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从 DHA 生产的小球藻 H29 中分离出一种新型的 C18-Δ9 多不饱和脂肪酸特异性延伸酶基因,并将其用于在酿酒酵母中重建替代的 Δ8 途径。

Isolation of a novel C18-Δ9 polyunsaturated fatty acid specific elongase gene from DHA-producing Isochrysis galbana H29 and its use for the reconstitution of the alternative Δ8 pathway in Saccharomyces cerevisiae.

机构信息

Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, Department of Microbiology, Nankai University, Tianjin 300071, China.

出版信息

Biotechnol Lett. 2011 Sep;33(9):1823-30. doi: 10.1007/s10529-011-0626-4. Epub 2011 May 3.

Abstract

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.

摘要

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。

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