Division of Glycoscience, School of Biotechnology, KTH Royal Institute of Technology, AlbaNova University Centre, 106 91 Stockholm, Sweden.
Wallenberg Wood Science Centre, Department of Fiber and Polymer Technology, School of Chemical Engineering, KTH Royal Institute of Technology, 100 44 Stockholm, Sweden.
Plant Physiol. 2017 Dec;175(4):1579-1592. doi: 10.1104/pp.17.01184. Epub 2017 Oct 25.
Xylan is tightly associated with cellulose and lignin in secondary plant cell walls, contributing to its rigidity and structural integrity in vascular plants. However, the molecular features and the nanoscale forces that control the interactions among cellulose microfibrils, hemicelluloses, and lignin are still not well understood. Here, we combine comprehensive mass spectrometric glycan sequencing and molecular dynamics simulations to elucidate the substitution pattern in softwood xylans and to investigate the effect of distinct intramolecular motifs on xylan conformation and on the interaction with cellulose surfaces in Norway spruce (). We confirm the presence of motifs with evenly spaced glycosyl decorations on the xylan backbone, together with minor motifs with consecutive glucuronation. These domains are differently enriched in xylan fractions extracted by alkali and subcritical water, which indicates their preferential positioning in the secondary plant cell wall ultrastructure. The flexibility of the 3-fold screw conformation of xylan in solution is enhanced by the presence of arabinofuranosyl decorations. Additionally, molecular dynamic simulations suggest that the glycosyl substitutions in xylan are not only sterically tolerated by the cellulose surfaces but that they increase the affinity for cellulose and favor the stabilization of the 2-fold screw conformation. This effect is more significant for the hydrophobic surface compared with the hydrophilic ones, which demonstrates the importance of nonpolar driving forces on the structural integrity of secondary plant cell walls. These novel molecular insights contribute to an improved understanding of the supramolecular architecture of plant secondary cell walls and have fundamental implications for overcoming lignocellulose recalcitrance and for the design of advanced wood-based materials.
木聚糖与植物次生细胞壁中的纤维素和木质素紧密结合,有助于其在维管植物中的刚性和结构完整性。然而,控制纤维素微纤维、半纤维素和木质素之间相互作用的分子特征和纳米力仍未得到很好的理解。在这里,我们结合全面的质谱聚糖测序和分子动力学模拟,阐明了软木木聚糖的取代模式,并研究了不同的分子内基序对木聚糖构象以及对挪威云杉()纤维素表面相互作用的影响。我们证实了木聚糖主链上存在均匀分布的糖基化修饰的基序,以及少量连续发生葡萄糖醛酸化的基序。这些结构域在通过碱和亚临界水提取的木聚糖馏分中具有不同的富集度,这表明它们在次生植物细胞壁超微结构中优先定位。阿拉伯呋喃糖基化修饰增强了木聚糖在溶液中 3 重螺旋构象的灵活性。此外,分子动力学模拟表明,木聚糖中的糖基取代不仅受到纤维素表面的空间位阻容忍,而且增加了对纤维素的亲和力,并有利于 2 重螺旋构象的稳定。与亲水表面相比,这种效应在疏水面上更为显著,这证明了非极性驱动力对次生植物细胞壁结构完整性的重要性。这些新的分子见解有助于提高对植物次生细胞壁超分子结构的理解,并对克服木质纤维素的顽固性和设计先进的木材基材料具有重要意义。