Expression of Yb1 glutathione S-transferase using a baculovirus expression system

Biochem Biophys Res Commun. 1989 Aug 15;162(3):1147-54. doi: 10.1016/0006-291x(89)90793-6.

Abstract

A full-length cDNA clone was isolated for rat liver Yb1 glutathione S-transferase (EC 2.5.1.18). The coding sequence of Yb1 cDNA was inserted into a baculovirus vector for infection of Spodoptera frugiperda (SF9) cells. The enzymatically active recombinant Yb1 glutathione S-transferase protein has a native molecular weight of 42,000 daltons (by molecular sieve chromatography), a subunit molecular weight of 26,500 daltons (by SDS-polyacrylamide gel electrophoresis), a pI of 8.4 and an extinction coefficient E1%280 of 5.6 +/- 0.4.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA / genetics
  • Gene Expression Regulation
  • Genetic Vectors*
  • Glutathione Transferase / genetics*
  • Glutathione Transferase / metabolism
  • Insect Viruses / genetics*
  • Plasmids
  • Rats
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism
  • Substrate Specificity

Substances

  • Recombinant Proteins
  • DNA
  • Glutathione Transferase