Cryopreservation of embryogenic suspension cultures of Cyclamen persicum Mill

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OriginalspracheEnglisch
Seiten (von - bis)1-8
Seitenumfang8
FachzeitschriftPlant cell reports
Jahrgang23
Ausgabenummer1-2
PublikationsstatusVeröffentlicht - 25 Mai 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.

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Cryopreservation of embryogenic suspension cultures of Cyclamen persicum Mill. / Winkelmann, Traud; Mußmann, Viola; Serek, Margrethe.
in: Plant cell reports, Jahrgang 23, Nr. 1-2, 25.05.2004, S. 1-8.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Winkelmann T, Mußmann V, Serek M. Cryopreservation of embryogenic suspension cultures of Cyclamen persicum Mill. Plant cell reports. 2004 Mai 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 ; Jahrgang 23, Nr. 1-2. S. 1-8.
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AU - Mußmann, Viola

AU - Serek, Margrethe

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