Sharma Neelam, Sharma Bindu
Tissue Culture and Cryopreservation Unit, National Bureau of Plant Genetic Resources, Pusa Campus, New Delhi-110012, India.
Cryo Letters. 2003 May-Jun;24(3):181-90.
The cryopreservation of shoot tips of Picrorhiza kurroa Royle ex Benth (IC 266698), an endangered medicinal plant of India was investigated. Shoot tips (about 1 mm in length) excised from four-week-old proliferating shoot cultures were precultured on MS medium supplemented with various osmotica before dehydrating with PVS2 solution at 0 degrees C. The dehydrated shoot tips were directly immersed in LN2. Following cryopreservation, and after rapid rewarming at 45 degrees C, shoot tips were quickly washed with 1.2 M sucrose solution and then plated on solidified shoot culture medium. Shoot tips were successfully cryopreserved by vitrification, when they were precultured on medium supplemented with 5% DMSO at 4 degrees C for two days before dehydrating in PVS2 for 10-20 minutes at 0 degrees C. Average survival in terms of normal shoot formation after 4 wks of plating was about 20% without callus formation. Cold hardening of shoot cultures for four weeks at 4 degrees C significantly improved the survival and shoot regeneration of cryopreserved shoot tips to 70% and 35%, respectively.
对印度濒危药用植物胡黄连(IC 266698)茎尖的冷冻保存进行了研究。从四周龄增殖芽培养物上切取的茎尖(长度约1毫米),在0℃用PVS2溶液脱水前,先在添加了各种渗透压调节剂的MS培养基上进行预培养。脱水后的茎尖直接浸入液氮。冷冻保存后,在45℃快速复温后,茎尖迅速用1.2M蔗糖溶液洗涤,然后接种在固化的芽培养基上。当茎尖在4℃添加5%DMSO的培养基上预培养两天,然后在0℃用PVS2脱水10 - 20分钟时,通过玻璃化法成功实现了茎尖的冷冻保存。接种4周后,正常芽形成方面的平均存活率约为20%,且无愈伤组织形成。在4℃对芽培养物进行四周的低温锻炼显著提高了冷冻保存茎尖的存活率和芽再生率,分别达到70%和35%。