青蒿
青蒿素
同位素
甲戊酸途径
生物合成
萜类
化学
立体化学
生物化学
生物
恶性疟原虫
有机化学
酶
分子
疟疾
免疫学
作者
Nicholas Schramek,Huahong Wang,Werner Römisch‐Margl,Birgit Keil,Tanja Radykewicz,Bernhard Winzenhörlein,Ludger Beerhues,Adelbert Bacher,Felix Rohdich,Jonathan Gershenzon,Benye Liu,Wolfgang Eisenreich
出处
期刊:Phytochemistry
[Elsevier BV]
日期:2009-11-24
卷期号:71 (2-3): 179-187
被引量:154
标识
DOI:10.1016/j.phytochem.2009.10.015
摘要
Artemisinin from Artemisia annua has become one of the most important drugs for malaria therapy. Its biosynthesis proceeds via amorpha-4,11-diene, but it is still unknown whether the isoprenoid precursors units are obtained by the mevalonate pathway or the more recently discovered non-mevalonate pathway. In order to address that question, a plant of A. annua was grown in an atmosphere containing 700 ppm of 13CO2 for 100 min. Following a chase period of 10 days, artemisinin was isolated and analyzed by 13C NMR spectroscopy. The isotopologue pattern shows that artemisinin was predominantly biosynthesized from (E,E)-farnesyl diphosphate (FPP) whose central isoprenoid unit had been obtained via the non-mevalonate pathway. The isotopologue data confirm the previously proposed mechanisms for the cyclization of (E,E)-FPP to amorphadiene and its oxidative conversion to artemisinin. They also support deprotonation of a terminal allyl cation intermediate as the final step in the enzymatic conversion of FPP to amorphadiene and show that either of the two methyl groups can undergo deprotonation.
科研通智能强力驱动
Strongly Powered by AbleSci AI