The isolation and characterization of the major glutathione S-transferase from the squid Loligo vulgaris

Comp Biochem Physiol B. 1991;98(4):511-5. doi: 10.1016/0305-0491(91)90245-9.

Abstract

1. The major glutathione S-transferase (GST) from the common squid Loligo vulgaris has been purified and shown to be a homodimer of subunit molecular mass 24,000 and pI 6.8. 2. It has high activity towards 1-chloro-2,4-dinitrobenzene, p-nitrobenzyl chloride, 4-hydroxynon-2-enal and linoleic acid hydroperoxide, low activity with 1,2-dichloro-4-nitrobenzene and no activity with ethacrynic acid, trans-4-phenyl-3-buten-2-one and 1,2-epoxy-3-(p-nitrophenoxy)propane. 3. The L. vulgaris GST did not cross-react with any of the available polyclonal antibodies raised against mammalian GSTs. 4. Forty amino acids of its N-terminal sequence have been determined. 5. Its activities and primary structure are compared with related proteins from other species.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Chromatography, High Pressure Liquid
  • Decapodiformes / enzymology*
  • Electrophoresis, Polyacrylamide Gel
  • Glutathione Transferase / chemistry
  • Glutathione Transferase / isolation & purification*
  • Glutathione Transferase / metabolism
  • Immunoblotting
  • Isoelectric Point
  • Isoenzymes / chemistry
  • Isoenzymes / isolation & purification*
  • Macromolecular Substances
  • Molecular Sequence Data
  • Molecular Weight
  • Substrate Specificity

Substances

  • Isoenzymes
  • Macromolecular Substances
  • Glutathione Transferase