Maize Mitochondria: Purification and Characterization of Ribosomes and Ribosomal Ribonucleic Acid
Author(s) -
D. R. Pring
Publication year - 1974
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.53.5.677
Subject(s) - ribosome , ribosomal rna , mitochondrial ribosome , biochemistry , rna , differential centrifugation , cytoplasm , ribosomal protein , 5s ribosomal rna , sucrose , biology , mitochondrion , centrifugation , denaturation (fissile materials) , microbiology and biotechnology , polyacrylamide gel electrophoresis , chemistry , gene , nuclear chemistry , enzyme
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.
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