| Literature DB >> 24623472 |
Tyler P Korman1, Bobby Sahachartsiri, Dan Li, Jeffrey M Vinokur, David Eisenberg, James U Bowie.
Abstract
The high yields required for the economical production of chemicals and fuels using microbes can be difficult to achieve due to the complexities of cellular metabolism. An alternative to performing biochemical transformations in microbes is to build biochemical pathways in vitro, an approach we call synthetic biochemistry. Here we test whether the full mevalonate pathway can be reconstituted in vitro and used to produce the commodity chemical isoprene. We construct an in vitro synthetic biochemical pathway that uses the carbon and ATP produced from the glycolysis intermediate phosphoenolpyruvate to run the mevalonate pathway. The system involves 12 enzymes to perform the complex transformation, while providing and balancing the ATP, NADPH, and acetyl-CoA cofactors. The optimized system produces isoprene from phosphoenolpyruvate in ∼100% molar yield. Thus, by inserting the isoprene pathway into previously developed glycolysis modules it may be possible to produce isoprene and other acetyl-CoA derived isoprenoids from glucose in vitro.Entities:
Keywords: biofuel; commodity chemicals; green chemistry; in vitro synthesis; isoprenoids; metabolic engineering
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Year: 2014 PMID: 24623472 PMCID: PMC4005709 DOI: 10.1002/pro.2436
Source DB: PubMed Journal: Protein Sci ISSN: 0961-8368 Impact factor: 6.725