Hokkaido National Agricultural Experiment Station, Hitsujigaoka, 1, 004, Sapporo, Japan.
Plant Cell Rep. 1990 Oct;9(6):328-31. doi: 10.1007/BF00232862.
Dried axillary buds from plantlets of Asparagus lofficinalis L. grown in vitro were successfully cryopreserved. Single node segments (5mm in length) with axillary bud were taken from mature in vitro plantlets. The segments were precultured on solidfied Murashige-Skoog medium (1962) containing 0.7M sucrose at 25 °C in light for 2 days. Thereafter, these precultured segments were subjected to dehydration with silica gel at room temperature for 0 to 24 h. The axillary buds of precultured segments tolerated dehydration to about 14% water content(FW) with 50% lethality (LD50) and the threshold water content at which the dried buds remained alive after exposure to liquid nitrogen was 16.9%(LD50). The maximum rate of survival of cryopreserved buds was about 71% of untreated control. Surviving buds produced shoots and regenerated into plantlets. These results demonstrate the feasibility of cryopreserving dried axillary buds from in vitro plantlets.
离体培养的天门冬腋芽干体成功实现了冷冻保存。从成熟的离体植株上切取带有腋芽的单节段(长 5mm)。将这些节段预培养在含有 0.7M 蔗糖的固体 Murashige-Skoog 培养基(1962)上,25°C 光照下预培养 2 天。此后,将这些预培养的节段在室温下用硅胶进行脱水处理 0 至 24 小时。预培养节段的腋芽可耐受约 14%含水量(FW)的脱水处理,50%致死率(LD50),在液氮暴露后存活的芽的阈值含水量为 16.9%(LD50)。经冷冻保存的芽的最大存活率约为未经处理对照的 71%。存活的芽产生了芽,并再生为植株。这些结果表明,从离体培养的植株中冷冻保存干燥腋芽是可行的。