Department of Horticultural Plants Genetics and Breeding, Warsaw Agricultural University, Nowoursynowska 166, PL-02766, Warszawa, Poland.
Plant Cell Rep. 1985 Oct;4(5):269-73. doi: 10.1007/BF00269375.
A method for leaf mesophyll protoplast isolation and plant regeneration of cucumber (Cucumis sativus L.) is described. Using an isolation solution complemented with 0.1 M glycine, 8.2·10(6) viable protoplasts were isolated from 1 g of fresh leaves. The effect of the growth substances indole-3-acetic acid, naphthalene acetic acid, 2,4,-dichlorophenoxy acetic acid, 6-benzylaminopurine, 2-isopentenyladenine and kinetin at concentrations from 0.5 to 5 mg·1(-1) was studied using the multi-hanging drop technique. The optimal growth substance combination, namely 5 mg·1(-1) naphthalene acetic acid and 3 mg·1(-1) 2-isopentenyladenine, together with agarose medium in a so-called bead culture resulted in a plating efficiency of 21%. Some of the colonies obtained regenerated to plantlets which developed to plants.
描述了一种黄瓜(Cucumis sativus L.)叶片叶肉原生质体分离和植株再生的方法。使用含有 0.1 M 甘氨酸的分离溶液,从 1 g 新鲜叶片中分离出 8.2·10(6)个活原生质体。使用多悬滴技术研究了浓度为 0.5 至 5 mg·1(-1)的吲哚-3-乙酸、萘乙酸、2,4,-二氯苯氧乙酸、6-苄基氨基嘌呤、2-异戊烯腺嘌呤和激动素等生长物质的影响。最佳生长物质组合,即 5 mg·1(-1)萘乙酸和 3 mg·1(-1)2-异戊烯腺嘌呤,与琼脂糖培养基一起在所谓的珠粒培养中导致平板效率为 21%。获得的一些菌落再生为幼苗,这些幼苗发育成植物。