The 110 kDa glutathione transferase of Yarrowia lipolytica is encoded by a homologue of the TEF3 gene from Saccharomyces cerevisiae: Cloning, expression, and homology modeling of the recombinant protein

Shane McGoldrick, Tommie V. McCarthy, David Sheehan

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

The TEF4 gene of the non-saccharomyces yeast Yarrowia lipolytica encodes an EF1Bγ protein with structural similarity to the glutathione transferases (GSTs). This 1203 bp gene was cloned, over-expressed in Escherichia coli, and the recombinant protein characterized. DNA sequencing of the cloned gene agreed with the recently completed Y. lipolytica genome and showed 100% identity to a previously reported 30-residue N-terminal sequence for a 110 kDa Y. lipolytica GST, except that it encoded two additional N-terminal residues (N-Met-Ser-). The recombinant protein (subunit Mr 52 kDa) was found not to possess GST activity with 1-chloro-2,4-dinitrobenzene. Partial tryptic digestion released two fragments of Mr 22 and 18 kDa, which we interpret as N- and C-terminal domains. Homology modeling confirmed that the N-terminal domain of Y. lipolytica TEF4 encodes a GST-like protein.

Original languageBritish English
Pages (from-to)1125-1132
Number of pages8
JournalBiochemical and Biophysical Research Communications
Volume337
Issue number4
DOIs
StatePublished - 2 Dec 2005

Keywords

  • Cloning
  • EF1Bγ
  • Elongation factor
  • Expression
  • Glutathione transferase
  • Recombinant
  • Sequence
  • TEF4
  • Yarrowia lipolytica
  • Yeast

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