Friedrich Miescher-Institut, P.O. Box 273, CH-4002, Basel, Switzerland.
Plant Cell Rep. 1983 Oct;2(5):244-7. doi: 10.1007/BF00269151.
Two novel techniques improve division and colony formation from protoplasts: 1) Plating in agarose stimulates colony formation of protoplasts from a wide range of species. Protoplasts from Nicotiana tabacum developed to colonies from lower initial population densities in agarose than in agar or liquid. Protoplasts from Hyoscyamus muticus which do not divide in agar divided and formed colonies in agarose at higher efficiencies than in liquid medium. 2) Culture of gel embedded protoplasts in large volumes of liquid medium on a gyrotatory shaker ('bead culture') further improved plating efficiencies in some species (e.g. Lycopersicon esculentum and Crepis capillaris) and enabled sustained proliferation of protoplasts which had not previously developed beyond the few cell colony stage (Brassica rapa and a mutator gene variety of Petunia hybrida). The combination of 'agarose plating' and 'bead culture' dramatically improved plating efficiencies of protoplasts in all species tested.
1)琼脂糖平板法刺激了来自广泛物种的原生质体的集落形成。与琼脂或液体相比,来自烟草的原生质体在琼脂糖中的低初始种群密度下发育为集落。在琼脂中不分裂的天仙子原生质体在琼脂糖中的分裂和集落形成效率高于液体培养基。2)在旋转摇床上用大量液体培养基培养包埋在凝胶中的原生质体(“珠培养”)进一步提高了某些物种(如番茄和毛茛)的平板效率,并使先前未能超过少数细胞集落阶段的原生质体持续增殖(油菜和矮牵牛的突变基因品种)。“琼脂糖平板法”和“珠培养法”的结合极大地提高了所有测试物种中原生质体的平板效率。