Phenylalanyl-tRNA synthetases from yeast cytoplasm and mitochondria. The presence of a carbohydrate moiety in the mitochondrial enzyme and immunological evidence for structural relationship

Biochim Biophys Acta. 1983 Mar 30;743(3):451-4. doi: 10.1016/0167-4838(83)90405-3.

Abstract

Homogeneous yeast cytoplasmic and mitochondrial phenylalanyl-tRNA synthetases (L-phenylalanine:tRNAPhe ligase (AMP-forming), EC 6.1.1.20) are analysed for structural differences. Only the large subunit of the mitochondrial enzyme is a glycoprotein with nearly 3% carbohydrate by weight. The carbohydrates present are: glucose, N-acetylglucosamine, mannose, galactose and N-acetylneuraminic acid. Removal of the sugar moieties yields an activity increase, but no significant change of sensitivity to proteolytic degradation. Antibodies to both homogeneous enzymes demonstrate a structural similarity for both types of subunit using the highly sensitive immunoblotting technique.

Publication types

  • Comparative Study

MeSH terms

  • Amino Acyl-tRNA Synthetases / isolation & purification*
  • Antigen-Antibody Complex
  • Carbohydrates / analysis
  • Cytoplasm / enzymology
  • Epitopes / analysis
  • Immunodiffusion
  • Immunoelectrophoresis
  • Immunoglobulin G
  • Macromolecular Substances
  • Mitochondria / enzymology*
  • Phenylalanine-tRNA Ligase / isolation & purification*
  • Saccharomyces cerevisiae / enzymology*

Substances

  • Antigen-Antibody Complex
  • Carbohydrates
  • Epitopes
  • Immunoglobulin G
  • Macromolecular Substances
  • Amino Acyl-tRNA Synthetases
  • Phenylalanine-tRNA Ligase