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Microbial transformation of pseudoprotodioscin by Gibberella fujikuroi.
Hu, Hong-Xiu; Gao, Ran-Ran; Gao, Zhao-Hui; Qiao, Yue; Dong, Xin-Ran; Ding, Gang; Sun, Di-An.
Affiliation
  • Hu HX; a Natural Medicine Chemistry Research Center, Institute of Medicinal Plant Development , Chinese Academy of Medical Sciences & Peking Union Medical College , Beijing 100193 , China.
  • Gao RR; a Natural Medicine Chemistry Research Center, Institute of Medicinal Plant Development , Chinese Academy of Medical Sciences & Peking Union Medical College , Beijing 100193 , China.
  • Gao ZH; a Natural Medicine Chemistry Research Center, Institute of Medicinal Plant Development , Chinese Academy of Medical Sciences & Peking Union Medical College , Beijing 100193 , China.
  • Qiao Y; a Natural Medicine Chemistry Research Center, Institute of Medicinal Plant Development , Chinese Academy of Medical Sciences & Peking Union Medical College , Beijing 100193 , China.
  • Dong XR; a Natural Medicine Chemistry Research Center, Institute of Medicinal Plant Development , Chinese Academy of Medical Sciences & Peking Union Medical College , Beijing 100193 , China.
  • Ding G; a Natural Medicine Chemistry Research Center, Institute of Medicinal Plant Development , Chinese Academy of Medical Sciences & Peking Union Medical College , Beijing 100193 , China.
  • Sun DA; a Natural Medicine Chemistry Research Center, Institute of Medicinal Plant Development , Chinese Academy of Medical Sciences & Peking Union Medical College , Beijing 100193 , China.
J Asian Nat Prod Res ; 20(7): 624-632, 2018 Jul.
Article in En | MEDLINE | ID: mdl-29732923
ABSTRACT
Three new (6, 9, and 12) and nine known steroidal saponins were obtained from the fermentation broth of pseudoprotodioscin (PPD) incubated with a fungus Gibberella fujikuroi CGMCC 3.4663. Structures of the metabolites were elucidated by 1-D (1H, 13C), 2-D (HMBC, HSQC, NOESY) NMR, and HR-MS analyses. The biotransformation pathway of pseudoprotodioscin by Gibberella fujikuroi CGMCC 3.4663 was proposed. Compounds 1-11 were tested in vitro for their cytotoxic activities against two human cancer cell lines (HepG2 and Hela). Compounds 1, 6, 9, and 10 exhibited cytotoxic activity against HepG2 cells. Compound 10 exhibited cytotoxicity to Hela cells.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diosgenin / Gibberella Limits: Humans Language: En Journal: J Asian Nat Prod Res Journal subject: BOTANICA / QUIMICA Year: 2018 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diosgenin / Gibberella Limits: Humans Language: En Journal: J Asian Nat Prod Res Journal subject: BOTANICA / QUIMICA Year: 2018 Document type: Article Affiliation country: China