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

被引:81
作者
Wagner, Martin [1 ]
Hoppe, Katharina [1 ]
Czabany, Tibor [2 ]
Heilmann, Mareike [1 ]
Daum, Guenther [2 ]
Feussner, Ivo [1 ]
Fulda, Martin [1 ]
机构
[1] Univ Gottingen, Dept Plant Biochem, Albrecht von Haller Inst Plant Sci, Gottingen, Germany
[2] Graz Univ Technol, Inst Biochem, A-8010 Graz, Austria
关键词
DGAT2; Fatty acids; Microalgae; Neutral lipid metabolism; Ostreococcus tauri; Triacylglycerol; ENCODING DIACYLGLYCEROL ACYLTRANSFERASE; PARIETOCHLORIS-INCISA TREBUXIOPHYCEAE; COA-MONOACYLGLYCEROL ACYLTRANSFERASE; YEAST SACCHAROMYCES-CEREVISIAE; TRIACYLGLYCEROL BIOSYNTHESIS; CHOLESTEROL ACYLTRANSFERASE; DOCOSAHEXAENOIC ACID; ARABIDOPSIS-THALIANA; ARACHIDONIC-ACID; LIPID PARTICLES;
D O I
10.1016/j.plaphy.2010.03.008
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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.
引用
收藏
页码:407 / 416
页数:10
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