A novel D-amino acid oxidase from a contaminated agricultural soil metagenome and its characterization

Antonie Van Leeuwenhoek. 2015 Jun;107(6):1615-23. doi: 10.1007/s10482-015-0457-8. Epub 2015 Apr 22.

Abstract

A novel D-amino acid oxidase (DAAO) gene designated as daoE was cloned by the sequence-based screening of a plasmid metagenomic library of uncultured microorganisms from contaminated agricultural soil. The deduced amino acid sequence comparison and phylogenetic analysis indicated that daoE and other putative DAAOs are closely related. The putative DAAO gene was subcloned into a pETBlue-2 vector and overexpressed in Escherichia coli Tunner(DE3)pLacI. The recombinant protein was purified to homogeneity. The maximum activity of DaoE protein occurred at pH 8.0 and 37 °C. DaoE recombinant protein had an apparent K m of 2.96 mM, V max of 0.018 mM/min, k cat of 10.9/min, and k cat/K m of 1.16 × 10(4)/mol/min. The identification of this novel DAAO gene demonstrated the importance of metagenomic libraries in exploring new D-amino acid oxidases from environmental microorganisms to optimize their applications.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Cloning, Molecular
  • D-Amino-Acid Oxidase / genetics
  • D-Amino-Acid Oxidase / isolation & purification*
  • D-Amino-Acid Oxidase / metabolism*
  • Enzyme Stability
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Gene Library
  • Hydrogen-Ion Concentration
  • Kinetics
  • Metagenome*
  • Molecular Sequence Data
  • Phylogeny
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism
  • Sequence Homology, Amino Acid
  • Soil Microbiology*
  • Temperature

Substances

  • Recombinant Proteins
  • D-Amino-Acid Oxidase

Associated data

  • GENBANK/KP202181