Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/34895
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    CNU IR > Offices > 456 >  Item 310902800/34895
    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/34895


    Title: Novel Ganoderma triterpenoid saponins from the biotransformation-guided purification of a commercial Ganoderma extract
    Authors: Ding, Hsiou-Yu
    Wang, Tzi-Yuan
    Wu, Jiumn-Yih
    Zhang, Yun-Rong
    Chang, Te-Sheng
    Contributors: Chia Nan Univ Pharm & Sci, Dept Cosmet Sci
    Acad Sinica, Biodivers Res Ctr
    Natl Quemoy Univ, Dept Food Sci
    Natl Univ Tainan, Dept Biol Sci & Technol
    Keywords: Ganoderma lucidum
    Glycosyltransferase
    Biotransformation
    Glycosylation
    Triterpenoid]
    Date: 2023
    Issue Date: 2024-12-25 11:05:14 (UTC+8)
    Publisher: SOC BIOSCIENCE BIOENGINEERING JAPAN
    Abstract: Ganoderma sp. contains high amounts of diverse triterpenoids; however, few triterpenoid saponins could be isolated from the medicinal fungus. To produce novel Ganoderma triterpenoid saponins, biotransformation-guided purification (BGP) process was applied to a commercial Ganoderma extract. The commercial Ganoderma extract was partially separated into three fractions by preparative high-performance liquid chromatography, and the separated fractions were then directly biotransformed by a Bacillus glycosyltransferase (BsUGT489). One of the biotransformed products could be further purified and identified as a novel saponin: ganoderic acid C2 (GAC2)-3-O-ll-glucoside by nucleic magnetic resonance (NMR) and mass spectral analyses. Based on the structure of the saponin, the predicted precursor should be the GAC2, which was confirmed to be biotransformed into four saponins, GAC2-3-O-ll-glucoside, GAC2-3,15-Oll-diglucoside and two unknown GAC2 monoglucosides, revealed by NMR and mass spectral analyses. GAC2-3-O-llglucoside and GAC2-3,15-O-ll-diglucoside possessed 17-fold and 200-fold higher aqueous solubility than that of GAC2, respectively. In addition, GAC2-3-O-ll-glucoside retained the most anti-a-glucosidase activity of GAC2 and was comparable with that of the anti-diabetes drug (acarbose). The present study showed that the BGP process is an efficient strategy to survey novel and bioactive molecules from crude extracts of natural products. (c) 2023, The Society for Biotechnology, Japan. All rights reserved.
    Relation: Journal of Bioscience And Bioengineering, v.135, n.5, pp.402-410
    Appears in Collections:[Offices] 456

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