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首页> 外文期刊>Comparative biochemistry and physiology, Part B. Biochemistry & molecular biology >Characterization and comparison of fatty acyl A6 desaturase cDNAs from freshwater and marine teleost fish species
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Characterization and comparison of fatty acyl A6 desaturase cDNAs from freshwater and marine teleost fish species

机译:淡水和硬骨鱼类鱼类脂肪酰基A6脱氢酶cDNA的表征和比较

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Fish are the most important dietary source of the n-3 highly unsaturated fatty acids(HUFA),eicosapentaenoic(EPA)and docosahexaenoic acid(DHA),that have particularly important roles in human nutrition reflecting their roles in critic"al physiological processes.The objective of the study described here was to clone,functionally characterize and compare expressed fatty acid desaturase genes involved in the production of EPA and DHA in freshwater and marine teleost fish species.Putative fatty acid desaturase cDNAs were isolated and cloned from common carp {Cyprinus carpio)and turbot(Psetta maximus).The enzymic activities of the products of these cDNAs,together with those of cDNAs previously cloned from rainbow trout(Oncorhynchus mykiss)and gilthead sea bream {Spams aurata),were determined by heterologous expression in the yeast Saccharomyces cerevisiae.The carp and turbot desaturase cDNAs included open reading frames(ORFs)of 1335 and 1338 base pairs,respectively,specifying proteins of 444 and 445 amino acids.The protein sequences possessed all the characteristic features of microsomal fatty acid desaturases,including three histidine boxes,two transmembrane regions,and N-terminal cytochrome b_ domains containing the haem-binding motif,HPGG.Functional expression showed all four fish cDNAs encode basically unifunctional A6 fatty acid desaturase enzymes responsible for the first and rate-limiting step in the biosynthesis of HUFA from 18:3n-3 and 18:2n-6.All the fish desaturases were more active towards the n-3 substrate with 59.5%,31.5%,23.1% and 7.0% of 18:3n-3 being converted to 18:4n-3 in the case of turbot,trout,sea bream and carp,respectively.The enzymes also showed very low,probably physiologically insignificant,levels of A5 desaturase activity,but none of the products showed A4 desaturase activity.The cloning and characterization of desaturases from these fish is an important advance,as they are species in which there is a relative wealth of data on the nutritional regulation of fatty acid desaturation and HUFA synthesis,and between which substantive differences occur.
机译:鱼类是n-3高不饱和脂肪酸(HUFA),二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)的最重要饮食来源,它们在人类营养中具有特别重要的作用,反映了它们在批评性生理过程中的作用。本文所述研究的目的是克隆,功能鉴定和比较表达淡水和海水硬骨鱼类中EPA和DHA产生的脂肪酸去饱和酶基因。从鲤鱼中分离并克隆了预期的脂肪酸去饱和酶cDNAs(Cyprinus carpio )和大菱t(Psetta maximus)。这些cDNA的产物以及先前从虹鳟鱼(Oncorhynchus mykiss)和金头鲷(Spams aurata)克隆的cDNA的酶活性由酵母酵母中的异源表达确定鲤鱼和大菱turbo去饱和酶cDNA包含1335个碱基对和1338个碱基对的开放阅读框(ORF),分别指定444个蛋白该蛋白质序列具有微粒体脂肪酸去饱和酶的所有特征,包括三个组氨酸盒,两个跨膜区和含有血红素结合基序HPGG的N端细胞色素b_结构域。 cDNA基本上编码单功能的A6脂肪酸去饱和酶,这是HUFA从18:3n-3和18:2n-6进行生物合成的第一步和限速步骤。所有鱼去饱和酶对n-3底物的活性更高,在turbo鱼,鳟鱼,鲷鱼和鲤鱼的情况下,分别将18:3n-3的59.5%,31.5%,23.1%和7.0%转换为18:4n-3。这些酶也显示非常低,可能在生理上是微不足道的A5去饱和酶的活性水平,但没有一种产品显示A4去饱和酶的活性。这些鱼的去饱和酶的克隆和鉴定是一个重要的进步,因为它们是其中营养成分相对丰富的数据。脂肪酸去饱和和HUFA合成的调节,两者之间存在实质性差异。

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