Successful cryopreservation of suspension cells by encapsulation-dehydration
Identifieur interne : 003550 ( Main/Exploration ); précédent : 003549; suivant : 003551Successful cryopreservation of suspension cells by encapsulation-dehydration
Auteurs : Y. Bachiri [France] ; C. Gazeau [France] ; J. Hansz [France] ; C. Morisset [France] ; J. Dereuddre [France]Source :
- Plant Cell, Tissue and Organ Culture [ 0167-6857 ] ; 1995-12-01.
Abstract
Abstract: Cryopreservation of a Catharanthus cell suspension was performed after encapsulation in alginate beads. Encapsulated cells were precultured in sucrose-enriched medium for several days, dried over silica gel, and directly cooled in liquid nitrogen. After rewarming in air at room temperature, alginate beads were placed on semi-solid culture medium. Following regrowth, beads transferred to liquid medium generated a new cell suspension. Cell survival and regrowth from cryopreserved encapsulated cells depended on preculture duration and residual water content after air-drying.
Url:
DOI: 10.1007/BF00039951
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Abstract: Cryopreservation of a Catharanthus cell suspension was performed after encapsulation in alginate beads. Encapsulated cells were precultured in sucrose-enriched medium for several days, dried over silica gel, and directly cooled in liquid nitrogen. After rewarming in air at room temperature, alginate beads were placed on semi-solid culture medium. Following regrowth, beads transferred to liquid medium generated a new cell suspension. Cell survival and regrowth from cryopreserved encapsulated cells depended on preculture duration and residual water content after air-drying.</div>
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