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云杉木材中纤维素微纤丝的纳米结构。

Nanostructure of cellulose microfibrils in spruce wood.

机构信息

Centre for Plant Integrative Biology, University of Nottingham, Sutton Bonnington Campus, Leicestershire LE12 5RD, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 2011 Nov 22;108(47):E1195-203. doi: 10.1073/pnas.1108942108. Epub 2011 Nov 7.

Abstract

The structure of cellulose microfibrils in wood is not known in detail, despite the abundance of cellulose in woody biomass and its importance for biology, energy, and engineering. The structure of the microfibrils of spruce wood cellulose was investigated using a range of spectroscopic methods coupled to small-angle neutron and wide-angle X-ray scattering. The scattering data were consistent with 24-chain microfibrils and favored a "rectangular" model with both hydrophobic and hydrophilic surfaces exposed. Disorder in chain packing and hydrogen bonding was shown to increase outwards from the microfibril center. The extent of disorder blurred the distinction between the I alpha and I beta allomorphs. Chains at the surface were distinct in conformation, with high levels of conformational disorder at C-6, less intramolecular hydrogen bonding and more outward-directed hydrogen bonding. Axial disorder could be explained in terms of twisting of the microfibrils, with implications for their biosynthesis.

摘要

尽管木质生物质中纤维素含量丰富,且其对于生物学、能源和工程领域都至关重要,但木材中纤维素微纤维的结构仍不为人知。本研究采用一系列光谱方法结合小角中子和广角 X 射线散射,对云杉木材纤维素的微纤维结构进行了研究。散射数据与 24 链微纤维一致,并支持具有疏水性和亲水性表面暴露的“矩形”模型。从微纤维中心向外,链包装和氢键的无序度增加。无序的程度模糊了 Iα和 Iβ两种同晶型之间的区别。表面的链在构象上是不同的,在 C-6 处具有高水平的构象无序,分子内氢键较少,向外指向的氢键较多。轴向无序可以用微纤维的扭曲来解释,这对它们的生物合成有影响。

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