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首页> 外文期刊>Molecular Biology Reports >Molecular cloning, characterization and function analysis of the gene encoding HMG-CoA reductase from Euphorbia Pekinensis Rupr
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Molecular cloning, characterization and function analysis of the gene encoding HMG-CoA reductase from Euphorbia Pekinensis Rupr

机译:一品红HMG-CoA还原酶编码基因的分子克隆,鉴定及功能分析

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摘要

A new full-length cDNA encoding 3-hydroxy-3-methylglutoryl-Coenzyme A reductase (HMGR; EC1.1.1.34), which catalyzes the first committed step of isoprenoids biosynthesis in MVA pathway, was isolated from young leaves of Euphorbia Pekinensis Rupr. by rapid amplification of cDNA ends (RACE) for the first time. The full-length cDNA of HMGR (designated as EpHMGR, GenBank Accession NO. EF062569) was 2,200 bp containing a 1,752 bp ORF encoding 583 amino acids. Bioinformatic analyzes revealed that the deduced EpHMGR had extensive homology with other plant HMGRs and contained two transmembrane domains and a catalytic domain. The predicted 3-D model of EpHMGR had a typical spatial structure of HMGRs. Southern blot analysis indicated that at most two copies of EpHMGR gene existed in E. Pekinensis genome. Tissue expression analysis revealed that EpHMGR expressed strongly in roots, weakly in stems and leaves. The functional colour complementation assay indicated that EpHMGR could accelerate the biosynthesis of carotenoids in the Escherichia coli transformant, demonstrating that EpHMGR plays an influential role in isoprenoid biosynthesis. Keywords 3-Hydroxy-3-methylglutaryl-CoA reductase (HMGR) - RACE - Euphorbia pekinensis Rupr
机译:从大戟(Euphorbia Pekinensis Rupr)的幼叶中分离出编码3-羟基-3-甲基戊二酰辅酶A还原酶(HMGR; EC1.1.1.34)的新全长cDNA,该酶催化MVA途径中类异戊二烯生物合成的第一步。 。首次快速扩增cDNA末端(RACE)。 HMGR的全长cDNA(称为EpHMGR,GenBank登录号EF062569)为2,200bp,包含1,752bp的ORF,编码583个氨基酸。生物信息学分析表明,推导的EpHMGR与其他植物HMGR具有广泛的同源性,并包含两个跨膜结构域和一个催化结构域。 EpHMGR的预测3-D模型具有HMGR的典型空间结构。 Southern印迹分析表明,在北京大肠杆菌基因组中存在最多两个拷贝的EpHMGR基因。组织表达分析表明,EpHMGR在根中表达强,而在茎和叶中表达弱。功能性颜色互补分析表明,EpHMGR可以促进大肠杆菌转化体中类胡萝卜素的生物合成,表明EpHMGR在类异戊二烯的生物合成中具有重要作用。关键词3-羟基-3-甲基戊二酰辅酶A还原酶-RACE-大戟

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