生物学杂志

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人参内生菌Burkholderia sp. GE 17-7制备人参皂苷Rg3的研究

  

  1. 1. 鞍山师范学院 化学与生命科学学院, 鞍山 114007; 2. 国家参茸产品质量监督检验中心, 延吉 133002
  • 出版日期:2019-04-18 发布日期:2019-04-18
  • 通讯作者: 付玉,讲师,博士,研究方向为天然活性物质的生物转化,E-mail:02mi@163.com
  • 作者简介:李俊莹,研究方向为天然活性物质的生物转化,E-mail:1730649484@qq.com
  • 基金资助:
    辽宁省博士启动基金项目(201601316);辽宁省大学生创新创业训练计划项目(201510169008);鞍山师范学院博士启动基金项目(2014B03)

Production of ginsenoside Rg3 by Burkholderia sp.GE 17-7 from ginseng endophytes

  1. 1. College of Chemistry and Life Science, Anshan Normal University, Anshan 114007;2. National Ginseng Products Quality Supervision Inspection Center, Yanji 133002, China
  • Online:2019-04-18 Published:2019-04-18

摘要: 许多研究表明人参皂苷是人参中起主要药效活性的物质,尤其是人参稀有皂苷比人参主皂苷在抗癌、抗心脑血管病、抗糖尿病等方面具有更好的疗效。利用从17年生野山参中分离、筛选获得一株人参内生真菌Burkholderia sp. GE 17-7生物转化人参主皂苷。通过薄层色谱法、高效液相色谱法等方法对人参主皂苷(Rb1、Rb2、Rc、Rd、Re和Rg1)的转化产物进行分离纯化,采用波谱解析及理化常数对其进行结构鉴定。同时,对转化路径进行了分析。结果表明人参内生真菌Burkholderia sp. GE 17-7能够特异性水解原人参二醇型皂苷C-20位糖基,对其内部糖基不具有水解特性。经鉴定其转化产物为人参稀有皂苷Rg3。转化路径为人参皂苷Rb1→人参皂苷Rd→人参稀有皂苷Rg3。人参内生真菌Burkholderia sp. GE 17-7能够特异性制备人参稀有皂苷Rg3,为工业制备人参稀有皂苷提供了新的微生物资源。

关键词: 生物转化, 人参内生菌, 人参皂苷Rg3, 底物特异性, Burkholderia sp.

Abstract: Many investigational studies have shown that ginsenosides are the principal active constituents of ginseng in antioxidant, antineoplastic, anti-inflammatory and biomodulatory processes. In particular, minor ginsenoside monomers, such as F2, Rh2, Rg3 and compound K (CK), have greater antitumor activity than the major ginsenoside monomers Rb1, Rb2, Rc, Rd, Re and Rg1. An endophytic bacterium GE 17-7 strain isolated from ginseng roots for 17 years, belonging to the genus Burkholderia, had been used in converting minor ginsenosides. The major ginsenoside monomers Rb1, Rb2, Rc, Rd, Re and Rg1 were used by strain GE 17-7. Biotransformation products were separated and purified through thin-layer chromatography (TLC) and high performance liquid chromatography (HPLC) analysis and identified by spectral analysis and physical constants. The results indicated that Burkholderia sp. GE 17-7 had specific hydrolytic activity for the outer glucose at the C-20 position in protopanaxadiol-type ginsenosides without hydrolysis of the inner glucose. The final metabolite was ginsenoside Rg3 by nuclear magnetic resonance (NMR) analysis. This suggests that the hydrolytic pathway of ginsenoside Rb1 by strain GE 17-7 was ginsenoside Rb1→ginsenoside Rd→ginsenoside Rg3. We have successfully found a specificity ginsenoside Rg3-producing endophytic bacterium GE 17-7 from ginseng.

Key words: bio-transformation, ginseng endophtes, ginsenoside Rg3, substrate specificity, Burkholderia sp.

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