4.7 Article

Identification and characterization of an acyl-CoA:diacylglycerol acyltransferase 2 (DGAT2) gene from the microalga O. tauri

Journal

PLANT PHYSIOLOGY AND BIOCHEMISTRY
Volume 48, Issue 6, Pages 407-416

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.plaphy.2010.03.008

Keywords

DGAT2; Fatty acids; Microalgae; Neutral lipid metabolism; Ostreococcus tauri; Triacylglycerol

Categories

Funding

  1. Fonds der Chemischen Industrie
  2. Union zur Forderung von Oelund Proteinpflanzen e. V.
  3. Bundesministerium fur Bildung und Forschung [0313637c]
  4. Graduate School for Neurosciences and Molecular Biosciences (GGNB) (DFG) [GSC 226/1]
  5. International Max Planck Research School at the Georg August University Gottingen
  6. Fonds zur Forderung der wissenschaftlichen Forschung in Osterreich [18857, W901-805]

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In order to identify novel genes encoding enzymes involved in the terminal step of triacylglycerol (TAG) formation, a database search was carried out in the genome of the unicellular photoautotrophic green alga Ostreococcus tauri. The search led to the identification of three putative type 2 acyl-CoA:diacylglycerol acyltransferase-like sequences (DGAT; EC 2.3.1.20), and revealed the absence of any homolog to type 1 or type 3 DGAT sequence in the genome of O. tauri. For two of the cDNA sequences (OtDGAT2A and B) enzyme activity was detected by heterologous expression in Saccharomyces cerevisiae mutant strains with impaired TAG metabolism. However, activity of OtDGAT2A was too low for further analysis. Analysis of their amino acid sequences showed that they share limited identity with other DGAT2 from different plant species, such as Ricinus communis and Vernicia fordii with similar to 25 to 30% identity. Lipid analysis of the mutant yeast cells revealed that OtDGAT2B showed broad substrate specificity accepting saturated as well as mono- and poly-unsaturated acyl-CoAs as substrates. (C) 2010 Elsevier Masson SAS. All rights reserved.

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