Planta Med 2002; 68(5): 420-424
DOI: 10.1055/s-2002-32082
Original Paper
Biochemistry, Physiology, in vitro-cultures
© Georg Thieme Verlag Stuttgart · New York

Efficient Paclitaxel Production using Protoplasts Isolated from Cultured Cells of Taxus cuspidata

Hideki Aoyagi1 , Frank DiCosmo2, 3, 4 , Hideo Tanaka1
  • 1Institute of Applied Biochemistry, University of Tsukuba, Tsukuba, Ibaraki, Japan
  • 2Department of Botany, University of Toronto, Toronto, Ontario, Canada
  • 3Institute of Biomedical Engineering, University of Toronto, Toronto, Ontario, Canada
  • 4Department of Surgery, University of Toronto, Toronto, Ontario, Canada
Further Information

Publication History

July 23, 2001

November 18, 2001

Publication Date:
07 June 2002 (online)

Abstract

Efficient isolation of protoplasts from Taxus cuspidata cultured cells, localization of paclitaxel in the cultured cells, and efficient production of paclitaxel by protoplasts were studied. Hemicellulase, potassium citric acid solution, and degassing treatments were effective in increasing the yield of protoplasts isolated from T. cuspidata cultured cells. Protoplasts yields (3.2 - 6.4 × 106 number/g-fresh weight cells) were achieved by combining the various treatments with specific culture and cell phases. It was found that about 30 % and 35 % of paclitaxel in the cells was located in cell walls and/or between the cell wall and cell membrane (CW) of suspension cells in the growth phase and in the stationary phase, respectively. About 30 % and 43 % of paclitaxel in the cells was located in CW of the cells grown in solid culture in growth phase and in the stationary phase, respectively. In comparison with cell suspension culture, protoplasts in a static culture and the protoplasts immobilized in agarose gel in shaking culture resulted to about 6 times increase in the extracellular paclitaxel accumulation.

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Prof. Hideo Tanaka

Institute of Applied Biochemistry

University of Tsukuba

Tsukuba

Ibaraki 305-8572

Japan

Email: hitanaka@sakura.cc.tsukuba.ac.jp

Fax: +81-298-534605

Phone: +81-298-534609

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