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首页> 外文期刊>Plant Cell, Tissue and Organ Culture: An International Journal on in Vitro Culture of Higher Plants >High-efficiency vitrification protocols for cryopreservation of in vitro grown shoot tips of transgenic papaya lines
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High-efficiency vitrification protocols for cryopreservation of in vitro grown shoot tips of transgenic papaya lines

机译:高效玻璃化协议,用于冷冻保存转基因木瓜品系的体外生长梢

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摘要

In vitro grown shoot tips of transgenic papaya lines (Carica papaya L.) were successfully cryopreserved by vitrification. Shoot tips were excised from stock shoots that were preconditioned in vitro for 45-50-day-old and placed on hormone-free MS medium with 0.09 M sucrose. After loading for 60 min with a mixture of 2 M glycerol and 0.4 M sucrose at 25pC, shoot tips were dehydrated with a highly concentrated vitrification solution (PVS2) for 80 min at 0pC and plunged directly into liquid nitrogen. The regeneration rate was approximately 90% after 2 months post-thawing. Successfully vitrified and warmed shoot tips of three non-transgenic varieties and 13 transgenic lines resumed growth within 2 months and developed shoots in the absence of intermediate callus formation. Dehydration with PVS2 was important for the cryopreservation of transgenic papaya lines. This vitrification procedure for cryopreservation appears to be promising as a routine method for cryopreserving shoot tips of transgenic papaya line germplasm.
机译:通过玻璃化成功冷冻保存了转基因木瓜品系(番木瓜L.)的体外生长梢。从茎中切下茎尖,将茎在体外预处理45-50天,并置于含有0.09 M蔗糖的无激素MS培养基上。在25pC下用2 M甘油和0.4 M蔗糖的混合物加载60分钟后,用高浓度的玻璃化溶液(PVS2)在0pC下将茎尖脱水80分钟,然后直接浸入液氮中。解冻后2个月,再生率约为90%。成功地玻璃化和加热了三个非转基因品种和13个转基因品系的芽尖,在两个月内恢复了生长,并且在没有中间愈伤组织形成的情况下形成了芽。 PVS2脱水对于转基因木瓜品系的冷冻保存很重要。这种用于冷冻保存的玻璃化方法有望作为一种常规方法用于冷冻保存转基因木瓜品系种芽梢。

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