Kinetic analysis of an E.coli phenylalanine-tRNA synthetase mutant

Nucleic Acids Res. 1988 Aug 11;16(15):7477-86. doi: 10.1093/nar/16.15.7477.

Abstract

A mutation in the pheS gene, encoding phenylalanyl-tRNA synthetase, in E. coli NP37 confers temperature-sensitivity on the organism. A five-fold increase in tRNA(phe) levels complements the mutation. Analysis of the kinetic properties of the mutant enzyme indicates that the KM is 20-fold higher than the wild-type and the dissociation constant of the tRNA(phe)-synthetase complex for the mutant is at least 10-fold higher. These results indicate that the mutation in E. coli NP37 directly affects the tRNA(phe) binding site on the cognate synthetase.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acyl-tRNA Synthetases / genetics*
  • Escherichia coli / genetics*
  • Genetic Complementation Test
  • Kinetics
  • Mutation
  • Phenylalanine-tRNA Ligase / genetics*
  • Phenylalanine-tRNA Ligase / metabolism
  • RNA, Transfer, Amino Acid-Specific / genetics*
  • RNA, Transfer, Phe / genetics*
  • RNA, Transfer, Phe / metabolism
  • Temperature

Substances

  • RNA, Transfer, Amino Acid-Specific
  • RNA, Transfer, Phe
  • Amino Acyl-tRNA Synthetases
  • Phenylalanine-tRNA Ligase