Expression of soluble recombinant lipoxygenase from Pleurotus sapidus in Pichia pastoris

Protein Expr Purif. 2014 Mar:95:233-9. doi: 10.1016/j.pep.2014.01.004. Epub 2014 Jan 15.

Abstract

The first heterologous expression of an iron-containing lipoxygenase from a basidiomycete in Pichia pastoris is reported. Five different expression constructs of the lipoxygenase gene LOX1 from Pleurotus sapidus were cloned and successfully transferred into P. pastoris SMD1168, but only one pPIC9K vector construct was functionally expressed. In this construct the vector-provided α-factor signal sequence was replaced by insertion of a second Kozak sequence between the signal sequence and the LOX1 gene. His(+) transformants were screened for their level of resistance to geneticin (G418). Lox1 was expressed under different culture conditions and purified using the N-terminal His-tag. Relative enzyme activity increased significantly 48h after methanol induction and was highest with 2mll(-1) inducer. The recombinant enzyme showed an optimal lipoxygenase activity at pH 7 and 30-35°C and a vmax like the wild-type enzyme.

Keywords: Functional expression; Kozak sequence; Lipoxygenase; Pichia pastoris; Pleurotus sapidus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Fungal Proteins / chemistry
  • Fungal Proteins / genetics
  • Fungal Proteins / isolation & purification
  • Fungal Proteins / metabolism*
  • Hydrogen-Ion Concentration
  • Lipoxygenase / chemistry
  • Lipoxygenase / genetics
  • Lipoxygenase / isolation & purification
  • Lipoxygenase / metabolism*
  • Mass Spectrometry
  • Pichia / genetics
  • Pichia / metabolism*
  • Pleurotus / enzymology
  • Pleurotus / genetics*
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism*
  • Solubility
  • Temperature

Substances

  • Fungal Proteins
  • Recombinant Proteins
  • Lipoxygenase