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首页> 外文期刊>In Vitro Cellular and Development Biology. Plant: Journal of the Tissue Culture Association >Low-temperature preincubation enhances survival and regeneration of cryopreserved Saussurea involucrata callus.
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Low-temperature preincubation enhances survival and regeneration of cryopreserved Saussurea involucrata callus.

机译:低温预培养可提高冷冻保存的雪莲的愈伤组织的存活和再生能力。

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摘要

Saussurea involucrata Kar. et Kir. is one of the most well-known Chinese medicinal plants, and it is utilized for a variety of medical conditions. Due to the overexploitation of this endangered species, it is crucial to develop methods for both conservation and propagation. To address this issue, we have developed and optimized a simple and effective vitrification process for the cryopreservation of S. involucrata callus tissue. The optimized method consisted of a 3-d incubation period on medium containing 0.3 M sucrose, transfer to a plant vitrification solution (PVS2) containing 30% (v/v) glycerol, 15% (v/v) ethylene glycol, 15% (v/v) dimethylsulfoxide, and 0.4 M sucrose first at 60% PVS2 for 40 min, then at 100% PVS2 for 60 min, followed by immediate immersion and storage in liquid nitrogen. To thaw the tissue, tissues were rewarmed at 40 degrees C for 2 min. This method resulted in a survival rate of approximately 56% and a regrowth rate of approximately 40%. Survival and regrowth were significantly improved by the addition of a low-temperature preincubation step. Incubating the calli at 4 degrees C for 12 d prior to initiating the optimized cryopreservation protocol increased the survival rate of the tissue to 75%, increased the regrowth rate to 60%, and more than doubled the number of regenerated shoots per explant. Following cryopreservation, greater than 90% of the regenerated shoots formed complete plantlets, and 81% of the regenerated plantlets survived and grew vigorously under greenhouse conditions.
机译:雪莲。等基尔。是最著名的中草药之一,它被用于多种医疗条件。由于该濒危物种的过度开发,开发保护和繁殖方法至关重要。为了解决这个问题,我们已经开发和优化了一种简单有效的玻璃化工艺,用于低温培养小球藻愈伤组织。优化的方法包括在含有0.3 M蔗糖的培养基上进行3天孵育,然后转移至含有30%(v / v)甘油,15%(v / v)乙二醇,15%(v)的甘油的植物玻璃化溶液(PVS2)中。 v / v)二甲基亚砜和0.4 M蔗糖,首先在60%PVS2下40分钟,然后在100%PVS2下60分钟,然后立即浸入并储存在液氮中。为了解冻组织,将组织在40摄氏度下加热2分钟。此方法的存活率约为56%,再生率约为40%。通过添加低温预孵育步骤,存活率和再生长显着提高。在开始优化的冷冻保存方案之前,将愈伤组织在4摄氏度下孵育12天可将组织的存活率提高到75%,将再生率提高到60%,并使每个外植体的再生芽数增加一倍以上。冷冻保存后,超过90%的再生苗形成完整的幼苗,而81%的再生苗在温室条件下存活并生长旺盛。

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