Identification of a fatty acid ∆6-desaturase gene from the eicosapentaenoic acid-producing fungus Pythium splendens RBB-5

2012 ◽  
Vol 35 (3) ◽  
pp. 431-438 ◽  
Author(s):  
Ruijiao Zhang ◽  
Yuanmin Zhu ◽  
Liang Ren ◽  
Pengpeng Zhou ◽  
Jingrong Hu ◽  
...  
2011 ◽  
Vol 77 (11) ◽  
pp. 3870-3876 ◽  
Author(s):  
Takumi Kobayashi ◽  
Keishi Sakaguchi ◽  
Takanori Matsuda ◽  
Eriko Abe ◽  
Yoichiro Hama ◽  
...  

ABSTRACTThraustochytrids, marine protists known to accumulate polyunsaturated fatty acids (PUFAs) in lipid droplets, are considered an alternative to fish oils as a source of PUFAs. The major fatty acids produced in thraustochytrids are palmitic acid (C16:0),n− 6 docosapentaenoic acid (DPA) (C22:5n− 6), and docosahexaenoic acid (DHA) (C22:6n− 3), with eicosapentaenoic acid (EPA) (C20:5n− 3) and arachidonic acid (AA) (C20:4n− 6) as minor constituents. We attempted here to alter the fatty acid composition of thraustochytrids through the expression of a fatty acid Δ5 desaturase gene driven by the thraustochytrid ubiquitin promoter. The gene was functionally expressed inAurantiochytrium limacinummh0186, increasing the amount of EPA converted from eicosatetraenoic acid (ETA) (C20:4n− 3) by the Δ5 desaturase. The levels of EPA and AA were also increased by 4.6- and 13.2-fold in the transgenic thraustochytrids compared to levels in the mock transfectants when ETA and dihomo-γ-linolenic acid (DGLA) (C20:3n− 6) were added to the culture at 0.1 mM. Interestingly, the amount of EPA in the transgenic thraustochytrids increased in proportion to the amount of ETA added to the culture up to 0.4 mM. The rates of conversion and accumulation of EPA were much higher in the thraustochytrids than in baker's yeasts when the desaturase gene was expressed with the respective promoters. This report describes for the first time the finding that an increase of EPA could be accomplished by introducing the Δ5 desaturase gene into thraustochytrids and indicates that molecular breeding of thraustochytrids is a promising strategy for generating beneficial PUFAs.


2013 ◽  
Vol 144 (5) ◽  
pp. S-596
Author(s):  
Giulia Piazzi ◽  
Giuseppe D'Argenio ◽  
Vincenzo Lembo ◽  
Giovanna Mazzone ◽  
Anna Prossomariti ◽  
...  

2008 ◽  
Vol 17 (4) ◽  
pp. 717-725 ◽  
Author(s):  
Guiming Zhu ◽  
Hongxing Chen ◽  
Xiaojie Wu ◽  
Yanrong Zhou ◽  
Jianshen Lu ◽  
...  

Microbiology ◽  
2004 ◽  
Vol 150 (6) ◽  
pp. 1983-1990 ◽  
Author(s):  
Takahiro Oura ◽  
Susumu Kajiwara

Fungi, like plants, are capable of producing the 18-carbon polyunsaturated fatty acids linoleic acid and α-linolenic acid. These fatty acids are synthesized by catalytic reactions of Δ12 and ω3 fatty acid desaturases. This paper describes the first cloning and functional characterization of a yeast ω3 fatty acid desaturase gene. The deduced protein encoded by the Saccharomyces kluyveri FAD3 gene (Sk-FAD3) consists of 419 amino acids, and shows 30–60 % identity with Δ12 fatty acid desaturases of several eukaryotic organisms and 29–31 % identity with ω3 fatty acid desaturases of animals and plants. During Sk-FAD3 expression in Saccharomyces cerevisiae, α-linolenic acid accumulated only when linoleic acid was added to the culture medium. The disruption of Sk-FAD3 led to the disappearance of α-linolenic acid in S. kluyveri. These findings suggest that Sk-FAD3 is the only ω3 fatty acid desaturase gene in this yeast. Furthermore, transcriptional expression of Sk-FAD3 appears to be regulated by low-temperature stress in a manner different from the other fatty acid desaturase genes in S. kluyveri.


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