Malemnganba H, Ray B K, Bhattacharyya S, Deka P C
Department of Agricultural Biotechnology, Assam Agricultural, University, Jorha, India.
Indian J Exp Biol. 1996 Aug;34(8):802-5.
Embryos (80 days old) developed after selfing P. tankervilliae were cultured on Nitsch medium for protocorm development. Protocorms (70 days old) thus developed were encapsulated with alginate matrix. Ninety six per cent of freshly prepared encapsulated protocorms differentiated into shoots and roots when cultured on Nitsch medium. Storage of encapsulated protocorms in sealed petri plates or by embedding in liquid paraffin at 4 degrees C showed no reduction in their regeneration frequency up to 120 days when cultured on Nitsch medium. However, 90% of encapsulated protocorms stored at room temperature in empty petri plates differentiated within 35-40 days. Regeneration frequency of encapsulated protocorms was drastically reduced when stored in liquid paraffin at room temperature.
将互叶醉鱼草自交后发育的胚(80日龄)在Nitsch培养基上培养以促进原球茎发育。如此发育形成的原球茎(70日龄)用藻酸盐基质进行包埋。当在Nitsch培养基上培养时,96%新制备的包埋原球茎分化形成芽和根。将包埋原球茎储存在密封培养皿中或于4℃下嵌入液体石蜡中,当在Nitsch培养基上培养时,其再生频率在120天内均未降低。然而,90%在空培养皿中室温保存的包埋原球茎在35 - 40天内分化。当在室温下储存在液体石蜡中时,包埋原球茎的再生频率急剧降低。