Department of Botany, University of Delhi, 110007, Delhi, India.
Plant Cell Rep. 1982 Oct;1(5):219-20. doi: 10.1007/BF00270240.
Young leaves of Solanum xanthocarpum from axenic shoot cultures released viable protoplasts when treated with appropriate enzymes. The protoplasts on culture in modified Murashige and Skoog (1962) medium supplemented with 2,4-dichlorophenoxy-acetic acid (0.5 mg/l), naphtha leneacetic acid (1 mg/l), kinetin (1 mg/l) and organic nutrients of KM (Kao and Michayluk 1975) regenerated to form callus tissue as a result of repeated divisions. Protoplast-derived calli differentiated into shoots on MS medium enriched with kinetin (0.5 mg/l) and rooting could be initiated by transferring the shoot-buds to basal medium.
无菌培养的酸浆幼叶经适当的酶处理后可释放出有活力的原生质体。在改良的 Murashige 和 Skoog(1962)培养基中培养原生质体,添加 2,4-二氯苯氧乙酸(0.5mg/L)、萘乙酸(1mg/L)、激动素(1mg/L)和 KM 的有机营养物质(Kao 和 Michayluk 1975),由于反复分裂,原生质体衍生的愈伤组织再生为愈伤组织。从原生质体衍生的愈伤组织在富含激动素(0.5mg/L)的 MS 培养基上分化为芽,通过将芽转移到基本培养基上可以启动生根。