首页> 外文期刊>Journal of Agricultural and Food Chemistry >Molecular Cloning and Characterization of Hydroperoxide Lyase Gene in the Leaves of Tea Plant (Camellia sinensis)
【24h】

Molecular Cloning and Characterization of Hydroperoxide Lyase Gene in the Leaves of Tea Plant (Camellia sinensis)

机译:茶树叶片中过氧化氢裂解酶基因的分子克隆与鉴定

获取原文
获取原文并翻译 | 示例
       

摘要

Hydroperoxide lyase (HPL, E.C. 4.1.2.) is the major enzyme in the biosynthesis of natural volatile aldehydes and alcohols in plants, however, little was known about HPL in tea plants (Camellia sinensis). A unique cDNA fragment was isolated by suppressive subtractive hybridization (SSH) from a tea plant subjected to herbivory by tea geometrid Ectropis obliqua. This full length cDNA acquired by RACE was 1476 bp and encoded 491 amino acids. DNA and protein BLAST searches showed high homology to HPL sequences from other plants. The His-tag expression vector pET-32a(+)/CsHPL was constructed and transferred into Escherichia coli Rosetta (DE3). The expression product of recombinant CsHPL in E. coli was about 60 kDa. The enzyme activity of CsHPL was 0.20 mu mol.min(-1).mg(-1). Quantitative RT-PCR analysis indicated CsHPL was strongly up-regulated in tea plants after Ectropis obliqua attack, suggesting that it may be an important candidate for defense against insects in tea plants.
机译:氢过氧化物裂解酶(HPL,E.C. 4.1.2)是植物中天然挥发性醛和醇类生物合成中的主要酶,然而,关于茶树(Camellia sinensis)中的HPL知之甚少。通过抑制性消减杂交(SSH)从茶树几何学上的食斜E(Ectropis obliqua)吃草的茶树中分离出独特的cDNA片段。通过RACE获得的全长cDNA为1476 bp,编码491个氨基酸。 DNA和蛋白质BLAST搜索显示与其他植物的HPL序列高度同源。构建了His-tag表达载体pET-32a(+)/ CsHPL,并将其转移到大肠杆菌Rosetta(DE3)中。重组CsHPL在大肠杆菌中的表达产物约为60kDa。 CsHPL的酶活性为0.20μmol.min(-1).mg(-1)。定量RT-PCR分析表明,茶树Ectropis obliqua攻击后,CsHPL在茶树中强烈上调,这表明它可能是防御茶树中昆虫的重要候选物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号