Studies on in vitro DNA synthesis. Purification of the dna G gene product from Escherichia coli

Proc Natl Acad Sci U S A. 1973 May;70(5):1613-8. doi: 10.1073/pnas.70.5.1613.

Abstract

varphiX174 DNA-dependent dNMP incorporation is temperature-sensitive (ts) in extracts of uninfected E. coli dna A, B, C, D, E, and G ts strains. DNA synthesis can be restored in heat-inactivated extracts of various dna ts mutants by addition of extracts of wild-type or other dna ts mutants. A protein that restores activity to heat-inactivated extracts of dna G ts cells has been extensively purified. This protein has also been purified from dna G ts cells and is thermolabile when compared to the wild-type protein. The purified dna G protein has a molecular weight of about 60,000, is insensitive to N-ethylmaleimide, and binds poorly to DNA. It does not stimulate heat-inactivated crude extracts of dna B, C, D, or E ts cells and lacks detectable RNA and DNA polymerase activities.

MeSH terms

  • Ammonium Sulfate
  • Bacterial Proteins / isolation & purification*
  • Binding Sites
  • Centrifugation, Density Gradient
  • Chromatography, DEAE-Cellulose
  • Chromatography, Gel
  • DNA Replication
  • DNA, Bacterial / biosynthesis*
  • Dithiothreitol
  • Edetic Acid
  • Escherichia coli / growth & development
  • Escherichia coli / metabolism*
  • Freezing
  • Genes*
  • Genetic Complementation Test
  • Glycerol
  • Methods
  • Mutation
  • Streptomycin
  • Sulfates
  • Temperature

Substances

  • Bacterial Proteins
  • DNA, Bacterial
  • Sulfates
  • Edetic Acid
  • Glycerol
  • Ammonium Sulfate
  • Dithiothreitol
  • Streptomycin