Functional expression of an omega-3 fatty acid desaturase gene from Glycine max in Saccharomyces cerevisiae.
- Author:
Hong-Tao ZHANG
1
;
Jia-Sen YANG
;
Lei SHAN
;
Yu-Ping BI
Author Information
1. High-Tech Research Center, Shandong Academy of Agricultural Sciences, Key Laboratory for Genetic Improvement of Crop Animal and Poultry of Shandong Province, Ji'nan 250100, China.
- Publication Type:Journal Article
- MeSH:
Chromatography, Gas;
Cloning, Molecular;
Fatty Acid Desaturases;
biosynthesis;
genetics;
Saccharomyces cerevisiae;
genetics;
metabolism;
Soybeans;
enzymology;
genetics;
alpha-Linolenic Acid;
analysis;
biosynthesis;
genetics
- From:
Chinese Journal of Biotechnology
2006;22(1):33-38
- CountryChina
- Language:Chinese
-
Abstract:
Alpha-linolenic acid(ALA, C18:3delta9,12,15 ) is an essential fatty acid which has many sanitary functions to human. However, its contents in diets are often not enough. In plants, omega-3 fatty acid desaturases(FAD) catalyze linoleic acid(LA, C18:2delta9,12) into ALA. The seed oil of Glycine max contains high level of ALA. To investigate the functions of Glycine max omega-3FAD, the cDNA of GmFAD3 C was amplified by RT-PCR from immature seeds, then cloned into the shuttle expression vector p416 to generate the recombinant vector p4GFAD3C. The resulting vector was transformed into Saccharomyces cerevisiae K601 throuth LiAc method. The positive clones were screened on the CM(Ura-) medium and identified by PCR, and then cultured in CM (Ura-) liquid medium with exogenous LA in 20 degrees C for three days. The intracellular fatty acid composition of the engineering strain Kp416 and Kp4GFAD3C was analyzed by gas chromatography (GC). A novel peak in strain Kp4GFAD3C was detected,which was not detectable in control, Comparison of the retention times of the newly yielded peak with that of authentic standard indicated that the fatty acid is ALA. The content of ALA reached to 3.1% of the total fatty acid in recombinant strain, the content of LA correspondingly decreased from 22% to 16.2% by contrast. It was suggested that the protein encoded by GmFAD3 C can specifically catalyze 18 carbon PUFA substrate of LA into ALA by taking off hydrogen atoms at delta15 location. In this study, we expressed a Glycine max omega-3 fatty acid desaturase gene in S. cerevisiae; An efficient and economical yeast expressing system(K601-p416 system) which is suitable for the expression of FAD was built.
