E.N.I.T.H.P., Lab. Amélior. Plantes et Biotechnologies, 2 rue Le Nôtre, France.
Plant Cell Rep. 1993 Jan;12(2):118-20. doi: 10.1007/BF00241946.
Highly viable protoplasts were isolated in large numbers from in vitro-grown leaf and stem tissues of a haploid clone of the apple scion cultivar Golden Delicious (Malus Xdomestica Borkh.). Protoplasts from both sources divided rapidly to give microcallus, when cultured in a modified Kao and Michayluk-based medium. Following two successive subcultures for callusing, shoot buds were regenerated from such calli, on half-strength Murashige and Skoog medium with an increased concentration of group B vitamins and containing 5.0 mg.l(-1) 6-benzyl-aminopurine and 0.1 mg.l(-1) l-naphthaleneacetic acid (for the leaf protoplast-derived calli) or 4-indole-3yl-butyric acid (for stem protoplast-derived calli). The mesophyll protoplast-derived shoots were enfeebled and vitrified, in time with their ultimate death. Conversely, for those shoots deriving from the stem protoplasts, in vitro propagation was successfully achieved. This is the first report on the successful isolation, culture and organogenesis from stem protoplasts of a woody plant genotype.
从苹果品种金冠(Malus Xdomestica Borkh.)的单倍体无性系离体叶片和茎组织中大量分离出高活力原生质体。在改良的 Kao 和 Michayluk 基础培养基中培养时,两种来源的原生质体均迅速分裂形成微愈伤组织。继两次继代培养形成愈伤组织后,从这些愈伤组织在含有增加浓度的 B 族维生素的半强度 Murashige 和 Skoog 培养基上,以及含有 5.0mg.l(-1) 6-苄基氨基嘌呤和 0.1mg.l(-1) l-萘乙酸(用于叶片原生质体衍生的愈伤组织)或 4-吲哚-3-丁酸(用于茎原生质体衍生的愈伤组织)的条件下再生芽。随着最终死亡,叶片原生质体衍生的芽变得虚弱和玻璃化。相反,对于那些来自茎原生质体的芽,体外繁殖成功实现。这是关于木本植物基因型茎原生质体成功分离、培养和器官发生的首次报道。