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冷冻网片:一种简单的替代性冷冻保存方案。

Cryo-mesh: a simple alternative cryopreservation protocol.

作者信息

Funnekotter B, Bunn E, Mancera R L

机构信息

School of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Perth; Botanic Gardens and Parks Authority, West Perth, Australia.

Botanic Gardens and Parks Authority, Fraser Avenue, West Perth; School of Plant Biology, Faculty of Science, The University of Western Australia, Crawley, Australia.

出版信息

Cryo Letters. 2017 Mar/Apr;38(2):155-159.

Abstract

BACKGROUND

The continued development of new cryopreservation protocols has improved post-cryogenic success rates for a wide variety of plant species. Methods like the cryo-plate have proven beneficial in simplifying the cryopreservation procedure.

OBJECTIVE

This study assessed the practicality of a stainless steel mesh strip (cryo-mesh) for cryopreserving shoot tips from Anigozanthos viridis.

MATERIALS AND METHODS

Shoot tips of A. viridis (Kangaroo Paw) were precultured on 0.4 M sucrose medium for 48 h. Precultured shoot tips were coated in a 2% alginate solution and placed onto the cryo-mesh (a 25 x 7 mm, 0.4 mm aperture, 0.224 mm diameter wire stainless steel mesh strip). The alginate was set for 20 min in a loading solution containing 100 mM CaCl2, anchoring the shoot tips to the cryo-mesh. The cryo-mesh was then transferred to PVS2 on ice for 20, 30 or 40 min prior to plunging the cryo-mesh into liquid nitrogen. The cryo-mesh protocol was compared to the droplet-vitrification protocol.

RESULTS

A maximum of 83% post-cryogenic regeneration was achieved with the cryo-mesh when exposed to PVS2 for 30 min. No significant difference in post-cryogenic regeneration was observed between the cryo-mesh and droplet-vitrification protocols.

CONCLUSION

Anigozanthos viridis shoot tips were successfully cryopreserved utilising the new cryo-mesh. The cryo-mesh thus provides a simple and successful alternative for cryopreservation.

摘要

背景

新的冷冻保存方案的不断发展提高了多种植物物种的低温保存成功率。冷冻板等方法已被证明有助于简化冷冻保存程序。

目的

本研究评估了不锈钢网带(冷冻网)用于冷冻保存绿毛袋鼠爪茎尖的实用性。

材料与方法

将绿毛袋鼠爪的茎尖在0.4M蔗糖培养基上预培养48小时。将预培养的茎尖包裹在2%海藻酸钠溶液中,然后放置在冷冻网上(一条25×7毫米、孔径0.4毫米、钢丝直径0.224毫米的不锈钢网带)。海藻酸钠在含有100mM氯化钙的装载溶液中凝固20分钟,将茎尖固定在冷冻网上。然后将冷冻网转移到冰上的PVS2中20、30或40分钟,之后将冷冻网投入液氮中。将冷冻网方案与玻璃化滴冻方案进行比较。

结果

冷冻网在PVS2中处理30分钟时,低温保存后的再生率最高可达83%。冷冻网方案和玻璃化滴冻方案在低温保存后的再生方面未观察到显著差异。

结论

利用新型冷冻网成功冷冻保存了绿毛袋鼠爪的茎尖。因此,冷冻网为冷冻保存提供了一种简单且成功的替代方法。

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