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Effect of Sugars on Artemisinin Production in Artemisia annua L.: Transcription and Metabolite Measurements

机译:糖对青蒿中青蒿素生产的影响:转录和代谢产物测定

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摘要

The biosynthesis of the valuable sesquiterpene anti-malarial, artemisinin, is known to respond to exogenous sugar concentrations. Here young Artemisia annua L. seedlings (strain YU) were used to measure the transcripts of six key genes in artemisinin biosynthesis in response to growth on sucrose, glucose, or fructose. The measured genes are: from the cytosolic arm of terpene biosynthesis, 3-hydroxy-3-methyl-glutaryl-CoA reductase (HMGR), farnesyl disphosphate (FPS); from the plastid arm of terpene biosynthesis, 1-deoxyxylulose-5-phosphate synthase (DXS), 1-deoxyxylulouse 5-phosphate reductoisomerase (DXR); from the dedicated artemisinin pathway amorpha-4,11-diene synthase (ADS), and the P450, CYP71AV1 (CYP). Changes in intracellular concentrations of artemisinin (AN) and its precursors, dihydroartemisinic acid (DHAA), artemisinic acid (AA), and arteannuin B (AB) were also measured in response to these three sugars. FPS, DXS, DXR, ADS and CYP transcript levels increased after growth in glucose, but not fructose. However, the kinetics of these transcripts over 14 days was very different. AN levels were significantly increased in glucose-fed seedlings, while levels in fructose-fed seedlings were inhibited; in both conditions this response was only observed for 2 days after which AN was undetectable until day 14. In contrast to AN, on day 1 AB levels doubled in seedlings grown in fructose compared to those grown in glucose. Results showed that transcript level was often negatively correlated with the observed metabolite concentrations. When seedlings were gown in increasing levels of AN, some evidence of a feedback mechanism emerged, but mainly in the inhibition of AA production. Together these results show the complex interplay of exogenous sugars on the biosynthesis of artemisinin in young A. annua seedlings.
机译:已知有价值的倍半萜抗疟疾青蒿素的生物合成对外源糖浓度有反应。在这里,青蒿幼苗(YU菌株)用于测量响应于蔗糖,葡萄糖或果糖生长的青蒿素生物合成中六个关键基因的转录本。测得的基因是:从萜烯生物合成的胞质臂,3-羟基-3-甲基-戊二酰-CoA还原酶(HMGR),法呢基二磷酸(FPS);来自萜烯生物合成的质体臂中的1-脱氧木酮糖5-磷酸合酶(DXS),1-脱氧木酮5-磷酸还原异构酶(DXR);来自青蒿素专用途径amorpha-4,11-diene合酶(ADS)和P450,CYP71AV1(CYP)。响应这三种糖,还测量了青蒿素(AN)及其前体二氢青蒿酸(DHAA),青蒿酸(AA)和青蒿素B(AB)的细胞内浓度变化。葡萄糖生长后FPS,DXS,DXR,ADS和CYP转录水平升高,但果糖未升高。但是,这些转录本在14天内的动力学差异很大。葡萄糖喂养的幼苗中AN水平显着升高,而果糖喂养的幼苗中AN水平受到抑制;在两种情况下,这种反应仅观察到2天,之后直到第14天才检测到AN。与AN相比,在第1天,果糖中生长的幼苗中的AB水平比葡萄糖中生长的AB翻了一倍。结果表明,转录水平通常与观察到的代谢物浓度呈负相关。当幼苗的AN含量增加时,出现了一些反馈机制的证据,但主要是抑制了AA的产生。这些结果共同表明,外源糖对青蒿幼苗中青蒿素生物合成的复杂相互作用。

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