Molecular cloning and regulation of expression of the genes for initiation factor 3 and two aminoacyl-tRNA synthetases

J Bacteriol. 1982 Oct;152(1):357-62. doi: 10.1128/jb.152.1.357-362.1982.

Abstract

A 22-kilobase fragment of the Escherichia coli chromosome which contains the genes for translation initiation factor 3, phenylalanyl-tRNA synthetase, and threonyl-tRNA synthetase was cloned into plasmid pACYC184. The hybrid plasmid (designated pID1) complements a temperature-sensitive pheS lesion in E. coli NP37. pID1-transformed NP37 overproduce initiation factor 3 and phenylalanyl-tRNA synthetase. Gene expression from pID1 was studied in vitro in a coupled transcription-translation system and in minicells. The results suggest that the genes for initiation factor 3 and phenylalanyl- and threonyl-tRNA synthetase are regulated by different mechanisms.

Publication types

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

MeSH terms

  • Amino Acyl-tRNA Synthetases / genetics*
  • Cloning, Molecular*
  • Escherichia coli / genetics
  • Gene Expression Regulation*
  • Genes, Bacterial*
  • Peptide Initiation Factors / biosynthesis
  • Peptide Initiation Factors / genetics*
  • Phenylalanine-tRNA Ligase / biosynthesis
  • Phenylalanine-tRNA Ligase / genetics
  • Plasmids
  • Prokaryotic Initiation Factor-3
  • Threonine-tRNA Ligase / biosynthesis
  • Threonine-tRNA Ligase / genetics

Substances

  • Peptide Initiation Factors
  • Prokaryotic Initiation Factor-3
  • Amino Acyl-tRNA Synthetases
  • Phenylalanine-tRNA Ligase
  • Threonine-tRNA Ligase