Levy S, Maclachlan G, Staehelin L A
University of Colorado, Boulder 80309-0347, USA.
Plant J. 1997 Mar;11(3):373-86. doi: 10.1046/j.1365-313x.1997.11030373.x.
Cross-links between cellulose microfibrils and xyloglucan (XG) molecules play a major role in defining the structural properties of plant cell walls and the regulation of growth and development of dicotyledonous plants. How these cross-links are established and how they are regulated has yet to be determined. In a previous study, preliminary data were presented which suggested that the different sidechains of XG may play a role in controlling cellulose microfibril-XG interactions. In this study, this question is addressed directly by analyzing to what extent the different sidechains of pea cell wall XG and nasturtium seed storage XG affect their binding to cellulose microfibrils. Of particular importance to this study are the chemical data indicating that pea XG possesses a trisaccharide sidechain, which is not found in nasturtium XG. To this end, conformational dynamic simulations have been used to predict whether oligosaccharides representative of pea and nasturtium XG can adopt a hypothesized cellulose-binding conformation and which of these XGs exhibits a preferential ability to bind cellulose. Extensive analysis of the conformational forms populated during 300 K and high-temperature Monte Carlo simulations established that a planar, sterically accessible, glucan backbone is essential for optimal cellulose-binding. For the trisaccharide sidechain-containing oligosaccharide as found in pea XG, sidechain orientation appeared to regulate the gradual acquisition of this hypothesized cellulose binding conformation. Thus, conformational forms were identified that included the twisted backbone (non-planar) putative solution form of XG, forms in which the trisaccharide sidechain orientation enables increased backbone planarity and steric accessibility, and finally a planar, sterically accessible, backbone. By applying these conformational requirements for cellulose binding, it has been determined that pea XG possesses a two- to threefold occurrence of the cellulose binding conformation than nasturtium XG. Based on this finding, it was predicted that pea XG would bind to cellulose at a higher rate than nasturtium XG. In vitro binding assays showed that pea XG-avicel binding does indeed occur at a twofold higher rate than nasturtium XG-avicel binding. The enhanced ability of pea cell wall XG over nasturtium seed storage XG to associate with cellulose is consistent with a structural role of the former during epicotyl growth where efficient association with cellulose is a requirement. In contrast, the relatively low ability of nasturtium XG to bind cellulose is consistent with the need to enhance the accessibility of this polymer to glycanases during germination. These findings suggest potential roles for XG sidechain substitution, enabling XG to function in a variety of different biological contexts.
纤维素微纤丝与木葡聚糖(XG)分子之间的交联在决定植物细胞壁的结构特性以及双子叶植物生长发育的调控中起着主要作用。这些交联是如何建立的以及如何被调控尚待确定。在之前的一项研究中,初步数据表明XG的不同侧链可能在控制纤维素微纤丝与XG的相互作用中发挥作用。在本研究中,通过分析豌豆细胞壁XG和旱金莲种子储存XG的不同侧链在多大程度上影响它们与纤维素微纤丝的结合,直接解决了这个问题。对本研究特别重要的是化学数据表明豌豆XG具有一种三糖侧链,而在旱金莲XG中未发现这种侧链。为此,已使用构象动力学模拟来预测代表豌豆和旱金莲XG的寡糖是否能采用假定的纤维素结合构象,以及这些XG中哪一种表现出优先结合纤维素的能力。对在300 K和高温蒙特卡洛模拟过程中出现的构象形式进行的广泛分析表明,一个平面的、空间可及的葡聚糖主链对于最佳纤维素结合至关重要。对于豌豆XG中发现的含三糖侧链的寡糖,侧链取向似乎调节了这种假定的纤维素结合构象的逐步获得。因此,鉴定出的构象形式包括XG的扭曲主链(非平面)假定溶液形式、三糖侧链取向使主链平面度和空间可及性增加的形式,以及最终的平面、空间可及的主链。通过应用这些纤维素结合的构象要求,已确定豌豆XG具有纤维素结合构象的发生率是旱金莲XG的两到三倍。基于这一发现,预测豌豆XG与纤维素结合的速率会高于旱金莲XG。体外结合试验表明,豌豆XG与微晶纤维素的结合速率确实比旱金莲XG与微晶纤维素的结合速率高两倍。豌豆细胞壁XG与旱金莲种子储存XG相比,与纤维素结合能力的增强与前者在上胚轴生长过程中的结构作用一致,在上胚轴生长中与纤维素的有效结合是必要的。相反,旱金莲XG结合纤维素的能力相对较低与在萌发过程中提高这种聚合物对聚糖酶的可及性的需求一致。这些发现表明XG侧链取代具有潜在作用,使XG能够在各种不同的生物学环境中发挥作用。