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DOI: 10.1055/s-2001-10636
© Georg Thieme Verlag Stuttgart · New York
High Yield of Podophyllotoxin from Leaves of Podophyllum peltatum by In situ Conversion of Podophyllotoxin 4-O-β-D-Glucopyranoside
Publication History
November 4, 1999
January 16, 2000
Publication Date:
31 December 2001 (online)
Abstract
Rehydration of powdered tissues of Podophyllum peltatum L. prior to extraction with an organic solvent allows endogenous β-glucosidases to hydrolyze lignan 4-O-β-D-glucosides in situ and increase the yield of podophyllotoxin. Aqueous extraction of rhizomes and leaves of P. peltatum yielded 4- to 10-fold greater quantities of podophyllotoxin than the traditional ethanolic extraction. Most significantly, leaves were shown to contain over 52 mg of podophyllotoxin per g of dry weight (5.2 %), exceeding levels previously reported from any source. These results point to the use of leaves harvested from cultivated P. peltatum as an attractive alternative to the destructive collection of natural populations.
References
- 1 Foster S. Medicinal plant conservation and generic resources. Examples from the temperate Northern Hemisphere. Acta Horticulturae. 1993; 330 67-73
- 2 Nautiyal M C, Rawat A S, Bhadula S K, Purohit A N. Seed germination in Podophyllum hexandrum . Seed Research. 1987; 15 206-9
- 3 van Uden W, Pras N, Visser J F, Malingré T M. Detection and identification of podophyllotoxin produced by cell cultures derived from Podophyllum hexandrum . Plant Cell Reports. 1989; 8 165-8
- 4 Jackson D E, Dewick P M. Aryltetralin lignans from Podophyllum hexandrum and Podophyllum peltatum . Phytochemistry. 1984; 23 1147-52
- 5 Bastos J K, Burandt C LJr, Nanayakkara N PD, Bryant L, McChesney J DJ. Quantitation of aryltetralin lignans in plant parts and among different populations of Podophyllum peltatum by reversed-phase high-performance liquid chromatography. Journal of Natural Products. 1996; 59 406-8
- 6 Moraes-Cerdeira R M, Burandt C LJr, Bastos J K, Nanayakkara N PD, McChesney J D. In vitro propagation of Podophyllum peltatum L. Planta Medica. 1998; 64 42-5
- 7 Broomhead A J, Dewick P M. Aryltetralin lignans from Linum flavum and Linum capitatum . Phytochemistry. 1990; 29 3839-44
- 8 van Uden W, Bos J A, Boeke G M, Woerdenbag H J, Pras N. The large-scale isolation of deoxypodophyllotoxin form rhizomes of Anthriscum sylvestris followed by its bioconversion into 5 methoxypodophyllotoxin β-D-glucoside in cell culture of Linum flavum . Journal of Natural Products. 1997; 60 401-3
- 9 Broomhead A J, Rahman M MA, Dewick P M, Jackson D E, Lucas J A. Matairesinol as precursor of Podophyllum lignans. Phytochemistry. 1991; 30 1489-92
- 10 Stoll A, Renz J, von Wartburg A. The isolation of podophyllotoxin glucoside. Journal of the American Chemical Society. 1954; 76 3103-4
-
11 Esen A, Gungor G.
Stability and activity of plant and fungal β-glucosidases under denaturing conditions . In: Esen A, editor American Chemical Society, Washington; β-Glucosidases: biochemistry and molecular biology 1993: 214-39
Dr. Franck E. Dayan
USDA, ARS, NPURU
National Center for Natural Products Research
University
MS 38677
USA
Email: fdayan@olemiss.edu
Fax: +1 662 915-1035