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Isolation of Plasma Membranes from Corn Roots by Sucrose Density Gradient Centrifugation

机译:蔗糖密度梯度离心法从玉米根中分离质膜

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An investigation was conducted into the isolation of plasma membrane vesicles from primary roots of corn (Zea mays L., WF9 × M14) by sucrose density gradient centrifugation. Identification of plasma membranes in cell fractions was by specific staining with the periodic-chromic-phosphotungstic acid procedure. Plasma membrane vesicles were rich in K+-stimulated ATPase activity at pH 6.5, and equilibrated in linear gradients of sucrose at a peak density of about 1.165 g/cc. It was necessary to remove mitochondria (equilibrium density of 1.18 g/cc) from the homogenate before density gradient centrifugation to minimize mitochondrial contamination of the plasma membrane fraction. Endoplasmic reticulum (NADH-cytochrome c reductase) and Golgi apparatus (latent IDPase) had equilibrium densities in sucrose of about 1.10 g/cc and 1.12 to 1.15 g/cc, respectively. A correlation (r = 0.975) was observed between K+-stimulated ATPase activity at pH 6.5 and the content of plasma membranes in various cell fractions. ATPase activity at pH 9 and cytochrome c oxidase activity were also correlated.A major peak of ATPase activity at pH 6.5 was observed at low density in Ficoll after nonequilibrium centrifugation in a combination Ficoll-sucrose gradient. Twenty to forty percent of the vesicles in this ATPase fraction stained positively for plasma membranes, and with equilibrium centrifugation the major portion of the ATPase activity shifted to densities in sucrose which were characteristic of plasma membranes. All major vesicular ATPase activities observed in Ficoll or sucrose contained substantial amounts of plasma membranes. For unknown reasons, mitochondria and plasma membranes equilibrated over a broader density range and at lower peak densities in sucrose as a result of equilibrium centrifugation through Ficoll.
机译:通过蔗糖密度梯度离心法从玉米(Zea mays L.,WF9×M14)的初生根中分离质膜囊泡。在细胞部分中质膜的鉴定是通过用定期变色的磷钨酸程序进行的特异性染色来进行的。质膜囊泡在pH 6.5时富含K + 刺激的ATPase活性,并在蔗糖的线性梯度中达到平衡,峰值密度约为1.165 g / cc。在密度梯度离心之前,有必要从匀浆中除去线粒体(平衡密度为1.18 g / cc),以最大程度地减少质膜部分的线粒体污染。内质网(NADH-细胞色素C还原酶)和高尔基体(潜在IDPase)在蔗糖中的平衡密度分别约为1.10 g / cc和1.12至1.15 g / cc。观察到在pH 6.5时K + 刺激的ATPase活性与不同细胞部分质膜含量之间的相关性(r = 0.975)。 Ficoll-蔗糖梯度联合非平衡离心后,在低密度下,在Ficoll中观察到pH值为6.5时ATPase活性的一个主要峰值是在低密度下在Ficoll中观察到的。该ATPase馏分中有20%至40%的囊泡对质膜呈阳性染色,并且通过平衡离心,ATPase活性的主要部分转移到了质膜特征的蔗糖密度中。在Ficoll或蔗糖中观察到的所有主要水泡ATPase活性均含有大量的质膜。由于不明原因,通过Ficoll进行平衡离心后,线粒体和质膜在更宽的密度范围内和较低的蔗糖峰密度下达到平衡。

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