Original ArticlePharmacognosy MagazineVol. 8 | Issue 30 | 2012 | pp. 124–128Open access
Biotransformation of furannoligularenone by transgenic crown galls of Panax quinquefolium
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- 1 Department of Natural Medicinal Chemistry, College of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, China.
- 2 Biotechnology Institute of Chinese Materia Medica, Jinan University, Guangzhou, China.
- 3 Center of Forecasting and Analysis, Shenzhen Institute for Drug Control, Shenzhen, China.
Published in Pharmacognosy Magazine
Correspondence: Rongmin Yu
Center of Forecasting and Analysis, Shenzhen Institute for Drug Control, Shenzhen, China.
Email: tyrm@jnu.edu.cn
Copyright: © 2012 Manuscript Technomedia. This is an open access article.
- Published:
- May 23, 2012
- Received:
- Aug 12, 2011
How to cite
Yan, C., Wang, J., Duan, G., & Yu, R. (2012). Biotransformation of furannoligularenone by transgenic crown galls of Panax quinquefolium. Pharmacognosy Magazine, 8(30), 124–128. https://doi.org/10.4103/0973-1296.96555
Abstract
Background: Transgenic plant suspension cultures could be used as an effective tool for the biotransformation of exogenous compounds. Objective: To investigate the biotransformation of furannoligularenone (1) by transgenic crown galls of Panax quinquefolium. Materials and Methods: Compound 1 was administered into the crown gall cultures and co- cultured for 6 days. The cultures were dried and extracted with methanol for HPLC analyses. The extract was separated on column chromatography, and biotransformation products’ structures were elucidated by the physicochemical properties and the data of NMR and MS. Moreover, three flasks were randomly chosen each day to establish time–course during the period for co- culturing. Results: Co-culturing compound 1 with crown galls yielded two compounds, 3-oxo- eremophila-1,7(11)-dien-12,8-olide (2) and 3-oxo-8-hydroxy-eremophila-1,7(11)-dien-12,8-olide (3), which were obtained by biotransformation using P. quinquefolium crown galls for the first time. Time–course investigation revealed that the mole conversion ratio reached the highest level of 45.5% and 33.9% on fourth and fifth day after substrate administration, respectively. Furthermore, a proposal biosynthesis pathway was given from compound 1 to compounds 2 and 3. Conclusion: This was the first example of compound 1 being successfully converted into compounds 2 and 3 by transgenic crown galls of P. quinquefolium.
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Article metadata
| Title | Biotransformation of furannoligularenone by transgenic crown galls of Panax quinquefolium |
|---|---|
| Authors | Chunyan Yan; Jue Wang; Guoyan Duan; Rongmin Yu |
| Affiliations | Department of Natural Medicinal Chemistry, College of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, China.; Biotechnology Institute of Chinese Materia Medica, Jinan University, Guangzhou, China.; Center of Forecasting and Analysis, Shenzhen Institute for Drug Control, Shenzhen, China. |
| Corresponding author | tyrm@jnu.edu.cn |
| Journal | Pharmacognosy Magazine |
| Volume / Issue | Vol. 8, Issue 30 (2012) |
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