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Re-constructing our models of cellulose and primary cell wall assembly
被引:323
作者:

Cosgrove, Daniel J.
论文数: 0 引用数: 0
h-index: 0
机构:
Penn State Univ, Dept Biol, University Pk, PA 16802 USA Penn State Univ, Dept Biol, University Pk, PA 16802 USA
机构:
[1] Penn State Univ, Dept Biol, University Pk, PA 16802 USA
关键词:
SOLID-STATE NMR;
FREQUENCY GENERATION SPECTROSCOPY;
ARABIDOPSIS-THALIANA;
CASPARIAN STRIP;
HIGHER-PLANTS;
SYNTHASE;
BIOSYNTHESIS;
MICROFIBRILS;
XYLOGLUCAN;
PECTIN;
D O I:
10.1016/j.pbi.2014.11.001
中图分类号:
Q94 [植物学];
学科分类号:
071001 ;
摘要:
The cellulose microfibril has more subtlety than is commonly recognized. Details of its structure may influence how matrix polysaccharides interact with its distinctive hydrophobic and hydrophilic surfaces to form a strong yet extensible structure. Recent advances in this field include the first structures of bacterial and plant cellulose synthases and revised estimates of microfibril structure, reduced from 36 to 18 chains. New results also indicate that cellulose interactions with xyloglucan are more limited than commonly believed, whereas pectin-cellulose interactions are more prevalent. Computational results indicate that xyloglucan binds tightest to the hydrophobic surface of cellulose microfibrils. Wall extensibility may be controlled at limited regions ('biomechanical hotspots') where cellulose-cellulose contacts are made, potentially mediated by trace amounts of xyloglucan.
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页码:122 / 131
页数:10
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