Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, Department of Microbiology, Nankai University, Tianjin 300071, China.
Biotechnol Lett. 2011 Sep;33(9):1823-30. doi: 10.1007/s10529-011-0626-4. Epub 2011 May 3.
A novel gene (IgASE2) encoding a C18-Δ9 polyunsaturated fatty acids specific (C18-Δ9-PUFAs-specific) elongase was isolated and characterized from DHA-rich microalga, Isochrysis galbana H29. The IgASE2 gene was 1,653 bp in length, contained a 786 bp ORF encoding a protein of 261 amino acids that shared 87% identity with Δ9 elongase, IgASE1, and possessed a 44 bp 5'-untranslated region (5'-UTR) and a 823 bp 3'-untranslated region (3'-UTR). IgASE2, by its heterologous expression in Saccharomyces cerevisiae, elongated linoleic acid (LA, 18:2n-6) and α-linolenic (ALA, 18:3n-3) to eicosadienoic acid (EDA, 20:2n-6) and eicosatrienoic acid (ETrA, 20:3n-3), respectively. The conversions of LA to EDA and ALA to ETrA were 57.6 and 56.1%, respectively. Co-expression of this elongase with Δ8 desaturase required for the synthesis of C20-polyunsaturated fatty acids resulted in the accumulation of dihomo-γ-linolenic acid (20:3n-6) from LA and eicosatetraenoic acid (20:4n-6) from ALA. These results demonstrated that IgASE2 exhibited C18-Δ9-PUFAs-specific elongase activity and the alternative Δ8 pathway was reconstituted.
从富含 DHA 的微藻球等鞭金藻中分离并鉴定了一个编码 C18-Δ9 多不饱和脂肪酸(C18-Δ9-PUFAs)特异性延伸酶的新基因(IgASE2)。IgASE2 基因长 1653bp,包含一个 786bp 的开放阅读框,编码一个 261 个氨基酸的蛋白质,与 Δ9 延伸酶、IgASE1 具有 87%的同源性,并具有 44bp 的 5′非翻译区(5′-UTR)和 823bp 的 3′非翻译区(3′-UTR)。IgASE2 在酿酒酵母中的异源表达将亚油酸(LA,18:2n-6)和α-亚麻酸(ALA,18:3n-3)分别延伸为二十碳二烯酸(EDA,20:2n-6)和二十碳三烯酸(ETrA,20:3n-3)。LA 转化为 EDA 和 ALA 转化为 ETrA 的转化率分别为 57.6%和 56.1%。该延伸酶与合成 C20 多不饱和脂肪酸所需的 Δ8 去饱和酶的共表达导致从 LA 积累二同型-γ-亚麻酸(20:3n-6)和从 ALA 积累二十碳四烯酸(20:4n-6)。这些结果表明 IgASE2 表现出 C18-Δ9-PUFAs 特异性延伸酶活性,并重建了替代的 Δ8 途径。