Hu Wei Hsin, Yang Yue Han, Liaw Song Iuan, Chang Chen
Department of Biology, National Museum of Natural Science, Taichung, 404, Taiwan.
Department of Horticulture, National Chung Hsing University, Taichung, 402, Taiwan.
Bot Stud. 2013 Dec;54(1):33. doi: 10.1186/1999-3110-54-33. Epub 2013 Sep 12.
The cryopreservation of orchid seeds is an important conservation method, studies of the effects of cryopreservation on the seeds of wild orchids are scant. This investigation was to establish a method for the vitrification and cryopreservation of seeds of B. formosana that may be suitable for the long term storage of Taiwan native orchid germplasm for conservation purposes.
The germination rate and morphological stability of seeds from spontaneous-dehiscent capsules of Bletilla formosana (Hayata) Schltr. were evaluated after cryopreservation by vitrification. The germination rates of cryopreserved seeds varied according to immersion time and the vitrification method used. Seeds that were dehydrated by immersion in loading solution (LS; 2.0 M glycerol, 0.4 M sucrose) for 10 min to 30 min then transferred to plant vitrification solution 2 (PVS2) for 30 min prior to freezing in liquid nitrogen (LN) showed significantly higher germination rates than seeds immersed in PVS2 only. The optimal immersion times were 10 min for LS and 30 min for PVS2, resulting in an in vitro germination rate of 91%. Germination was not observed for cryopreserved seeds that were dehydrated by immersion in LS only. Seed viabilities and germination rates did not vary significantly for cryostorage times from 10 minutes to 1 year.
This study improve, an efficient protocol was established that maintained seed viability and enhanced the germination rates of seeds, compared with previously described cryopreservation methods, and the germinated seeds showed normal morphology of both vegetative and reproductive organs.
兰花种子的冷冻保存是一种重要的保护方法,但关于冷冻保存对野生兰花种子影响的研究较少。本研究旨在建立一种适合台湾本土兰花种质长期保存的台湾白及种子玻璃化冷冻保存方法。
对台湾白及自然开裂蒴果的种子进行玻璃化冷冻保存后,评估其发芽率和形态稳定性。冷冻保存种子的发芽率因浸泡时间和所用玻璃化方法而异。将种子浸入装载溶液(LS;2.0 M甘油,0.4 M蔗糖)中脱水10分钟至30分钟,然后在液氮(LN)中冷冻前转移至植物玻璃化溶液2(PVS2)中30分钟,其发芽率显著高于仅浸入PVS2的种子。最佳浸泡时间为LS 10分钟,PVS2 30分钟,体外发芽率为91%。仅浸入LS脱水的冷冻保存种子未观察到发芽。冷冻保存10分钟至1年的种子活力和发芽率无显著差异。
本研究改进了方法,建立了一个有效的方案,与先前描述的冷冻保存方法相比,该方案保持了种子活力并提高了种子发芽率,且发芽种子的营养器官和生殖器官形态正常。