首页> 外文会议>3rd China-Japan-Korea Workshop on Sweetpotato(第三届中日韩甘薯学术研讨会)论文集 >Cloning of dihydroflavonol 4-reductase gene from sweetpotato Ipomoea batatas(L.)Lam.)and its expression in E.coli
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Cloning of dihydroflavonol 4-reductase gene from sweetpotato Ipomoea batatas(L.)Lam.)and its expression in E.coli

机译:甘薯番薯叶二氢黄酮醇4-还原酶基因的克隆及其在大肠杆菌中的表达

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Based on the conserved sequences of genes encoding djhydroflavonol 4-reductase(DFR)from other plants,primers were designed to amplify DFR gene from sweetpotato,the gene was designate Elesignated ibDFR in this paper.The gene has 1232 bp nucleotide and encoded 398aa.Sequence comparison revealed that ibDFR sequence shared homologies of 85%,67% and 75% with those of Ipomoea purpurea,tobacco and potato.The opening read fragment of ibDFR was inserted with pET 30 a(+)using lingase to detect the expression of ibDFR in E.coli strain BL 21(DE 3).The result showed that the molecular weight of ibDFR was consistent with the calculated ones.
机译:根据其他植物中编码djhydroflavonol 4-reasease(DFR)的基因保守序列,设计引物扩增甘薯中的DFR基因,该基因命名为Elesignated ibDFR,该基因全长1232 bp,编码398aa。比较表明,ibDFR序列与番薯,烟草和马铃薯具有相同的同源性,分别为85%,67%和75%。ibDFR的开放阅读片段插入有pET 30 a(+),并用连接酶检测了ibDFR在大肠杆菌中的表达。大肠杆菌BL 21(DE 3)菌株。结果表明,ibDFR的分子量与计算值一致。

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