Hase S, Hara S, Matsushima Y
J Biochem. 1979 Jan;85(1):217-20. doi: 10.1093/oxfordjournals.jbchem.a132314.
Potential aldehyde groups of several monosaccharides and oligosaccharides were coupled with 2-aminopyridine by reductive amination with sodium cyanoborohydride. The product was isolated by adsorption on a Dowex 50 (H+) column, followed by washing, elution with aqueous ammonia and evaporation. The specimen was analyzed by paper electrophoresis at pH 5.0. Each sugar derivative gave a single spot in addition to one corresponding to excess 2-amino-pyridine when the paper was scanned under a UV lamp. The migration rates of these fluorescent sugars were related to their molecular weights and were independent of their linkage points and anomeric configurations. The reducing end sugar units of oligosaccharide derivatives could be identified by gas-liquid chromatography after hydrolysis of the 2-aminopyridine derivatives of the oligosaccharides.
几种单糖和寡糖的潜在醛基通过用氰基硼氢化钠进行还原胺化反应与2-氨基吡啶偶联。产物通过吸附在Dowex 50(H +)柱上进行分离,随后进行洗涤,用氨水洗脱并蒸发。在pH 5.0条件下通过纸电泳对样品进行分析。当在紫外灯下扫描滤纸时,每种糖衍生物除了对应于过量2-氨基吡啶的斑点外还给出一个单一斑点。这些荧光糖的迁移率与其分子量有关,并且与其连接点和异头构型无关。寡糖衍生物的还原端糖单元在寡糖的2-氨基吡啶衍生物水解后可通过气液色谱法鉴定。