Planta Med 2003; 69(3): 285-286
DOI: 10.1055/s-2003-38476
Letter
© Georg Thieme Verlag Stuttgart · New York

Enzymatic Preparation of Ginsenosides Rg2, Rh1, and F1 from Protopanaxatriol-Type Ginseng Saponin Mixture

Sung-Ryong Ko1 , Kang-Ju Choi1 , Kei Uchida2 , Yukio Suzuki2
  • 1KT & G Central Research Institute, Taejon, Korea
  • 2Research Institute for Bioresources, Okayama University, Kurashiki, Japan
Further Information

Publication History

Received: July 17, 2002

Accepted: October 20, 2002

Publication Date:
04 April 2003 (online)

Abstract

During investigations on the hydrolysis of a protopanaxatriol-type saponin mixture by various glycoside hydrolases, it was found that two minor saponins, ginsenosides Rg2 and Rh1, were formed in high yields by crude β-galactosidase from Aspergillus oryzae and crude lactase from Penicillium sp., respectively. Moreover, a crude preparation of naringinase from Penicillium decumbens readily hydrolyzed a protopanaxatriol-type saponin mixture to give an intestinal bacterial metabolite, ginsenoside F1 as the main product. A crude preparation of hesperidinase from Penicillium sp. selectively hydrolyzed ginsenoside Re into ginsenoside Rg1. This is the first report on the enzymatic preparation of minor saponins, ginsenosides Rg2 and Rh1, and of an intestinal bacterial metabolite, ginsenoside F1, with a high efficiency from a protopanaxatriol-type saponin mixture.

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Dr. Sung-Ryong Ko

KT & G Central Research Institute

302 Shinsong-dong

Yusong-ku

Taejon, 305-345, Korea

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