Please use this identifier to cite or link to this item:
|Title:||Plants as Bioreactor|
|Series/Report no.:||<b>Int. cl. <sup>7</sup>— </b>A61K 39/00, C12N 5/00, C12N 15/00|
|Abstract:||Production of pharmaceutically useful plant secondary metabolites <i>in vitro</i> has various advantages compared to extraction of these compounds from plants grown in the field or collected in nature. Exact control of various environmental parameters ensures a reproducible quality of the material totally independent from climate, weather and pests that affect severely the quality of plant material grown in nature. Thus, much research has been done to establish plant cell and suspension cultures for metabolite production. However, undifferentiated cell cultures often do not produce the desired metabolites in considerable amounts or lose their production capacity over a period of time. In contrast, <i>in vitro</i> cultures of fully differentiated plant organs exhibit a high and reliable production capacity of plant secondary metabolites. Thus, special bioreactors working according to the temporary immersion principle have been designed for automated <i>in vitro</i> culture of fully differentiated plant organs. It has been demonstrated that shoots, roots as well as tubers can be grown successfully with high multiplication rates in these bioreactors. Moreover, it has been found that metabolite concentrations in these tissues are much higher compared to undifferentiated cell cultures. Control of <i>in vitro</i> environmental parameters such as medium supplements, light conditions, immersion frequencies and gas composition have been used successfully to modify the metabolite content of the produced plant biomass. This is a very promising strategy for production of pharmaceutically active plant biomass <i>in vitro</i>.|
|ISSN:||0975-1092 (Online); 0972-592X (Print)|
|Appears in Collections:||NPR Vol.3(6) [November-December 2004]|
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.