Biosynthesis and engineering of isoprenoid small molecules |
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Authors: | Sydnor T. Withers Jay D. Keasling |
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Affiliation: | (1) Department of Chemical Engineering, University of California, Berkeley, CA, USA;(2) Department of Bioengineering, University of California, Berkeley, CA, USA;(3) Berkeley Center for Synthetic Biology, Physical Bioscience Division, Lawrence Berkeley National Laboratory, 717 Potter Street, Building 977, Mail code 3224, Berkeley, CA 94720-3224, USA;(4) California Institute for Quantitative Biomedical Research (QB3), University of California, Berkeley, CA, USA |
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Abstract: | Isoprenoid secondary metabolites are a rich source of commercial products that have not been fully explored. At present, there are isoprenoid products used in cancer therapy, the treatment of infectious diseases, and crop protection. All isoprenoids share universal prenyl diphosphate precursors synthesized via two distinct pathways. From these universal precursors, the biosynthetic pathways to specific isoprenoids diverge resulting in a staggering array of products. Taking advantage of this diversity has been the focus of much effort in metabolic engineering heterologous hosts. In addition, the engineering of the mevalonate pathway has increased levels of the universal precursors available for heterologous production. Finally, we will describe the efforts to produce to commercial terpenoids, paclitaxel and artemisinin. |
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Keywords: | Isoprenoids Terpenes Synthetic biology Metabolic engineering Artemisinin |
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