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Evolution of Xylan Substitution Patterns in Gymnosperms and Angiosperms: Implications for Xylan Interaction with Cellulose

机译:裸子植物和被子植物中木聚糖替代模式的演变:木聚糖与纤维素相互作用的意义。

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摘要

The interaction between cellulose and xylan is important for the load-bearing secondary cell wall of flowering plants. Based on the precise, evenly spaced pattern of acetyl and glucuronosyl (MeGlcA) xylan substitutions in eudicots, we recently proposed that an unsubstituted face of xylan in a 2-fold helical screw can hydrogen bond to the hydrophilic surfaces of cellulose microfibrils. In gymnosperm cell walls, any role for xylan is unclear, and glucomannan is thought to be the important cellulose-binding polysaccharide. Here, we analyzed xylan from the secondary cell walls of the four gymnosperm lineages (Conifer, Gingko, Cycad, and Gnetophyta). Conifer, Gingko, and Cycad xylan lacks acetylation but is modified by arabinose and MeGlcA. Interestingly, the arabinosyl substitutions are located two xylosyl residues from MeGlcA, which is itself placed precisely on every sixth xylosyl residue. Notably, the Gnetophyta xylan is more akin to early-branching angiosperms and eudicot xylan, lacking arabinose but possessing acetylation on alternate xylosyl residues. All these precise substitution patterns are compatible with gymnosperm xylan binding to hydrophilic surfaces of cellulose. Molecular dynamics simulations support the stable binding of 2-fold screw conifer xylan to the hydrophilic face of cellulose microfibrils. Moreover, the binding of multiple xylan chains to adjacent planes of the cellulose fibril stabilizes the interaction further. Our results show that the type of xylan substitution varies, but an even pattern of xylan substitution is maintained among vascular plants. This suggests that 2-fold screw xylan binds hydrophilic faces of cellulose in eudicots, early-branching angiosperm, and gymnosperm cell walls.
机译:纤维素和木聚糖之间的相互作用对于开花植物的承重次级细胞壁很重要。基于在双子叶植物中乙酰基和葡萄糖醛糖基(MeGlcA)木聚糖取代的精确,均匀间隔的模式,我们最近提出了2倍螺旋螺杆中未取代的木聚糖表面可以氢键合到纤维素微纤维的亲水表面。在裸子植物细胞壁中,木聚糖的作用尚不清楚,葡甘露聚糖被认为是重要的纤维素结合多糖。在这里,我们从四个裸子植物谱系(针叶树,银杏,苏铁科植物和Gnetophyta)的次生细胞壁中分析了木聚糖。针叶树,银杏和苏铁木聚糖缺乏乙酰化作用,但被阿拉伯糖和MeGlcA修饰。有趣的是,阿拉伯糖基取代位于MeGlcA的两个木糖基残基上,其本身精确地位于每六个木糖基残基上。值得注意的是,Gnetophyta木聚糖更类似于早期分支的被子植物和杜仲木聚糖,缺乏阿拉伯糖,但在其他木糖基残基上具有乙酰化作用。所有这些精确的取代方式均与裸子植物木聚糖与纤维素亲水表面的结合相容。分子动力学模拟支持2倍螺旋针叶树木聚糖与纤维素微纤维亲水面的稳定结合。而且,多个木聚糖链与纤维素原纤维的相邻平面的结合进一步稳定了相互作用。我们的结果表明,木聚糖替代的类型各不相同,但维管植物之间木聚糖替代的模式仍然保持不变。这表明2倍螺旋木聚糖结合了双子叶植物,早分支被子植物和裸子植物细胞壁中纤维素的亲水面。

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