Agricultural Research Service, United States Department of Agriculture, Florida-Antilles Area, Department of Plant Pathology, University of Florida, Gainesville, Florida 32611.
Plant Physiol. 1974 May;53(5):677-83. doi: 10.1104/pp.53.5.677.
Mitochondria were prepared from etiolated maize shoots (Zea mays L. var. McNair 508) by homogenization followed by differential centrifugation and equilibrium banding in discontinuous sucrose or Renografin-sucrose gradients. Mitochondria prepared by sucrose banding showed better physiological integrity than those prepared by renografin-sucrose banding, although both procedures yielded mitochondria that showed respiratory control and coupling of oxidation to phosphorylation of ADP. Mitochondria prepared by Renografin-sucrose banding were free of dectectable cytoplasmic ribosomal RNA, while sucrose banding resulted in a low level of contamination. Ribosomes isolated from mitochondria sedimented at about 78S, with subunits sedimenting at 60 and 44S. Using Escherichia coli ribosomal RNA as internal standards, the molecular weights of mitochondrial ribosomal RNAs were found to be 0.74 to 0.75 and 1.26 x 10(6) daltons by polyacrylamide gel electrophoresis, before or after denaturation in formaldehyde. Cytoplasmic ribosomal RNA molecular weights were 0.70 and 1.26 x 16(6) before denaturation, and 0.68 and 1.5 x 10(6) after denaturation, suggesting an unusual reaction of the heavy ribosomal RNA to formaldehyde.
线粒体由玉米黄化苗(Zea mays L. var. McNair 508)通过匀浆,然后进行差速离心和不连续蔗糖或泛影葡胺-蔗糖梯度平衡带分离来制备。蔗糖带分离制备的线粒体比泛影葡胺-蔗糖带分离制备的线粒体具有更好的生理完整性,尽管这两种方法都得到了具有呼吸控制和氧化磷酸化偶联的 ADP 的线粒体。用泛影葡胺-蔗糖带分离制备的线粒体没有可检测到的细胞质核糖体 RNA,而蔗糖带分离则会导致低水平的污染。从线粒体分离的核糖体在约 78S 处沉降,亚基在 60 和 44S 处沉降。使用大肠杆菌核糖体 RNA 作为内部标准,通过聚丙烯酰胺凝胶电泳发现线粒体核糖体 RNA 的分子量在甲醛变性前后分别为 0.74 至 0.75 和 1.26 x 10(6) 道尔顿。细胞质核糖体 RNA 的分子量在变性前分别为 0.70 和 1.26 x 16(6),变性后分别为 0.68 和 1.5 x 10(6),这表明重核糖体 RNA 对甲醛的反应异常。