A synthetic pathway for the production of 2-hydroxyisovaleric acid in Escherichia coli
| Autor: | Ramon Gonzalez, James M. Clomburg, Seokjung Cheong |
|---|---|
| Rok vydání: | 2017 |
| Předmět: |
0301 basic medicine
Glycerol 030106 microbiology Bioengineering Context (language use) medicine.disease_cause Applied Microbiology and Biotechnology Biological pathway Metabolic engineering 03 medical and health sciences chemistry.chemical_compound Synthetic biology Pyruvic Acid medicine Escherichia coli Valerates chemistry.chemical_classification Escherichia coli Proteins Amino acid Kinetics 030104 developmental biology Biochemistry chemistry Metabolic Engineering Synthetic Biology Flux (metabolism) Biotechnology |
| Zdroj: | Journal of industrial microbiologybiotechnology. 45(7) |
| ISSN: | 1476-5535 |
| Popis: | Synthetic biology, encompassing the design and construction of novel artificial biological pathways and organisms and the redesign of existing natural biological systems, is rapidly expanding the number of applications for which biological systems can play an integral role. In the context of chemical production, the combination of synthetic biology and metabolic engineering approaches continues to unlock the ability to biologically produce novel and complex molecules from a variety of feedstocks. Here, we utilize a synthetic approach to design and build a pathway to produce 2-hydroxyisovaleric acid in Escherichia coli and demonstrate how pathway design can be supplemented with metabolic engineering approaches to improve pathway performance from various carbon sources. Drawing inspiration from the native pathway for the synthesis of the 5-carbon amino acid l-valine, we exploit the decarboxylative condensation of two molecules of pyruvate, with subsequent reduction and dehydration reactions enabling the synthesis of 2-hydroxyisovaleric acid. Key to our approach was the utilization of an acetolactate synthase which minimized kinetic and regulatory constraints to ensure sufficient flux entering the pathway. Critical host modifications enabling maximum product synthesis from either glycerol or glucose were then examined, with the varying degree of reduction of these carbons sources playing a major role in the required host background. Through these engineering efforts, the designed pathway produced 6.2 g/L 2-hydroxyisovaleric acid from glycerol at 58% of maximum theoretical yield and 7.8 g/L 2-hydroxyisovaleric acid from glucose at 73% of maximum theoretical yield. These results demonstrate how the combination of synthetic biology and metabolic engineering approaches can facilitate bio-based chemical production. |
| Databáze: | OpenAIRE |
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