Cryopreservation of embryogenic suspension cultures of Cyclamen persicum Mill

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Original languageEnglish
Pages (from-to)1-8
Number of pages8
JournalPlant cell reports
Volume23
Issue number1-2
Publication statusPublished - 25 May 2004

Abstract

We have developed a simple protocol for the cryopreservation of embryogenic suspension cultures of Cyclamen persicum. Embryogenic suspension cultures in the linear growth phase 7-10 days after subculture were used for cryopreservation. Of the different cryoprotectants tested during a 2-day pre-culture, 0.6 M sucrose resulted in the highest re-growth rates of 75%. An additional pre-treatment with 0.6 M sucrose and 10% DMSO (dimethylsulfoxide) for 1 h also positively affected re-growth. Microscopic studies on viability revealed that only few small embryogenic cells survived cryopreservation, while vacuolated single cells died. Experiments in which the duration of the pre-culture period - i.e. the length of time the embryogenic suspension cells were exposed to 0.6 M sucrose - was varied showed that 2-4 days was the most optimal exposure time to 0.6 M sucrose. Callus re-grown after cryopreservation showed growth rates similar to that of unfrozen callus and regenerated even higher numbers of somatic embryos than unfrozen callus.

Keywords

    Long-term storage, Pre-culture, Re-growth, Somatic embryogenesis

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Cryopreservation of embryogenic suspension cultures of Cyclamen persicum Mill. / Winkelmann, Traud; Mußmann, Viola; Serek, Margrethe.
In: Plant cell reports, Vol. 23, No. 1-2, 25.05.2004, p. 1-8.

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Winkelmann T, Mußmann V, Serek M. Cryopreservation of embryogenic suspension cultures of Cyclamen persicum Mill. Plant cell reports. 2004 May 25;23(1-2):1-8. doi: 10.1007/s00299-004-0783-1
Winkelmann, Traud ; Mußmann, Viola ; Serek, Margrethe. / Cryopreservation of embryogenic suspension cultures of Cyclamen persicum Mill. In: Plant cell reports. 2004 ; Vol. 23, No. 1-2. pp. 1-8.
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AU - Mußmann, Viola

AU - Serek, Margrethe

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