Literature DB >> 11145182

Constitutive beta-glucosidases hydrolyzing ginsenoside Rb1 and Rb2 from human intestinal bacteria.

E A Bae1, S Y Park, D H Kim.   

Abstract

When ginsenoside Rb1 and Rb2 were anaerobically incubated with human intestinal microflora, these ginsenosides were metabolized to 20-O-beta-D-glucopyranosyl-20(S)-protopanaxadiol (compound K) and 20(S)-protopanaxadiol. Several kinds of intestinal bacteria hydrolyzed these ginsenosides. Eubacterium sp., Streptococcus sp. and Bifidobacterium sp., which more potently hydrolyzed gentiobiose than sophorose, metabolized ginsenoside Rb1 to compound K via ginsenoside Rd rather than gypenoside XVII. However, Fusobacterium K-60, which more potently hydrolyzed sophorose than gentiobiose, metabolized to compound K via gypenoside XVII. Ginsenoside Rb2 was also metabolized to compound K via ginsenoside Rd or compound O by human intestinal microflora. Eubacterium sp., Streptococcus sp. and Bifidobacterium sp. metabolized ginsenoside Rb2 to compound K via ginsenoside Rd rather than compound O. Fusobacterium K-60 metabolized ginsenoside Rb2 to compound K via compound O.

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Year:  2000        PMID: 11145182     DOI: 10.1248/bpb.23.1481

Source DB:  PubMed          Journal:  Biol Pharm Bull        ISSN: 0918-6158            Impact factor:   2.233


  51 in total

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Authors:  Ho-Young Shin; Sun-Young Park; Jong Hwan Sung; Dong-Hyun Kim
Journal:  Appl Environ Microbiol       Date:  2003-12       Impact factor: 4.792

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Journal:  Cancer Prev Res (Phila)       Date:  2016-07-21

10.  Compound K induces apoptosis of bladder cancer T24 cells via reactive oxygen species-mediated p38 MAPK pathway.

Authors:  Han Wang; Dandan Jiang; Jing Liu; Shuhong Ye; Shan Xiao; Wenwen Wang; Zhongyan Sun; Yuping Xie; Jihui Wang
Journal:  Cancer Biother Radiopharm       Date:  2013-07-30       Impact factor: 3.099

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