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麦芽糖基(α-1→6)β-环糊精的酶法合成和结构鉴定

崔波1,2, 金征宇1   

    1. 江南大学食品科学与安全教育部重点实验室, 无锡 214036;
    2. 山东轻工业学院食品与生物工程学院, 济南 250353
  • 收稿日期:2006-04-04 修回日期:1900-01-01 出版日期:2007-02-10 发布日期:2007-02-10
  • 通讯作者: 金征宇

Enzymatic Synthesis and Identification of Maltosyl(α-1→6)β-cyclodextrin

CUI Bo1,2, JIN Zheng-Yu1   

    1. Key Laboratory of Food Science and Safety, Ministry of Education, Southern Youngtze University, Wuxi 214036, China;
    2. College of Food and Biological Engineering, Shandong Institute of Light Industry, Jinan 250353, China
  • Received:2006-04-04 Revised:1900-01-01 Online:2007-02-10 Published:2007-02-10
  • Contact: JIN Zheng-Yu

摘要: 采用地衣芽孢杆菌普鲁蓝酶合成Mal-β-CD, 反应产物体系成分简单, 易于分离, Mal-β-CD的转化率可达到56%.

关键词: β-环糊精, 麦芽糖基(α-1→6)β-环糊精, 地衣芽孢杆菌普鲁蓝酶

Abstract: Cyclodextrins are widely used for various purposes and limited because of it's low solubility. Branched cyclodextrins have attracted more and more attention because of their many advantages such as higher solubility in water. In this study a new method for synthesizing maltosyl(α-1→6)β-cyclodextrin with a high yield was described. Mal-β-CD was synthesized through the reverse reaction of Bacillus licheniformis pullulanase and identified. The factors which affect the formation of maltosyl(α-1→6)β-cyclodextrin were studied and the optimum conditions were obtained as follows: 250 U/g β-CD of enzyme amount, molar ratio of maltose to β-CD 12:1—16:1, a substrate mass fraction of 80%, the pH of reaction mixture 4.5 , reaction temperature 70 ℃ and reaction time 60 h respectively. The product was separated by Sephadex G25 column and further purified by Bio-gel P-2 column. Maltosyl(α-1→6)β-cyclodextrin was identified by IR, ESI-MS and NMR. It was proved to be a effective method to synthesize maltosyl(α-1→6)β-cyclodextrin by using Bacillus licheniformis pullulanase. The yield of Mal-β-CD was about 56% under the optimal conditions.

Key words: β-Cyclodextrins, Maltosyl(α-1→6)β-cyclodextrin, Bacillus licheniformis pullulanase

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