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基因工程改造的海藻糖积累提高了菊花(菊属大花菊品种)茎尖的冷冻保存耐受性。

Geneticallly enginereed trehalose accumulation improves cryopreservation tolerance of chrysanthemum (Dendranthema grandiflorum kitam.) shoot-tips.

作者信息

Osorio-Saenz Antelmo, Oscar Mascorro-Gallardo Jose, del Rocío Valle-Sandoval María, Teresa González-Arnao María, Engelmann Florent

机构信息

Universidad Autónoma Chapingo, Departamento de Fitotecnia, Chapingo Estado, México.

出版信息

Cryo Letters. 2011 Nov-Dec;32(6):477-86.

Abstract

Shoot-tips isolated from two transgenic lines of chrysanthemum (Dendranthema grandiflorum Kitam.) var. Indianapolis in vitro plantlets with induced capacity to biosynthesize trehalose, and from a non-transformed line, were subjected to cryopreservation using a vitrification procedure. After dissection, apices were precultured on semi-solid MS medium with 0.3 M sucrose for 4 days, loaded in a 0.4 M sucrose + 2 M glycerol solution for 20-30 min and exposed to PVS2 or PVS3 vitrification solutions for 0, 20, 40 or 60 min at room temperature prior to rapid immersion in liquid nitrogen. The highest shoot regeneration after cryopreservation was obtained with exposure to either PVS solution for 40 min. Plant regeneration from cryopreserved shoot-tips ranged between 48 percent and 67 percent for transgenic lines and between 33 percent and 36 percent for non-transgenic lines. No polymorphic loci were detected in plantlets regenerated from cryopreserved and non-cryopreserved shoot-tips with RAPD techniques using eight primers that amplified 101 monomorphic loci.

摘要

从两个具有诱导合成海藻糖能力的转基因菊花(Dendranthema grandiflorum Kitam.)品种印第安纳波利斯的离体苗以及一个未转化品系中分离出茎尖,采用玻璃化法进行超低温保存。解剖后,将茎尖在含有0.3 M蔗糖的半固体MS培养基上预培养4天,然后在0.4 M蔗糖 + 2 M甘油溶液中装载20 - 30分钟,并在室温下于PVS2或PVS3玻璃化溶液中分别处理0、20、40或60分钟,随后迅速浸入液氮。超低温保存后,经40分钟PVS溶液处理获得的茎尖再生率最高。转基因品系经超低温保存的茎尖再生植株率在48%至67%之间,未转基因品系则在33%至36%之间。使用8种引物对经超低温保存和未超低温保存的茎尖再生的植株进行RAPD分析,共扩增出101个单态位点,未检测到多态性位点。

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