Microfibril diameter in celery collenchyma cellulose:: X-ray scattering and NMR evidence

被引:96
作者
Kennedy, Craig J. [1 ]
Cameron, Graeme J.
Sturcova, Adriana
Apperley, David C.
Altaner, Clemens
Wess, Timothy J.
Jarvis, Michael C.
机构
[1] Univ Glasgow, Dept Chem, Glasgow G12 8QQ, Lanark, Scotland
[2] Univ Cardiff Wales, Struct Biophys Grp, Sch Optometry & Vis Sci, Cardiff CF10 3NB, Wales
[3] Univ Stirling, Dept Comp Sci, Stirling FK9 4LA, Scotland
[4] Univ Durham, Dept Chem, Durham DH1 3LE, England
基金
英国工程与自然科学研究理事会;
关键词
cellulose; crystallinity; cell walls; microfibrils; SAXS; WAXS; NMR;
D O I
10.1007/s10570-007-9116-1
中图分类号
TB3 [工程材料学]; TS [轻工业、手工业、生活服务业];
学科分类号
0805 ; 080502 ; 0822 ;
摘要
Cellulose isolated from celery collenchyma is typical of the low-crystallinity celluloses that can be isolated from primary cell-walls of higher plants, except that it is oriented with high uniformity. The diameter of the microfibrils of celery collenchyma cellulose was estimated by three separate approaches: C-13 NMR measurement of the ratio of surface to interior chains; estimation of the dimensions of the crystalline lattice from wide angle X-ray scattering (WAXS) measurements using the Scherrer equation; and the observation that microfibrils of this form of cellulose have the unusual property of packing into an irregular array from which small angle X-ray scattering (SAXS) shows features of both form and interference functions. The interference function contributing to the SAXS pattern implied a mean microfibril centre-to-centre distance of 3.6 nm, providing an upper limit for the diameter. However modelling of the scattering pattern from an irregular array of microfibrils showed that the observed scattering curve could be matched at a range of diameters down to 2.4 nm, with the intervening space more or less sparsely occupied by hemicellulose chains. The lateral extent of the crystalline lattice normal to the 200 plane was estimated as a minimum of 2.4 nm by WAXS through the Scherrer equation, and a diameter of 2.6 nm was implied by the surface: volume ratio determined by C-13 NMR. The WAXS and NMR measurements both depended on the assumption that the surface chains were positioned within an extension of the crystalline lattice. The reliability of this assumption is uncertain. If the surface chains deviated from the lattice, both the WAXS and the NMR data would imply larger microfibril diameters within the range consistent with the SAXS pattern. The evidence presented is therefore all consistent with microfibril diameters from about 2.4 to 3.6 nm, larger than has previously been suggested for primary-wall cellulose. Some degree of aggregation may have occurred during the isolation of the cellulose, but the larger microfibril diameters within the range proposed are a consequence of the novel interpretation of the experimental data from WAXS and NMR and are consistent with previously published data if these are similarly interpreted.
引用
收藏
页码:235 / 246
页数:12
相关论文
共 45 条
[1]  
Abramovitz M., 1970, HDB MATH FUNCTIONS
[2]   A small-angle X-ray scattering study of the effect of hydration on the microstructure of flax fibers [J].
Astley, OM ;
Donald, AM .
BIOMACROMOLECULES, 2001, 2 (03) :672-680
[3]  
ATALLA RH, 1984, SCIENCE, V223, P283, DOI 10.1126/science.223.4633.283
[4]   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
[5]   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
[6]   Solid-state 13C-NMR spectroscopy shows that the xyloglucans in the primary cell walls of mung bean (Vigna radiata L.) occur in different domains:: a new model for xyloglucan-cellulose interactions in the cell wall [J].
Bootten, TJ ;
Harris, PJ ;
Melton, LD ;
Newman, RH .
JOURNAL OF EXPERIMENTAL BOTANY, 2004, 55 (397) :571-583
[7]   A small angle X-ray scattering study of pore structure in Tencel® cellulose fibres and the effects of physical treatments [J].
Crawshaw, J ;
Cameron, RE .
POLYMER, 2000, 41 (12) :4691-4698
[8]   Atomic force microscopy of microfibrils in primary cell walls [J].
Davies, LM ;
Harris, PJ .
PLANTA, 2003, 217 (02) :283-289
[9]  
EIKENBERRY EF, 1982, INT J BIOL MACROMOL, V4, P322, DOI 10.1016/0141-8130(82)90063-0
[10]  
Evans R, 2001, FOREST PROD J, V51, P53