High-level expression of a sika deer (Cervus nippon) Cu/Zn superoxide dismutase in Pichia pastoris and its characterization

Environ Toxicol Pharmacol. 2013 Mar;35(2):185-92. doi: 10.1016/j.etap.2012.11.013. Epub 2012 Dec 3.

Abstract

Production of a sika deer Cu/Zn-SOD was achieved in Pichia pastoris after the reconstituted expression vector pPIC9K was transformed into the strain GS115. By employing Saccharomyces cerevisiae secretion signal peptide (α-factor) under the regulation of the methanol-inducible promoter of the gene of alcohol oxidase 1 (AOX1), sika deer Cu/Zn-SOD with a molecular mass of 16kDa was expressed while recombinant sika deer Cu/Zn-SOD with an activity of 3500U/mL was obtained from a 5L bioreactor. After two successive steps of chromatography on DEAE-650C and Superdex75, recombinant sika deer Cu/Zn-SOD was obtained with 13.8% yield, 14.5-fold purification, and a specific activity of 3447U/mg. Its optimum temperature and optimum pH were 40°C and 7.0, respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Bioreactors
  • Cloning, Molecular
  • Deer / genetics*
  • Hydrogen-Ion Concentration
  • Molecular Sequence Data
  • Pichia / genetics*
  • Pichia / metabolism
  • Promoter Regions, Genetic
  • Recombinant Proteins / genetics*
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism
  • Saccharomyces cerevisiae / genetics
  • Superoxide Dismutase / genetics*
  • Superoxide Dismutase / metabolism*
  • Temperature

Substances

  • Recombinant Proteins
  • Superoxide Dismutase