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采用玻璃化法对离体甜菜(Beta vulgaris L.)茎尖进行超低温保存

Cryopreservation of in vitro sugar beet (Beta vulgaris L.) shoot tips by a vitrification technique.

作者信息

Vandenbussche B, Weyens G, De Proft M

机构信息

Laboratory of Plant Culture, Catholic University of Leuven, Willem de Croylaan 42, 3001 Heverlee, Belgium e-mail:

ADVANTA, Industriepark Soldatenplein Z2 15, 3300 Tienen, Belgium, , , , , , BE.

出版信息

Plant Cell Rep. 2000 Nov;19(11):1064-1068. doi: 10.1007/s002990000232.

Abstract

Sugar beet shoot tips from cold-acclimated plants were successfully cryopreserved using a vitrification technique. Dissected shoot tips were precultured for 1 day at 5  °C on solidified DGJ0 medium with 0.3 M sucrose. After loading for 20 min with a mixture of 2 M glycerol and 0.4 M sucrose (20  °C), shoot tips were dehydrated with PVS2 (0  °C) for 20 min prior to immersion in liquid nitrogen. Both cold acclimation and loading enhanced the dehydration tolerance of shoot tips to PVS2. After thawing, shoot tips were deloaded for 15 min in liquid DGJ0 medium with 1.2 M sucrose (20  °C). The optimal exposure time to both loading solution and PVS2 depended on the in vitro morphology of the clone. With tetraploid clones a higher sucrose concentration during cold acclimation and preculture further enhanced survival after cryopreservation. Survival rates ranged between 60% and 100% depending on the clone. Since only 10-50% of the surviving shoot tips developed into non-hyperhydric shoots, regrowth was optimized.

摘要

利用玻璃化技术成功地对冷驯化植株的甜菜茎尖进行了超低温保存。将切下的茎尖在含有0.3M蔗糖的固化DGJ0培养基上于5℃预培养1天。用2M甘油和0.4M蔗糖的混合物(20℃)装载20分钟后,茎尖在PVS2(0℃)中脱水20分钟,然后浸入液氮中。冷驯化和装载均增强了茎尖对PVS2的脱水耐受性。解冻后,茎尖在含有1.2M蔗糖的液态DGJ0培养基(20℃)中卸载15分钟。对装载溶液和PVS2的最佳暴露时间取决于克隆的离体形态。对于四倍体克隆,冷驯化和预培养期间较高的蔗糖浓度进一步提高了超低温保存后的存活率。存活率因克隆而异,介于60%至100%之间。由于只有10%-50%存活的茎尖发育成非玻璃化苗,因此对再生进行了优化。

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