Suppr超能文献

三种基于玻璃化的冷冻保存程序对马铃薯茎尖造成不同的冷冻损伤,而所有程序都能在再生植株中保持遗传完整性。

Three vitrification-based cryopreservation procedures cause different cryo-injuries to potato shoot tips while all maintain genetic integrity in regenerants.

作者信息

Wang Biao, Li Jing-Wei, Zhang Zhi-Bo, Wang Ren-Rui, Ma Yan-Li, Blystad Dag-Ragnar, Keller E R Joachim, Wang Qiao-Chun

机构信息

State Key Laboratory of Crop Stress Biology in Arid Areas, Key Laboratory of Genetic Improvement of Horticultural Crops of Northwest China of Ministry of Agriculture of China, College of Horticulture, Northwest A&F University, Yangling 712100 Shaanxi, PR China.

State Key Laboratory of Crop Stress Biology in Arid Areas, Key Laboratory of Genetic Improvement of Horticultural Crops of Northwest China of Ministry of Agriculture of China, College of Horticulture, Northwest A&F University, Yangling 712100 Shaanxi, PR China; Plant Health and Plant Protection Division, Bioforsk, N-4213 Ås, Norway.

出版信息

J Biotechnol. 2014 Aug 20;184:47-55. doi: 10.1016/j.jbiotec.2014.04.021. Epub 2014 May 22.

Abstract

We previously reported successful cryopreservation of shoot tips of potato 'Zihuabai' by three vitrification-based protocols. In the present study, cryo-injury to shoot tips and genetic stability in regenerants recovered from cryopreserved shoot tips by the three vitrification-based protocols were further investigated. The results showed that sucrose preculture caused no obviously different injuries, while dehydration with plant vitrification solution 2 (PVS2) was the step causing major damage to cells of shoot tips, regardless of the cryogenic procedures. Compared with droplet-vitrification and encapsulation-vitrification, vitrification caused the most severe injury to cells of the shoot tips, thus resulting in much longer time duration for shoot recovery and much lower shoot regrowth rate. Cells in apical dome and the youngest leaf primordia were able to survive and subsequently some of them regrew into shoots following all three vitrification-based cryopreservation procedures. Analyses using inter-simple sequence repeat (ISSR) and amplified fragment length polymorphism (AFLP) markers in shoots regrown from all three vitrification-based protocols did not find any polymorphic bands. The results reported here suggest that vitrification-based cryo-procedures can be considered promising methods for long-term preservation of potato genetic resources.

摘要

我们之前报道过通过三种基于玻璃化法的方案成功对马铃薯‘紫花白’茎尖进行超低温保存。在本研究中,进一步研究了这三种基于玻璃化法的方案对茎尖的冷冻损伤以及从冷冻保存的茎尖再生植株的遗传稳定性。结果表明,蔗糖预培养造成的损伤无明显差异,而使用植物玻璃化溶液2(PVS2)脱水是对茎尖细胞造成主要损伤的步骤,与冷冻程序无关。与滴冻玻璃化法和包埋玻璃化法相比,玻璃化法对茎尖细胞造成的损伤最严重,从而导致茎尖恢复所需时间更长,茎尖再生率更低。在所有三种基于玻璃化法的超低温保存程序后,顶端分生组织和最幼叶原基中的细胞能够存活,随后其中一些细胞再生为茎尖。使用简单序列重复区间(ISSR)和扩增片段长度多态性(AFLP)标记对所有三种基于玻璃化法的方案再生的茎尖进行分析,未发现任何多态性条带。此处报道的结果表明,基于玻璃化法的冷冻程序可被视为长期保存马铃薯遗传资源的有前景的方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验