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首页> 外文期刊>Cell biochemistry and biophysics >Functional Characterization of Polyunsaturated Fatty Acid Delta 6-Desaturase and Elongase Genes from the Black Seabream (Acanthopagrus schlegelii)
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Functional Characterization of Polyunsaturated Fatty Acid Delta 6-Desaturase and Elongase Genes from the Black Seabream (Acanthopagrus schlegelii)

机译:黑鲷(Acanthopagrus schlegelii)多不饱和脂肪酸Delta 6-去饱和酶和延伸酶基因的功能表征

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Fatty acid delta 6-desaturase (D6DES) and elongases are key enzymes in the synthesis of polyunsaturated fatty acids (PUFAs) including arachidonic acid (ARA) and eicosapentaenoic acid (EPA) from microorganisms to higher animals. To identify the genes encoding D6DES and elongases for PUFAs, we isolated each cDNA with a high similarity to the D6DES and ELOVL5-like elongases of mammals and fishes via degenerate PCR and RACE-PCR from Acanthopagrus schlegelii. A recombinant vector expressing AsD6DES was subsequently constructed and transformed into Saccharomyces cerevisiae to test the enzymatic activity toward n-6 and n-3 fatty acids in the PUFA biosynthesis. The heterologously expressed AsD6DES produced γ-linolenic acid (GLA, C18:3 n-6) and stearidonic acid (STA, C18:4 n-3) at conversion rates of 26.3-35.6 % from exogenous linoleic acid (LA, C18:2 n-6) and α-linolenic acid (ALA, C18:3 n-3) substrates, respectively. When AsELOVL5 was expressed in yeast, it conferred an ability to elongate GLA to di-homo-γ-linolenic acid (DGLA, C20:3 n-6). In addition, AsELOVL5 showed an ability to convert ARA (C20:4 n-6) and EPA (C20:5 n-3) to dodecylthioacetic acid (DTA, C22:4 n-6) and docosapentaenoic acid (DPA, C22:5 n-3), respectively. In these results, the AsD6DES encodes a delta 6-fatty acid desaturase and the AsELOVL5 encoding a long-chain fatty acid elongase shows activity to enlongate C18Δ6/C20Δ5, but not C22.
机译:脂肪酸δ6-去饱和酶(D6DES)和延伸酶是从微生物到高等动物合成多不饱和脂肪酸(PUFA)的关键酶,包括花生四烯酸(ARA)和二十碳五烯酸(EPA)。为了鉴定编码PUFA的D6DES和延伸酶的基因,我们通过简并PCR和RACE-PCR从Acanthopagrus schlegelii中分离了与哺乳动物和鱼类的D6DES和ELOVL5样延伸酶高度相似的每个cDNA。随后构建表达AsD6DES的重组载体,并将其转化到啤酒酵母中以测试PUFA生物合成中对n-6和n-3脂肪酸的酶活性。异源表达的AsD6DES从外源亚油酸(LA,C18:2)转化率为26.3-35.6%,生成了γ-亚麻酸(GLA,C18:3 n-6)和硬脂酸(STA,C18:4 n-3)。 n-6)和α-亚麻酸(ALA,C18:3 n-3)底物。当AsELOVL5在酵母中表达时,它赋予了将GLA延长为二高纯γ-亚麻酸(DGLA,C20:3 n-6)的能力。此外,AsELOVL5具有将ARA(C20:4 n-6)和EPA(C20:5 n-3)转化为十二烷基硫代乙酸(DTA,C22:4 n-6)和二十二碳五烯酸(DPA,C22:5)的能力。 n-3)。在这些结果中,AsD6DES编码一个6-脂肪酸去饱和酶,而AsELOVL5编码一个长链脂肪酸延长酶则显示出延长C18Δ6/C20Δ5的活性,但没有延长C22的活性。

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