1-3) : 9 - 18
  • [2] Initial observations on glycoside deposition in cell walls of Palmaria palmata (L.) Kuntze (Rhodophyta) during spore germination
    Deniaud, Estelle
    Le Gall, Line
    Rusig, Anne-Marie
    Lahaye, Marc
    BOTANICA MARINA, 2006, 49 (03) : 266 - 269
  • [3] Comparison of celery (Apium graveolens L.) collenchyma and parenchyma cell wall polysaccharides enabled by solid-state 13C NMR
    Zujovic, Zoran
    Chen, Da
    Melton, Laurence D.
    CARBOHYDRATE RESEARCH, 2016, 420 : 51 - 57
  • [4] Comparison of leaf and stem cell-wall components in barley straw by solid-state 13C NMR
    Love, GD
    Snape, CE
    Jarvis, MC
    PHYTOCHEMISTRY, 1998, 49 (05) : 1191 - 1194
  • [5] Structural and dynamic study of chemically modified polyHIPE by solid-state 13C NMR spectroscopy
    Mercier, A
    Kuroki, S
    Ando, I
    Deleuze, H
    Mondain-Monval, O
    JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2001, 39 (09) : 956 - 963
  • [6] Quantification of protein secondary structure by 13C solid-state NMR
    Andrade, Fabiana Diuk
    Forato, Lucimara Aparecida
    Bernardes Filho, Rubens
    Colnago, Luiz Alberto
    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2016, 408 (14) : 3875 - 3879
  • [7] Quantitation of aliphatic suberin in Quercus suber L. cork by FTIR spectroscopy and solid-state 13C-NMR spectroscopy
    Lopes, MH
    Neto, CP
    Barros, AS
    Rutledge, D
    Delgadillo, I
    Gil, AM
    BIOPOLYMERS, 2000, 57 (06) : 344 - 351
  • [8] Leaf-fiber lignins of Phormium varieties compared by solid-state 13C NMR spectroscopy
    Newman, RH
    Tauwhare, SEK
    Scheele, S
    Kanawa, RT
    HOLZFORSCHUNG, 2005, 59 (02) : 147 - 152
  • [9] Extensively sparse 13C labeling to simplify solid-state NMR 13C spectra of membrane proteins
    Qiong Tong
    Huan Tan
    Jianping Li
    Huayong Xie
    Yongxiang Zhao
    Yanke Chen
    Jun Yang
    Journal of Biomolecular NMR, 2021, 75 : 245 - 254
  • [10] Extensively sparse 13C labeling to simplify solid-state NMR 13C spectra of membrane proteins
    Tong, Qiong
    Tan, Huan
    Li, Jianping
    Xie, Huayong
    Zhao, Yongxiang
    Chen, Yanke
    Yang, Jun
    JOURNAL OF BIOMOLECULAR NMR, 2021, 75 (6-7) : 245 - 254