Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/34486
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 18074/20272 (89%)
造访人次 : 4297055      在线人数 : 5306
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://ir.cnu.edu.tw/handle/310902800/34486


    標題: Biotransformation of celastrol to a novel, well-soluble, low-toxic and anti-oxidative celastrol-29-O-beta-glucoside by Bacillus glycosyltransferases
    作者: Chang, Te-Sheng
    Wang, Tzi-Yuan
    Chiang, Chien-Min
    Lin, Yu-Ju
    Chen, Hui-Lien
    Wu, Yu-Wei
    Ting, Huei-Ju
    Wu, Jiumn-Yih
    貢獻者: Natl Univ Tainan, Dept Biol Sci & Technol
    Acad Sinica, Biodivers Res Ctr
    Chia Nan Univ Pharm & Sci, Dept Biotechnol
    Taipei Med Univ, Coll Med Sci & Technol, Grad Inst Biomed Informat
    Taipei Med Univ Hosp, Clin Big Data Res Ctr
    Natl Quemoy Univ, Dept Food Sci
    關鍵字: Celastrol
    Glycosyltransferase
    Bacillus
    Triterpenoid
    Biotransformation
    日期: 2021
    上傳時間: 2023-11-11 11:56:52 (UTC+8)
    出版者: SOC BIOSCIENCE BIOENGINEERING JAPAN
    摘要: Celastrol is a quinone-methide triterpenoid isolated from the root extracts of Tripterygium wilfordii (Thunder god vine). Although celastrol possesses multiple bioactivities, the potent toxicity and rare solubility in water hinder its clinical application. Biotransformation of celastrol using either whole cells or purified enzymes to form less toxic and more soluble derivatives has been proven difficult due to its potent antibiotic and enzyme-conjugation property. The present study evaluated biotransformation of celastrol by four glycosyltransferases from Bacillus species and found one glycosyltransferase (BsGT110) from Bacillus subtilis with significant activity toward celastrol. The biotransformation metabolite was purified and identified as celastrol-29-O-beta-glucoside by mass and nuclear magnetic resonance spectroscopy. Celastrol-29-O-beta-glucoside showed over 53-fold higher water solubility than celastrol, while maintained 50% of the free radical scavenging activity of celastrol. When using zebrafish as the in vivo animal model, celastrol-29-O-beta-glucoside exhibited 50-fold less toxicity than celastrol. To our knowledge, the present study is not only the first report describing the biotransformation of celastrol, but also the first one detailing a new compound, celastrol-29-O-beta-glucoside, that is generated in the biotransformation process. Moreover, celastrol-29-O-beta-glucoside may serve as a potential candidate in the future medicine application due to its higher water solubility and lower toxicity. (C) 2020, The Society for Biotechnology, Japan. All rights reserved.
    關聯: J BIOSCI BIOENG, v.131, n.2, pp.176-182
    显示于类别:[生物科技系(所)] 期刊論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    index.html0KbHTML230检视/开启


    在CNU IR中所有的数据项都受到原著作权保护.

    TAIR相关文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈