Cloning and Functional Identification of Delta5 Fatty Acid Desaturase Gene and Its 5′-Upstream Region from Marine Fungus Thraustochytrium sp. FJN-10

被引:13
|
作者
Huang, Jian-Zhong [1 ,2 ,3 ]
Jiang, Xian-Zhang [1 ,2 ,3 ]
Xia, Xiao-Feng [1 ,2 ,3 ]
Yu, Ai-Qun [1 ,2 ,3 ]
Mao, Ruo-Yu [1 ,2 ,3 ]
Chen, Xiao-Feng [1 ,2 ,3 ]
Tian, Bao-Yu [1 ,2 ,3 ]
机构
[1] Fujian Normal Univ, Engn Res Ctr Ind Microbiol, Minist Educ, Fuzhou 350108, Fujian, Peoples R China
[2] Fujian Normal Univ, Engn Res Ctr Fujian Modern Fermentat Technol, Fuzhou 350108, Fujian, Peoples R China
[3] Fujian Normal Univ New Campus, Coll Life Sci, Fuzhou 350108, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Desaturase; Promoter; Thraustochytrium; Polyunsaturated fatty acid; Docosahexaenoic acid; TRANSCRIPTIONAL REGULATION; HETEROLOGOUS EXPRESSION; DOCOSAHEXAENOIC ACID; PROMOTER; BIOSYNTHESIS; MICROALGA; ELONGASE; YEAST; ADR1;
D O I
10.1007/s10126-010-9262-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A gene encoding delta5 fatty acid desaturase (fad5) was cloned from marine fungus Thraustochytrium sp. FJN-10, a species capable of producing docosahexaenoic acid. The open reading frame of fad5 was 1,320 bp and encoded a protein comprising 439 amino acids. Expression of the fad5 in Saccharomyces cerevisiae INVSC1 revealed that FAD5 is able to introduce a double bond at position 5 of the dihomo-gamma-linolenic acid (20:3 Delta(8,11,14)), resulting in arachidonic acid (20:4 Delta(5,8,11,14)) with a conversion rate of 56.40% which is the highest among engineering yeasts reported so far. The 5'-upstream region of fad5 was cloned by LA-PCR and analyzed. Phylogenetic analysis of this sequence with the 5'-upstream region of other delta5 desaturases showed that the 5'-upstream region of fad5 from Thraustochytrium share the smallest evolution distance with human and rhesus. Computational analysis of the nucleotide sequence of the 5'-upstream region of fad5 has revealed several basic transcriptional elements including five TATA boxes, three CCAAT boxes, 12 GC boxes, and several putative target-binding sites for transcription factors such as HSF, CAP, and ADR1. Preliminary functional analysis of this promoter in S. cerevisiae shows that the 5'-upstream region of fad5 could drive the expression of green fluorescent protein.
引用
收藏
页码:12 / 21
页数:10
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