Suppr超能文献

用于阿兰达布罗加蓝兰花原球茎(PLB)的PVS2液滴玻璃化冷冻保存技术的开发。

Development of a PVS2 droplet-vitrification cryopreservation technique for Aranda Broga Blue orchid protocorm-like bodies (PLBs).

作者信息

Ping K S, Poobathy R R, Zakaria R, Subramaniam S

机构信息

School of Biological Sciences, Universiti Sains Malaysia (USM), Penang, Malaysia.

出版信息

Cryo Letters. 2017 Jul/Aug;38(4):290-298.

Abstract

UNLABELLED

BACKGROUND: Conservation of commercially important ornamental plants is important to maintain its unique beauty to cater the market demands.

OBJECTIVE

The main objective is to develop an efficient cryopreservation technique for Aranda Broga Blue orchid PLBs using droplet-vitrification method.

MATERIALS AND METHODS

Several critical factors in cryopreservation were accessed such as preculture concentrations and durations, choice of vitrification solutions, two-step or three-step vitrification, growth recovery medium and PVS2 exposure duration.

RESULTS

The best growth regeneration percentage (5%) was obtained when 3-4mm PLBs were precultured in 0.2M sucrose for 3 days, followed by osmoprotection for 20 minutes, dehydration in PVS2 for 20 minutes at 0 degree C, LN storage, thawed and unloading for 20 minutes, and growth regeneration in VW10 medium. PLBs were found to be very sensitive to osmotic stress imposed by high molecular weight cryoprotectant such as sucrose and glycerol. Osmotic potential of growth recovery medium is one of the main factors that affect growth recovery in cryopreserved PLBs.

CONCLUSION

Current report showed possibilities in cryopreserving Aranda Broga Blue PLBs using droplet-vitrification technique. However, further improvement of growth recovery can be done by focussing on approaches that facilitate sufficient water removal from PLBs without causing severe osmotic injuries to the plant cells.

摘要

未标记

背景:保护具有商业重要性的观赏植物对于保持其独特美感以满足市场需求至关重要。

目的

主要目的是使用玻璃化法为阿兰达·布罗加蓝兰花原球茎开发一种高效的冷冻保存技术。

材料与方法

评估了冷冻保存中的几个关键因素,如预培养浓度和持续时间、玻璃化溶液的选择、两步或三步玻璃化、生长恢复培养基和PVS2暴露持续时间。

结果

当3 - 4毫米的原球茎在0.2M蔗糖中预培养3天,接着进行20分钟的渗透压保护,在0℃下于PVS2中脱水20分钟,液氮保存,解冻并卸载20分钟,然后在VW10培养基中进行生长再生时,获得了最佳生长再生率(5%)。发现原球茎对蔗糖和甘油等高分子量冷冻保护剂施加的渗透胁迫非常敏感。生长恢复培养基的渗透势是影响冷冻保存原球茎生长恢复的主要因素之一。

结论

当前报告显示了使用玻璃化法冷冻保存阿兰达·布罗加蓝原球茎的可能性。然而,通过关注有助于从原球茎中充分去除水分而又不会对植物细胞造成严重渗透损伤的方法,可以进一步提高生长恢复率。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验