Koizumi K, Tanimoto T, Fujita K, Hara K, Kuwahara N, Kitahata S
Faculty of Pharmaceutical Sciences, Mukogawa Women's University, Nishinomiya, Japan.
Carbohydr Res. 1993 Jan 15;238:75-91. doi: 10.1016/0008-6215(93)87006-e.
Transgalactosylated products of branched cyclodextrins (glucosyl-alpha CD, -beta CD, -gamma CD, and maltosyl-alpha CD, -beta CD, -gamma CD) were synthesized by beta-D-galactosidases from Bacillus circulans and Penicillium multicolor using lactose as a donor substrate and branched CDs as acceptors. Eighteen beta-D-galactosylated branched CDs were isolated and purified by HPLC. Their structures were elucidated by FABMS and 13C NMR spectroscopies, and methylation analysis. The chromatographic behavior of these novel heterogeneous branched CDs on three HPLC columns of different separation modes was compared.
以乳糖为供体底物,支链环糊精(葡萄糖基-α环糊精、-β环糊精、-γ环糊精以及麦芽糖基-α环糊精、-β环糊精、-γ环糊精)为受体,利用来自环状芽孢杆菌和多色青霉的β-D-半乳糖苷酶合成了支链环糊精的转半乳糖基化产物。通过高效液相色谱法分离并纯化了18种β-D-半乳糖基化支链环糊精。通过快原子轰击质谱法、13C核磁共振光谱法以及甲基化分析对其结构进行了阐释。比较了这些新型多相支链环糊精在三种不同分离模式的高效液相色谱柱上的色谱行为。