Takagi H, Tien Thinh N, Islam O M, Senboku T, Sakai A
Japan International Research Center for Agricultural Sciences, Okinawa Subtropical Station, 1091-1 Kawarabaru, Maesato, Ishigaki city, 907, Okinawa, Japan.
, Asabucho 1-5-23, Kitaku, 001, Sapporo, Japan.
Plant Cell Rep. 1997 Jun;16(9):594-599. doi: 10.1007/BF01275498.
Invitro-grown shoot tips of taro (Colocasia esculenta (L.) Schott.) were successfully cryopreserved by vitrification. Excised shoot tips precultured on solidified MS supplemented with 0.3M sucrose and maintained under a 16 h phtoperiod at 25°C for 16 h were loaded with a mixture of 2M glycerol plus 0.4M sucrose for 20 min at 25°C. The shoot tips were then sufficiently dehydrated with a highly concentrated vitrification solution (PVS2) for 20 min at 25°C prior to immersion into liquid nitrogen. Successfully vitrified and warmed shoot tips resumed growth within 7 days and developed shoots directly without intermediate callus formation. The average rate of shoot recovery amounted to around 80%, and the vitrification protocol appeared to be very promising for the cryopreservation of taro germplasm.
通过玻璃化法成功对离体培养的芋头(Colocasia esculenta (L.) Schott.)茎尖进行了超低温保存。将切下的茎尖在添加了0.3M蔗糖的固化MS培养基上预培养,并在25°C、16小时光周期条件下保持16小时,然后在25°C用2M甘油加0.4M蔗糖的混合物处理20分钟。接着在25°C用高浓度玻璃化溶液(PVS2)将茎尖充分脱水20分钟,之后浸入液氮。成功玻璃化并解冻的茎尖在7天内恢复生长,直接形成芽,无中间愈伤组织形成。芽的平均恢复率约为80%,该玻璃化方案对于芋头种质的超低温保存似乎非常有前景。