首页> 美国卫生研究院文献>other >Overexpression and Suppression of Artemisia annua 4-Hydroxy-3-Methylbut-2-enyl Diphosphate Reductase 1 Gene (AaHDR1) Differentially Regulate Artemisinin and Terpenoid Biosynthesis
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Overexpression and Suppression of Artemisia annua 4-Hydroxy-3-Methylbut-2-enyl Diphosphate Reductase 1 Gene (AaHDR1) Differentially Regulate Artemisinin and Terpenoid Biosynthesis

机译:青蒿4-羟基-3-甲基丁-2-烯基二磷酸还原酶1基因(AaHDR1)的过表达和抑制差异调节青蒿素和类萜生物合成。

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摘要

4-Hydroxy-3-methylbut-2-enyl diphosphate reductase (HDR) catalyzes the last step of the 2-C-methyl-D-erythritol 4- phosphate (MEP) pathway to synthesize isopentenyl pyrophosphate (IPP) and dimethylallyl diphosphate (DMAPP). To date, little is known regarding effects of an increase or a decrease of a HDR expression on terpenoid and other metabolite profiles in plants. In our study, an Artemisia annua HDR cDNA (namely AaHDR1) was cloned from leaves. Expression profiling showed that it was highly expressed in leaves, roots, stems, and flowers with different levels. Green florescence protein fusion and confocal microscope analyses showed that AaHDR1 was localized in chloroplasts. The overexpression of AaHDR1 increased contents of artemisinin, arteannuin B and other sesquiterpenes, and multiple monoterpenes. By contrast, the suppression of AaHDR1 by anti-sense led to opposite results. In addition, an untargeted metabolic profiling showed that the overexpression and suppression altered non-polar metabolite profiles. In conclusion, the overexpression and suppression of AaHDR1 protein level in plastids differentially affect artemisinin and other terpenoid biosynthesis, and alter non-polar metabolite profiles of A. annua. Particularly, its overexpression leading to the increase of artemisinin production is informative to future metabolic engineering of this antimalarial medicine.
机译:4-羟基-3-甲基丁-2-烯基二磷酸还原酶(HDR)催化2-C-甲基-D-赤藓糖醇4-磷酸(MEP)路径的最后一步,以合成焦磷酸异戊烯基酯(IPP)和二磷酸二甲基烯丙基酯(DMAPP) )。迄今为止,关于HDR表达增加或减少对植物中萜类化合物和其他代谢物谱的影响知之甚少。在我们的研究中,从叶片中克隆了青蒿HDR cDNA(即AaHDR1)。表达谱表明其在不同水平的叶,根,茎和花中高表达。绿色荧光蛋白融合和共聚焦显微镜分析表明,AaHDR1位于叶绿体中。 AaHDR1的过表达增加了青蒿素,青蒿素B和其他倍半萜以及多个单萜的含量。相比之下,反义抑制AaHDR1导致相反的结果。此外,未靶向的代谢谱分析表明过表达和抑制作用会改变非极性代谢物谱。总之,质体中AaHDR1蛋白水平的过表达和抑制作用会不同程度地影响青蒿素和其他萜类生物合成,并改变青蒿的非极性代谢物谱。特别是,其过表达导致青蒿素产量增加,为该抗疟药的未来代谢工程提供了信息。

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