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刺桐凝集素中β1----2-D-木糖和α1----3-L-岩藻糖取代的N-连接寡糖。分离、表征及与其他豆科凝集素的比较。

The beta 1----2-D-xylose and alpha 1----3-L-fucose substituted N-linked oligosaccharides from Erythrina cristagalli lectin. Isolation, characterisation and comparison with other legume lectins.

作者信息

Ashford D, Dwek R A, Welply J K, Amatayakul S, Homans S W, Lis H, Taylor G N, Sharon N, Rademacher T W

出版信息

Eur J Biochem. 1987 Jul 15;166(2):311-20. doi: 10.1111/j.1432-1033.1987.tb13516.x.

Abstract

The carbohydrate moieties of Erythrina cristagalli lectin were released as oligosaccharides by hydrazinolysis, followed by N-acetylation and reduction with NaB3H4. Fractionation of the tritium-labelled oligosaccharide mixture by Bio-Gel P-4 column chromatography and high-voltage borate electrophoresis revealed that it is composed of five neutral oligosaccharides. Structural studies by sequential exoglycosidase digestion in combination with methylation analysis and two-dimensional 1H-NMR showed that the major component was the fucose-containing heptasaccharide Man alpha 3(Man alpha 6)(Xyl beta 2)Man beta 4GlcNAc beta 4(Fuc alpha 3)GlcNAcol. This is the first report of such a structure in plant lectins. Small amounts of the corresponding afucosyl hexasaccharide were also identified, as well as three other minor components. The structure of the heptasaccharide shows the twin characteristics of a newly established family of N-linked glycans, found to date only in plants. The characteristics are substitution of the common pentasaccharide core [Man alpha 3(Man alpha 6)Man beta 4GlcNAc beta 4GlcNAc] by a D-xylose residue linked beta 1----2 to the beta-mannosyl residue and an L-fucose residue linked alpha 1----3 to the reducing terminal N-acetylglucosamine residue. The oligosaccharide heterogeneity pattern for Erythrina cristagalli lectin was also found for the lectins from four other Erythrina species and the lectins of two other legumes, Sophora japonica and Lonchocarpus capassa.

摘要

刺桐凝集素的碳水化合物部分通过肼解以寡糖形式释放,随后进行N-乙酰化并用NaB3H4还原。通过Bio-Gel P-4柱色谱法和高压硼酸盐电泳对氚标记的寡糖混合物进行分级分离,结果表明它由五种中性寡糖组成。通过外切糖苷酶顺序消化结合甲基化分析和二维1H-NMR进行的结构研究表明,主要成分是含岩藻糖的七糖Manα3(Manα6)(Xylβ2)Manβ4GlcNAcβ4(Fucα3)GlcNAcol。这是植物凝集素中首次报道这种结构。还鉴定出少量相应的去岩藻糖基六糖以及其他三种次要成分。七糖的结构显示了一个新建立的N-连接聚糖家族的双重特征,迄今为止仅在植物中发现。这些特征是常见的五糖核心[Manα3(Manα6)Manβ4GlcNAcβ4GlcNAc]被一个通过β1----2连接到β-甘露糖基残基的D-木糖残基和一个通过α1----3连接到还原末端N-乙酰葡糖胺残基的L-岩藻糖残基取代。刺桐凝集素的寡糖异质性模式在其他四种刺桐属植物的凝集素以及其他两种豆科植物(槐树和卡帕刺果豆)的凝集素中也被发现。

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