Pure and Applied Biochemistry, University of Lund, Chemical Center, P.O. Box 740, S-22007, Lund, Sweden.
Plant Cell Rep. 1985 Feb;4(1):23-7. doi: 10.1007/BF00285497.
Protoplasts of Daucus carota Ca68 and Catharanthus roseus have been immobilized by entrapment in gelforming polysaccharides (kappa-carrageenan, agarose and alginate). Uniform spherical beads of carrageenan and agarose containing the protoplasts have been prepared by utilizing an inert hydrophobic phase (vegetable oil). The entrapped protoplasts are viable and stabilized towards osmotic shock by the polymeric backbone. Standard methods have been used to study the viability and integrity of the entrapped protoplasts. Upon incubation in a relatively simple medium the immobilized protoplasts show a much higher viability after 14 days as compared to free protoplasts under the same conditions. The viability of D. carota protoplasts has also been monitored by an enzyme activity present in the cells (digitoxigenin 58-hydroxylase).
胡萝卜 Ca68 和长春花原生质体已通过包埋在凝胶形成多糖(角叉菜胶、琼脂糖和海藻酸钠)中固定化。通过利用惰性疏油相(植物油)制备了含有原生质体的均匀球形卡拉胶和琼脂糖珠。聚合物主链使包埋的原生质体具有活力并稳定对抗渗透压冲击。已经使用标准方法研究了包埋原生质体的活力和完整性。在相对简单的培养基中孵育时,与相同条件下的游离原生质体相比,固定化原生质体在 14 天后显示出更高的活力。通过存在于细胞中的酶活性(洋地黄毒苷 5β-羟化酶)监测胡萝卜原生质体的活力。