Synthesis of β-Alkyl Glucosides by Enzymic Transglucosylaiton
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概要
- 論文の詳細を見る
Lactase from Kluyveromyces lactis was found to have high transglucosylation activity, transferring the glucosyl group of aryl glucoside to an alcoholic hydroxyl group in high yield. Both primary and secondary alcohols can accept the glucosyl group. Transglucosylation to glycol yielded a single kind of glucoside. A very hydrophilic alcohol, such as glycerol, could not serve as a substrate in this system. Hydrophobic alcohols slightly soluble in water were glucosylated in a two-phase system consisting of water and an organic solvent immiscible with water.
- 公益社団法人日本薬学会の論文
- 1984-03-25
著者
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三尾 直樹
徳島文理大学薬学部
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佐藤 利夫
School of Pharmacy, Tokushima University of Arts and Science
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三尾 直樹
School of Pharmacy, Tokushima University of Arts and Science
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佐藤 利夫
徳島文理大学薬学部薬品製造化学教室
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武市 博
School of Pharmacy, Tokushima University of Arts & Science
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武市 博
School Of Pharmacy Tokushima University Of Arts & Science
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