首页> 外文会议>International conference on applied biotechnology >Molecular Cloning, Characterization and Expression Analysis of a Gene Encoding Hydroxyphenylpyruvate Reductase Involved in Rosmarinic Acid Biosynthesis Pathway from Perilla frutescens
【24h】

Molecular Cloning, Characterization and Expression Analysis of a Gene Encoding Hydroxyphenylpyruvate Reductase Involved in Rosmarinic Acid Biosynthesis Pathway from Perilla frutescens

机译:紫苏迷迭香酸生物合成途径的羟苯丙酮酸还原酶编码基因的分子克隆,表征及表达分析

获取原文

摘要

In this study, a novel full-length cDNA of hydroxyphenylpyruvate reductase (HPPR) involved in rosmarinic acid (RA) biosynthesis pathway in Perilla frutescensis is cloned (designated as PfHPPR) for the first time by conserved fragment PCR and rapid amplification of cDNA ends (RACE). The cDNA of PfHPPR is 1723 bp long with an open reading frame (ORF) of 939 bp encoding a protein of 313 amino acid residues. Bioinformatics analysis revealed that the deduced amino acid sequence of PfHPPR has high homology to the other known HPPR proteins. Quantitative real-time PCR analysis of the transcription pattern indicates that the PfHPPR expresses constitutively in all examined tissues but most highly in leaf. Besides, the expression of PfHPPR can be induced by several factors such as abscisic acid (ABA), salicylic acid (SA), and ultraviolet-B radiation (UV-B).
机译:在这项研究中,通过保守片段PCR和cDNA末端的快速扩增,首次克隆了参与紫苏紫苏迷迭香酸(RA)生物合成途径的羟基苯基丙酮酸还原酶(HPPR)的全长全长cDNA。种族)。 PfHPPR的cDNA长1723 bp,开放阅读框(ORF)939 bp,编码313个氨基酸残基。生物信息学分析表明,推导的PfHPPR氨基酸序列与其他已知的HPPR蛋白具有高度同源性。转录模式的实时定量PCR分析表明,PfHPPR在所有检查的组织中组成性表达,但在叶中表达最高。此外,PfHPPR的表达可以由脱落酸(ABA),水杨酸(SA)和紫外线-B辐射(UV-B)等多种因素诱导。

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