Identification and characterization of new Δ-17 fatty acid desaturases

Appl Microbiol Biotechnol. 2013 Mar;97(5):1973-85. doi: 10.1007/s00253-012-4068-2. Epub 2012 May 27.

Abstract

ω-3 fatty acid desaturase is a key enzyme for the biosynthesis of ω-3 polyunsaturated fatty acids via the oxidative desaturase/elongase pathways. Here we report the identification of three ω-3 desaturases from oomycetes, Pythium aphanidermatum, Phytophthora sojae, and Phytophthora ramorum. These new ω-3 desaturases share 55 % identity at the amino acid level with the known Δ-17 desaturase of Saprolegnia diclina, and about 31 % identity with the bifunctional Δ-12/Δ-15 desaturase of Fusarium monoliforme. The three enzymes were expressed in either wild-type or codon optimized form in an engineered arachidonic acid producing strain of Yarrowia lipolytica to study their activity and substrate specificity. All three were able to convert the ω-6 arachidonic acid to the ω-3 eicosapentanoic acid, with a substrate conversion efficiency of 54-65 %. These enzymes have a broad ω-6 fatty acid substrate spectrum, including both C18 and C20 ω-6 fatty acids although they prefer the C20 substrates, and have strong Δ-17 desaturase activity but weaker Δ-15 desaturase activity. Thus, they belong to the Δ-17 desaturase class. Unlike the previously identified bifunctional Δ-12/Δ-15 desaturase from F. monoliforme, they lack Δ-12 desaturase activity. The newly identified Δ-17 desaturases could use fatty acids in both acyl-CoA and phospholipid fraction as substrates. The identification of these Δ-17 desaturases provides a set of powerful new tools for genetic engineering of microbes and plants to produce ω-3 fatty acids, such as eicosapentanoic acid and docosahexanoic acid, at high levels.

MeSH terms

  • Amino Acid Sequence
  • Arachidonic Acid / metabolism
  • Biotransformation
  • Cloning, Molecular
  • Eicosapentaenoic Acid / metabolism
  • Fatty Acid Desaturases / genetics*
  • Fatty Acid Desaturases / metabolism*
  • Gene Expression
  • Models, Molecular
  • Molecular Sequence Data
  • Phytophthora / enzymology*
  • Phytophthora / genetics
  • Pythium / enzymology*
  • Pythium / genetics
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Saprolegnia / enzymology
  • Saprolegnia / genetics
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Substrate Specificity
  • Yarrowia / genetics

Substances

  • Recombinant Proteins
  • Arachidonic Acid
  • Eicosapentaenoic Acid
  • Fatty Acid Desaturases
  • omega-3 fatty acid desaturase