Semi-synthetic artemisinin: a model for the use of synthetic biology in pharmaceutical development

被引:471
作者
Paddon, Chris J. [1 ]
Keasling, Jay D. [2 ,3 ,4 ,5 ]
机构
[1] Amyris Inc, Emeryville, CA 94608 USA
[2] Univ Calif Berkeley, Dept Chem & Biomol Engn, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Phys Biosci Div, Berkeley, CA 94720 USA
[5] Joint BioEnergy Inst, Emeryville, CA 94608 USA
关键词
ANTIMALARIAL-DRUG PRECURSOR; HIGH-LEVEL PRODUCTION; SACCHAROMYCES-CEREVISIAE; ISOPRENOID BIOSYNTHESIS; PLASMODIUM-FALCIPARUM; QINGHAOSU ARTEMISININ; PATHWAY OPTIMIZATION; PLANT SESQUITERPENES; PLASMID CONSTRUCTION; MICROBIAL-PRODUCTION;
D O I
10.1038/nrmicro3240
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Recent developments in synthetic biology, combined with continued progress in systems biology and metabolic engineering, have enabled the engineering of microorganisms to produce heterologous molecules in a manner that was previously unfeasible. The successful synthesis and recent entry of semi-synthetic artemisinin into commercial production is the first demonstration of the potential of synthetic biology for the development and production of pharmaceutical agents. In this Review, we describe the metabolic engineering and synthetic biology approaches that were used to develop this important antimalarial drug precursor. This not only demonstrates the incredible potential of the available technologies but also illuminates how lessons learned from this work could be applied to the production of other pharmaceutical agents.
引用
收藏
页码:355 / 367
页数:13
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