Structural details of crystalline cellulose from higher plants

被引:164
作者
Sturcová, A
His, I
Apperley, DC
Sugiyama, J
Jarvis, MC [1 ]
机构
[1] Univ Glasgow, Dept Chem, Glasgow G12 8QQ, Lanark, Scotland
[2] Univ Durham, EPSRC Solid State NMR Serv, Durham DH1 3LE, England
[3] Kyoto Univ, Wood Res Inst, Kyoto 6110011, Japan
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1021/bm034517p
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
It is commonly assumed that cellulose from higher plants contains the Ialpha and Ibeta crystalline allomorphs together with surface and disordered chains. For cellulose Ialpha, the evidence for its presence in higher plants is restricted to the C-4 signals in the solid-state C-13 NMR spectrum, which match those of crystalline cellulose Ialpha from algal sources. Algal cellulose Ialpha can be converted to the Ibeta form by high-temperature annealing, We used this approach to generate cellulose samples differing in Ibeta content from flax fibers and celery collenchyma, which respectively are representative of textile (secondary-wall) and primary-wall cellulose. It was then possible to isolate the detailed spectral contributions of the surface, Ibeta and Ialpha-like phases from linear combinations of the observed C-13 NMR and FTIR spectra. The C-13 NMR spectra resembled those of highly crystalline tunicate or algal cellulose Ibeta and Ialpha, with slight differences implying increased disorder and minor conformational discrepancies. The FTIR spectrum of the Ibeta form was closely similar to its more crystalline counterparts, but the FTIR spectrum of the Ialpha form was not. In addition to increased bandwith indicative of lower order, it showed substantial differences in the profile of hydroxyl stretching bands. These results confirm that higher plants synthesize cellulose Ibeta but show that the Ialpha-like chains, although conformationally quite similar to crystalline algal cellulose Ialpha, sit in a different hydrogen-bonding environment in higher plants. The differences are presumably occasioned by the small diameter of the crystallites and the influence of the crystallite surface on chain packing.
引用
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页码:1333 / 1339
页数:7
相关论文
共 49 条
[1]  
ATALLA RH, 1984, SCIENCE, V223, P283, DOI 10.1126/science.223.4633.283
[2]   The role of solid state 13C NMR spectroscopy in studies of the nature of native celluloses [J].
Atalla, RH ;
VanderHart, DL .
SOLID STATE NUCLEAR MAGNETIC RESONANCE, 1999, 15 (01) :1-19
[3]  
Atalla RH., 1983, J APPL POLYM SCI APP, V37, P295
[4]   New insight into cellulose structure by atomic force microscopy shows the Iα crystal phase at near-atomic resolution [J].
Baker, AA ;
Helbert, W ;
Sugiyama, J ;
Miles, MJ .
BIOPHYSICAL JOURNAL, 2000, 79 (02) :1139-1145
[5]   INFRARED AND RAMAN-SPECTROSCOPY OF CARBOHYDRATES .5.NORMAL COORDINATE ANALYSIS OF CELLULOSE 1 [J].
CAEL, JJ ;
GARDNER, KH ;
KOENIG, JL ;
BLACKWELL, J .
JOURNAL OF CHEMICAL PHYSICS, 1975, 62 (03) :1145-1153
[6]   CRYSTALLOGRAPHIC ASPECTS OF SUB-ELEMENTARY CELLULOSE FIBRILS OCCURRING IN THE WALL OF ROSE CELLS CULTURED INVITRO [J].
CHANZY, H ;
IMADA, K ;
MOLLARD, A ;
VUONG, R ;
BARNOUD, F .
PROTOPLASMA, 1979, 100 (3-4) :303-316
[7]   Molecular ordering of cellulose after extraction of polysaccharides from primary cell walls of Arabidopsis thaliana:: a solid-state CP/MAS 13C NMR study [J].
Davies, LM ;
Harris, PJ ;
Newman, RH .
CARBOHYDRATE RESEARCH, 2002, 337 (07) :587-593
[8]   HIGH-RESOLUTION, MAGIC ANGLE SAMPLE SPINNING C-13 NMR OF SOLID CELLULOSE-I [J].
EARL, WL ;
VANDERHART, DL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (09) :3251-3252
[9]   CHARACTERIZATION OF CELLULOSE BY DECONVOLUTING THE OH VALENCY RANGE IN FTIR SPECTRA [J].
FENGEL, D .
HOLZFORSCHUNG, 1992, 46 (04) :283-288
[10]  
Fink HP, 1999, PAPIER, V53, P534