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Nicotiana benthamiana as a production platform for artemisinin precursors

机译:烟草:本氏烟草作为青蒿素前体的生产平台

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摘要

BACKGROUND: Production of pharmaceuticals in plants provides an alternative for chemical synthesis, fermentation or natural sources. Nicotiana benthamianais deployed at commercial scale for production of therapeutic proteins. Here the potential of this plant is explored for rapid production ofprecursors of artemisinin, a sesquiterpenoid compound that is used for malaria treatment. METHODOLOGY/PRINCIPAL FINDINGS: Biosynthetic genes leading to artemisinic acid, a precursor of artemisinin, were combined and expressed in N. benthamiana by agro-infiltration. The first committed precursor of artemisinin, amorpha-4,11-diene, was produced upon infiltration of a constructcontaining amorpha-4,11-diene synthase, accompanied by 3-hydroxy-3-methylglutaryl-CoA reductase and farnesyl diphosphate synthase. Amorpha-4,11-diene was detected both in extracts and in the headspace of the N. benthamiana leaves. When the amorphadiene oxidase CYP71AV1 was co-infiltrated with the amorphadiene-synthesizing construct, the amorpha-4,11-diene levels strongly decreased, suggesting it was oxidized. Surprisingly, no anticipated oxidation products, such as artemisinic acid, were detected upon GC-MS analysis. However, analysis of leaf extracts with a non-targeted metabolomics approach, using LC-QTOF-MS, revealed the presence ofanother compound, which was identified as artemisinic acid-12-beta-diglucoside. This compound accumulated to 39.5 mg x kg(-1) fwt. Apparently the product of the heterologous pathway that was introduced, artemisinic acid, is further metabolized efficiently by glycosyl transferases that are endogenous to N. benthamiana. CONCLUSION/SIGNIFICANCE: This work shows that agroinfiltration of N. bentamiana can be used as a model to study the production of sesquiterpenoid pharmaceutical compounds. The interaction between the ectopically introduced pathway and the endogenous metabolism of the plant is discussed.
机译:背景:在植物中生产药物为化学合成,发酵或天然来源提供了替代方法。本氏烟草以商业规模部署用于生产治疗性蛋白质。在这里,该植物的潜力被开发用于快速生产青蒿素的前体,青蒿素是一种用于治疗疟疾的倍半萜类化合物。方法学/主要发现:合成青蒿素(青蒿素的前体)的生物合成基因在农杆菌中通过农业浸润表达。青蒿素的第一个定型前体是amorpha-4,11-diene,是通过渗透含有amorpha-4,11-diene合酶以及3-羟基-3-甲基戊二酰-CoA还原酶和法呢基二磷酸合酶的构建物而产生的。在本氏烟草叶的提取物中和顶空都检测到了Amorpha-4,11-diene。当将吗啡二烯氧化酶CYP71AV1与合成吗啡二烯的构建体共同浸润时,吗啡4,11-二烯的含量大大降低,表明它已被氧化。令人惊讶地,在GC-MS分析中未检测到预期的氧化产物,例如青蒿酸。但是,使用LC-QTOF-MS采用非靶向代谢组学方法对叶提取物进行分析,结果表明存在另一种化合物,该化合物被鉴定为青蒿酸-12-β-二葡萄糖苷。该化合物累积至39.5 mg x kg(-1)fwt。显然,引入的异源途径的产物青蒿酸被本氏烟草内生的糖基转移酶进一步有效地代谢。结论/意义:这项工作表明,本氏烟草的农杆菌浸润可以用作研究倍半萜类药物化合物生产的模型。讨论了异位导入途径与植物内源代谢之间的相互作用。

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