Mizuhiro M, Kenichi Y, Ito K, Kadowaki S, Ohashi H, Mii M
Plant Cell Technology Laboratory, Faculty of Horticulture, Chiba University, 648 Matsudo, Chiba 271-8510, Matsudo-City, Japan
Plant Sci. 2001 May;160(6):1221-1228. doi: 10.1016/s0168-9452(01)00390-9.
Protoplasts were isolated from cell suspension cultures of Primula malacoides cv. 'Lovely Tokyo' and P. obconica cv. 'Aalsmeer Giant White'. P. obconica protoplasts were embedded in 0.1% (w/v) gellan gum-solidified discs comprising MS medium supplemented with 3 mg/l of 2,4-D or picloram, 0.1 mg/l of zeatin, 0.2 M glucose and 0.2 M mannitol, and surrounded by a liquid medium of the same composition except for the addition of 0.1% (w/v) activated charcoal. The protoplasts formed visible colonies, which were transferred to the regeneration medium containing 30 g/l of sucrose, 0.1 mg/l of picloram and 2 mg/l of zeatin for shoot induction. P. malacoides protoplasts formed visible colonies when cultured in disc culture using 0.1% (w/v) gellan gum-solidified MS medium containing 5 mg/l of 2,4-D, 1 mg/l of NAA, 0.1 mg/l of zeatin and 0.4 M glucose. Small calli were transferred to MS medium supplemented with 5 mg/l of zeatin for shoot regeneration. The shoots of both species readily rooted on plant growth regulator-free 1/2 MS medium and successfully acclimatized to greenhouse conditions. The protoplast-derived plants showed some alterations in morphological characteristics from those of the in-vitro-germinated control plants.
从报春花品种‘可爱东京’和‘阿尔斯梅尔巨型白’的细胞悬浮培养物中分离原生质体。将小报春原生质体包埋在由添加了3mg/L 2,4 - D或毒莠定、0.1mg/L玉米素、0.2M葡萄糖和0.2M甘露醇的MS培养基组成的0.1%(w/v)结冷胶固化圆片中,并被除添加了0.1%(w/v)活性炭外的相同组成的液体培养基包围。原生质体形成可见菌落,将其转移至含有30g/L蔗糖、0.1mg/L毒莠定和2mg/L玉米素的再生培养基中诱导芽的形成。当在使用含有5mg/L 2,4 - D、1mg/L萘乙酸、0.1mg/L玉米素和0.4M葡萄糖的0.1%(w/v)结冷胶固化MS培养基的圆片培养中培养时,报春花‘可爱东京’原生质体形成可见菌落。将小愈伤组织转移至添加了5mg/L玉米素的MS培养基中进行芽再生。两个品种的芽都很容易在不含植物生长调节剂的1/2MS培养基上生根,并成功适应温室条件。原生质体再生植株与体外萌发的对照植株相比,在形态特征上表现出一些变化。