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CH区域中双糖的振动圆二色性(VCD)研究:朝向糖苷键位置的鉴别

Vibrational circular dichroism (VCD) studies on disaccharides in the CH region: toward discrimination of the glycosidic linkage position.

作者信息

Taniguchi Tohru, Monde Kenji

机构信息

Laboratory of Advanced Chemical Biology, Graduate School of Advanced Life Science, Frontier Research Center for Post-Genome Science and Technology, Hokkaido University, Kita-ku, Sapporo 001-0021, Japan.

出版信息

Org Biomol Chem. 2007 Apr 7;5(7):1104-10. doi: 10.1039/b618841a. Epub 2007 Mar 5.

Abstract

The structural features of carbohydrates are a combination of 1) sequence and types of mono-sugars, 2) stereochemistry of their glycosidic linkages, and 3) their glycosidic linkage sites. We performed the first systematic VCD study on glycoside linking site discrimination. VCD spectra, in the CH stretching region from 2000 to 4000 cm(-1), of eleven glucobioses (trehalose (alpha1-alpha1), neotrehalose (alpha1-beta1), isotrehalose (beta1-beta1), kojibiose (alpha1-2), nigerose (alpha1-3), maltose (alpha1-4), isomaltose (alpha1-6), sophorose (beta1-2), laminaribiose (beta1-3), cellobiose (beta1-4), gentiobiose (beta1-6)) suggested a possible new discrimination method for glyco analysis, while VCD spectra in the mid-IR region distinguished the stereochemistry (alpha or beta) of the glycosidic linkage. Both reducing and nonreducing glucobioses showed different VCD spectral features compared to their constituent D-glucose and the anomer-fixed model compounds. Interresidue interaction such as hydrogen bonding was suggested to cause these spectral differences. Interplay between residues is a common phenomenon and thus VCD analysis could be applicable to other di-, oligo- or poly-saccharides. Several isotropic labeled compounds were also measured to support spectral assignment and interpretation.

摘要

碳水化合物的结构特征由以下三方面组合而成

1)单糖的序列和类型;2)糖苷键的立体化学;3)糖苷键连接位点。我们首次对糖苷连接位点鉴别进行了系统的振动圆二色性(VCD)研究。在11种葡萄糖二糖(海藻糖(α1-α1)、新海藻糖(α1-β1)、异海藻糖(β1-β1)、曲二糖(α1-2)、黑曲霉糖(α1-3)、麦芽糖(α1-4)、异麦芽糖(α1-6)、槐糖(β1-2)、昆布二糖(β1-3)、纤维二糖(β1-4)、龙胆二糖(β1-6))的2000至4000 cm⁻¹ 的C-H伸缩区域的VCD光谱表明,这可能是一种用于糖分析鉴别的新方法,而中红外区域的VCD光谱则可区分糖苷键的立体化学(α或β)。与它们的组成成分D-葡萄糖和端基异构体固定的模型化合物相比,还原性和非还原性葡萄糖二糖均呈现出不同的VCD光谱特征。推测诸如氢键等残基间相互作用导致了这些光谱差异。残基间的相互作用是一种常见现象,因此VCD分析可能适用于其他二糖、寡糖或多糖。还测量了几种同位素标记化合物以辅助光谱归属和解释。

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