Abstract
Cryopreservation experiments were performed with cell suspension cultures of the following species: Atriplex hortensis L.,.A, litoralis L. (Chenopodiaceae), Berberis wilsoniae HEMSL. & WILS. (Berberidaceae), Coleus blumei BENTH. (Lamiaceae), Daucus carota L. (Apiaceae), Digitalis lanata EHRH. (Scrophulariaceae), and Panax ginseng C.A. MEY. (Araliaceae), The protocol comprises a preculture phase in nutrient media with enhanced osmolarity, treatment with cryoprotectants, slow freezing, storage at -196°C, rapid thawing, and post-thaw treatments. Biochemical capacities remain unchanged in frozen-thawed cultures. This was shown to be the case in D. carota, D. lanata, and P. ginseng. A survey on literature concerning this point is presented. Some alternatives to the standard cryopreservation procedure are given. Experiments are underway to investigate the physiological events during the preculture phase. As a consequence of osmotic stress cell viability decreased to a certain extent. A suspension of this process and even recovery have been observed in the cases of positive response. Further events such as the uptake of preculture additives and changes in the cytoplasm: vacuole volume ratio will be discussed.
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© 1990 Kluwer Academic Publishers
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Seitz, U., Banspach, D., Göldner, E., Reinhard, E. (1990). Cryopreservation of Plant Cell Cultures. In: Sangwan, R.S., Sangwan-Norreel, B.S. (eds) The Impact of Biotechnology on Agriculture. Current Plant Science and Biotechnology in Agriculture, vol 8. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-0587-0_28
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DOI: https://doi.org/10.1007/978-94-009-0587-0_28
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