Abstract
Shoot tips of sweet potato were successfully cryopreserved using an encapsulation vitrification method. Encapsulated shoot tips were pre-incubated in liquid Murashige-Skoog medium containing 30 g/l sucrose for 24 h, then precultured in sucrose-enriched medium (0.3 M sucrose) for 16 h. Shoot tips were osmoprotected with a mixture of 2 M glycerol and 1.6 M sucrose for 3 h before being dehydrated with a highly concentrated vitrification solution (PVS2) for 1 h at 25°C. The encapsulated and dehydrated shoot tips were transferred to a 2 ml cryotube, suspended in 0.5 ml PVS2, and plunged directly into liquid nitrogen. Rapidly warmed shoot tips developed normal shoots and roots in 21 days without any morphological abnormalities after plating on a recovery medium. High levels (average of about 80%) of shoot formation were obtained for three cultivars of sweet potato. This encapsulation vitrification method appears promising for cryopreservation of sweet potato germplasm.
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Abbreviations
- BA :
-
6-Benzyl aminopurine
- DMSO :
-
Dimethyl sulfoxide
- GA 3 :
-
Gibberellic acid 3
- IAA :
-
Indole-3-acetic acid
- LN :
-
Liquid nitrogen
- MS :
-
Murashige-Skoog medium
- NAA :
-
1-Naphthaleneacetic acid
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Acknowledgement
The authors wish to thank Dr. Kei Shimonishi, Kagoshima Biotechnology Institute for supplying in-vitro-grown sweet potato plants
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Communicated by G.C. Phillips
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Hirai, D., Sakai, A. Simplified cryopreservation of sweet potato [Ipomoea batatas (L.) Lam.] by optimizing conditions for osmoprotection. Plant Cell Rep 21, 961–966 (2003). https://doi.org/10.1007/s00299-003-0618-5
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DOI: https://doi.org/10.1007/s00299-003-0618-5