Gupta Sandhya, Reed Barbara M
Tissue Culture and Cryopreservation Unit, National Bureau of Plant Genetic Resources, Pusa Campus, New Delhi, India.
Cryo Letters. 2006 Jan-Feb;27(1):29-42.
Encapsulation-dehydration and PVS2-vitrification cryopreservation protocols were evaluated for the long-term conservation of a diverse group of Rubus germplasm. Cold acclimation for a 4-week period prior to cryopreservation was necessary for regrowth of shoot apices from blackberry and raspberry genotypes. For the encapsulation-dehydration protocol, encapsulated apices were pretreated in 0.75 M sucrose for 20 h, desiccated 6-h under laminar flow to c. 20 percent moisture content, then plunged in liquid nitrogen (LN) and rapidly warmed. The PVS2-vitrification protocol included pretreating shoot tips on 5 percent dimethyl sulfoxide (DMSO) medium for 48 h, exposure to loading solution (LS) and PVS2 for 20 min each at 25 degree C , followed by immersion in LN and rapid warming. Shoot tips of 25 genotypes in 9 Rubus species and 9 Rubus hybrids were successfully cryopreserved with recovery of 60 to 100 percent using the encapsulation-dehydration protocol. Four genotypes of 3 species were tested using the vitrification protocol with 71 percent average regrowth. The present results indicate that both of these improved cryopreservation protocols can be applied to a diverse range of Rubus genetic resources.
对包埋脱水法和PVS2玻璃化冷冻保存方案进行了评估,以长期保存多种悬钩子属种质资源。对于黑莓和树莓基因型的茎尖再生而言,在冷冻保存前进行为期4周的冷驯化是必要的。对于包埋脱水方案,将包埋的茎尖在0.75M蔗糖中预处理20小时,在层流条件下干燥6小时至含水量约20%,然后投入液氮并快速解冻。PVS2玻璃化方案包括在5%二甲基亚砜(DMSO)培养基上对茎尖预处理48小时,在25℃下分别在加载溶液(LS)和PVS2中处理20分钟,随后浸入液氮并快速解冻。使用包埋脱水方案成功冷冻保存了9种悬钩子属植物和9种悬钩子属杂种中的25个基因型的茎尖,恢复率为60%至100%。使用玻璃化方案对3个物种的4个基因型进行了测试,平均再生率为71%。目前的结果表明,这两种改进的冷冻保存方案均可应用于多种悬钩子属遗传资源。