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重构我们的纤维素和初生细胞壁组装模型。

Re-constructing our models of cellulose and primary cell wall assembly.

作者信息

Cosgrove Daniel J

机构信息

Department of Biology, Penn State University, University Park, PA 16802, USA.

出版信息

Curr Opin Plant Biol. 2014 Dec;22:122-131. doi: 10.1016/j.pbi.2014.11.001.

Abstract

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.

摘要

纤维素微原纤维比人们普遍认为的更为精妙。其结构细节可能会影响基质多糖如何与其独特的疏水和亲水表面相互作用,从而形成一种坚固但可延展的结构。该领域的最新进展包括细菌和植物纤维素合酶的首个结构,以及对微原纤维结构的修订估计,从36条链减少到18条链。新结果还表明,纤维素与木葡聚糖的相互作用比通常认为的更为有限,而果胶与纤维素的相互作用则更为普遍。计算结果表明,木葡聚糖与纤维素微原纤维的疏水表面结合最紧密。细胞壁的延展性可能在纤维素与纤维素接触的有限区域(“生物力学热点”)受到控制,这可能由痕量的木葡聚糖介导。

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