Cryopreservation of Cyrtopodium hatschbachii Pabst (Orchidaceae) immature seeds by encapsulation-dehydration.

M. Surenciski, E. Flachsland, G. Terada, L. Mroginski, H. Rey
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引用次数: 18

Abstract

The aim of the present study was to investigate the efficiency of the encapsulation-dehydration technique for cryopreservation of Cyrtopodium hastchbachii Pabst seeds. Immature seeds of this species were cryopreserved by an encapsulation-dehydration technique. Seeds of five immature pods, 120 days after pollination, were encapsulated in 3% calcium alginate matrix and pretreated in liquid medium supplemented with 0.08 M sucrose (24 h), 0.15 M sucrose (24 h), 0.25 M sucrose (48 h), 0.5 M sucrose (24 h) and 0.75 M sucrose (24 h) in shaker at 60 rpm. Alginate beads were dehydrated 5 h in silicagel and immersed in liquid nitrogen for 12 h. Cryopreserved beads were thawed at 30 degrees C for 1 min, rehydrated using the same liquid mediums [0.75 M sucrose (24 h), 0.5 M sucrose (24 h), 0.25 M sucrose (48 h) and 0.15 M sucrose (24 h)] and cultivated in half strength Murashige & Skoog medium (1962) with the addition of 2 g/L activated charcoal. Sixty four percent of seeds survived and developed into acclimatized plants after being cryopreserved. In this work, the encapsulation-dehydration technique was employed for first time in Cyrtopodium hatschbachii.
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包封脱水法低温保存兰科哈奇兰未成熟种子。
本研究的目的是研究包封-脱水技术在水杨桃种子冷冻保存中的效果。本种未成熟种子采用包封脱水技术冷冻保存。授粉120 d后,将5个未成熟荚果的种子包埋在3%海藻酸钙基质中,分别在添加0.08 M蔗糖(24 h)、0.15 M蔗糖(24 h)、0.25 M蔗糖(48 h)、0.5 M蔗糖(24 h)和0.75 M蔗糖(24 h)的液体培养基中进行预处理,摇床转速为60 rpm。海藻酸盐微球在硅胶中脱水5小时,在液氮中浸泡12小时。冷冻保存的微球在30℃下解冻1分钟,使用相同的液体培养基[0.75 M蔗糖(24小时),0.5 M蔗糖(24小时),0.25 M蔗糖(48小时)和0.15 M蔗糖(24小时)]再水化,并在半强度Murashige & Skoog培养基(1962)中培养,添加2g /L活性炭。64%的种子在冷冻保存后存活并发育成适应环境的植物。本研究首次采用包封脱水技术对哈氏细胞株进行了研究。
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