Thimann Laboratories, University of California, Santa Cruz, California 95064.
Plant Physiol. 1978 Jul;62(1):40-3. doi: 10.1104/pp.62.1.40.
Protoplasts were prepared from castor bean (Ricinus communis) endosperm by treatment with a mixture of the commercial enzymes Macerozyme R-10 and Cellulose "Onozuka" R-10. The protoplasts were gently ruptured by forcing the suspension through a hypodermic needle and the homogenate centrifuged on a linear sucrose gradient. From such a homogenate the mitochondria are recovered at their typical isopycnic density of 1.18 g/ml, but the glyoxysomes are retained, with other membranes, at a density of 1.13. The plastids reach their typical density of 1.22 on the gradient and are thus clearly separated from other organelles. Moreover, since essentially all of the ribulose bisphosphate carboxylase activity on the gradient is present in this fraction it can be concluded that the plastids are intact and have been recovered in high yield.
原生质体通过用商业酶 Macerozyme R-10 和纤维素“Onozuka”R-10 的混合物处理蓖麻(Ricinus communis)胚乳来制备。将悬浮液通过皮下注射针轻轻破裂原生质体,然后将匀浆在蔗糖线性梯度上离心。从这样的匀浆中,线粒体在其典型的等密度 1.18 g/ml 处回收,但乙醛酸体与其他膜一起保留在密度为 1.13 的位置。质体在梯度上达到其典型密度 1.22,因此与其他细胞器明显分离。此外,由于梯度上基本上所有的核酮糖二磷酸羧化酶活性都存在于该部分中,可以得出结论,质体是完整的并且以高产率回收。