Planta Med 1989; 55(5): 409-416
DOI: 10.1055/s-2006-962054
Review

© Georg Thieme Verlag Stuttgart · New York

The Production of Secondary Metabolites by Plant Cells Cultivated in Bioreactors1

Wolfgang Kreis, Ernst Reinhard
  • Pharmaceutical Institute, University of Tübingen, D-7400 Tübingen, Federal Republic of Germany
1 Presented as a Plenary Lecture at the “International Conference on Plant Science and its Relevance to the Future”, Delhi, India, March 1988
Further Information

Publication History

1988

Publication Date:
24 January 2007 (online)

Abstract

Plant cell cultures are a potential source of pharmaceutically important plant metabolites. In the past few years a lot of success has been achieved in the field of the cultivation of plant cells on a large scale. Special bioreactor systems, such as airlift or drum-type fermentors have been devised for the mass cultivation of plant cells. Classical stirred-tank bioreactors (up to 75000 l volume) have also been used for the cultivation of plant cells and the production of important plant metabolites. Plant cells proliferate much slower than microbial cells. In consequence, the time taken to grow a plant cell suspension from the shake-flask level (300 ml) to the production scale (20,000 l) takes about 3 to 6 weeks. Nevertheless, the cost analyses available show that the production of valuable chemicals by a suitable plant cell culture process could be commercially viable. Plant cells have been grown in batch and repeated batch culture, and single- stage as well as two-stage processes have been developed for the production of secondary metabolites by fermentor-cultured plant cells. There are, however, only few cell culture processes that have attracted industrial attention as yet. Biological rather than technological problems are the main obstacles to a more common use of fermentor-cultured plant cells in industry.