首页> 外文期刊>Molecular biology reports >Molecular cloning and functional expression analysis of a new gene encoding geranylgeranyl diphosphate synthase from hazel (Corylus avellana L. Gasaway).
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Molecular cloning and functional expression analysis of a new gene encoding geranylgeranyl diphosphate synthase from hazel (Corylus avellana L. Gasaway).

机译:榛树编码香叶基香叶基二磷酸合酶的新基因的分子克隆和功能表达分析。

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摘要

Geranylgeranyl diphosphate synthase (GGPPS) [EC 2.5.1.29] catalyzes the biosynthesis of geranylgeranyl diphosphate (GGPP), which is a key precursor for diterpenes such as taxol. Herein, a full-length cDNA encoding GGPPS (designated as CgGGPPS) was cloned and characterized from hazel (Corylus avellana L. Gasaway), a taxol-producing angiosperms. The full-length cDNA of CgGGPPS was 1515 bp with a 1122 bp open reading frame (ORF) encoding a 373 amino acid polypeptide. The CgGGPPS genomic DNA sequence was also obtained, revealing CgGGPPS gene was not interrupted by an intron. Southern blot analysis indicated that CgGGPPS belonged to a small gene family. Tissue expression pattern analysis indicated that CgGGPPS expressed the highest in leaves. RT-PCR analysis indicated that CgGGPPS expression could be induced by exogenous methyl jasmonate acid. Furthermore, carotenoid accumulation was observed in Escherichia coli carrying pACCAR25 Delta crtE plasmid carrying CgGGPPS. The result revealed that cDNA encoded a functional GGPP synthase.
机译:Geranylgeranyl diphosphate合酶(EC 2.5.1.29)催化Geranylgeranyl diphosphate(GGPP)的生物合成,它是二萜类化合物如紫杉醇的关键前体。在此,从产生紫杉醇的被子植物榛子(Corylus avellana L.Gasaway)中克隆并鉴定了编码GGPPS的全长cDNA(称为CiGGPPS )。 CgGGPPS的全长cDNA为1515 bp,带有1122 bp的开放阅读框(ORF),编码373个氨基酸。还获得了CgGGPPS基因组DNA序列,表明 CgGGPPS 基因没有被内含子打断。 Southern印迹分析表明 CgGGPPS 属于一个小基因家族。组织表达模式分析表明,CgGGPPS在叶片中表达最高。 RT-PCR分析表明,外源茉莉酸甲酯可诱导CgGGPPS表达。此外,在携带pACCAR25ΔcrtE质粒的大肠杆菌中观察到了类胡萝卜素的积累,所述质粒携带有CgGGPPS。结果显示cDNA编码功能性GGPP合酶。

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