L-Ascorbic acid α-glucoside formed by regioselective transglucosylation with rat intestinal and rice seed α-glucosidases : Its improved stability and structure determination

  • 山本 格
    Department of Immunochemistry, Faculty of Pharmaceutical Science, Okayama University
  • 武藤 徳男
    Department of Immunochemistry, Faculty of Pharmaceutical Science, Okayama University
  • 村上 公基
    Department of Immunochemistry, Faculty of Pharmaceutical Science, Okayama University
  • 菅 貞治
    Department of Immunochemistry, Faculty of Pharmaceutical Science, Okayama University
  • 山口 久夫
    Teijin Institute for Bio-Medical Research

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The definite structure and chemical stability of a new glucoside of L-ascorbic acid (AA) which was enzymatically glucosylated with rat intestinal and rice seed α-glucosidases were reported. The stability of this AA derivative in water under aerobic conditions was proved by its remarkable resistance against enhanced oxidative degradation by heat, Cu^<2+> ion or ascorbate oxidase, and it was found to have no reducing activity toward radicals. These properties were obviously distinguishable from those of AA. This glucoside was effectively hydrolyzed by α-glucosidases which possessed the ability to synthesize itself, resulting in the liberation of AA activity. The conjugate was composed of equimoles of AA and glucose. Nuclear magnetic resonance spectra, mass spectra, pH profiles of ultraviolet spectra and pK_a value of 3.10 supported the coupling of α-glucose to the 2-position of AA.From these results, its structure was assigned 2-O-α-D-glucopyranosyl-L-ascorbic acid, being distinct from 6-O-α-D-glucopyranosyl-L-ascorbic acid formed with Aspergillus niger α-glucosidase. These findings indicate that the 2-O-glucoside formed by regioselective transglucosylation withstands oxidateive degradation even in aqueous solutions and it can be used as an available active AA source for multicomponent liquid products.

収録刊行物

  • Chem Pharm Bull

    Chem Pharm Bull 38 3020-3023, 1990

    公益社団法人日本薬学会

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詳細情報 詳細情報について

  • CRID
    1572543027345341824
  • NII論文ID
    110003628206
  • NII書誌ID
    AA00602100
  • ISSN
    00092363
  • 本文言語コード
    en
  • データソース種別
    • CiNii Articles

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