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首页> 外文期刊>Plant Genetic Resources >Cryopreservation of in vitro-grown shoot tips of strawberry by the vitrification method using aluminium cryo-plates
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Cryopreservation of in vitro-grown shoot tips of strawberry by the vitrification method using aluminium cryo-plates

机译:铝制冷冻板通过玻璃化法冷冻保存草莓的离体芽梢

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摘要

Cryopreservation using an aluminium cryo-plate was successfully applied to in vitro-grown strawberry (Fragaria × ananassa Duch.) shoot tips. The shoots were cold-hardened at 5°C for 3 weeks with an 8-h photoperiod. The shoot tips (1.5–2.0 mm × 0.5–1.0 mm) were dissected from the shoot and pre-cultured at 5°C for 2 d on Murashige and Skoog medium containing 2 M glycerol and 0.3 M sucrose. The pre-cultured shoot tips were placed on the aluminium cryo-plate containing ten wells embedded in alginate gel. Osmoprotection was performed by immersing the cryo-plates in a loading solution (2 M glycerol and 0.8 M sucrose) for 30 min at 25°C. Dehydration was performed by immersing the cryo-plates in plant vitrification solution 2 for 50 min at 25°C. Then, the cryo-plate with shoot tips was transferred into an uncapped cryotube that was held on a cryo-cane and directly immersed into liquid nitrogen (LN). After storage in LN, shoot tips attached to the cryo-plate were directly immersed into 2 ml of a 1 M sucrose solution for regeneration. Using this procedure, the average regrowth level of vitrified shoot tips of 15 strawberry cultivars reached 81%. This new method has many advantages and will facilitate the cryostorage of strawberry germplasm.
机译:使用铝制低温板的低温保存已成功应用于体外生长的草莓(Fragaria×ananassa Duch。)枝梢。将芽用8小时的光周期在5℃下冷硬化3周。从茎上切下茎尖(1.5–2.0 mm×0.5–1.0 mm),并在5°C下在含有2 M甘油和0.3 M蔗糖的Murashige和Skoog培养基上预培养2 d。将预培养的芽尖放置在铝制冰冻板上,该冰冻板包含十个嵌入藻酸盐凝胶中的孔。通过将冷冻板在25℃下浸入加载溶液(2 M甘油和0.8 M蔗糖)中30分钟来进行渗透保护。通过将冷冻板在25℃下浸入植物玻璃化溶液2中50分钟来进行脱水。然后,将带有芽尖的冷冻板转移到未封盖的冷冻管中,将其固定在冷冻棒上并直接浸入液氮(LN)中。在LN中储存后,将附着在冷冻板上的芽尖直接浸入2 ml的1 M蔗糖溶液中进行再生。使用此程序,15个草莓品种的玻璃化芽尖端的平均再生水平达到81%。这种新方法具有许多优点,并且将有助于草莓种质的低温贮藏。

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