Department of Bioengineering, University of California, Berkeley, Berkeley, California 94270, United States.
Department of Bioengineering, University of California, San Francisco, California 94143, United States.
ACS Synth Biol. 2020 Mar 20;9(3):468-474. doi: 10.1021/acssynbio.9b00402. Epub 2020 Mar 9.
Climate change necessitates the development of CO neutral or negative routes to chemicals currently produced from fossil carbon. In this paper we demonstrate a pathway from the renewable resource glucose to next generation biofuel isopentanol by pairing the isovaleryl-CoA biosynthesis pathway from and a butyryl-CoA reductase from . The best plasmid and strain combination makes 80.50 ± 8.08 (SD) mg/L of isopentanol after 36 h under microaerobic conditions with an oleyl alcohol overlay. In addition, the system also shows a strong preference for isopentanol production over prenol in microaerobic conditions. Finally, the pathway requires zero adenosine triphosphate and can be paired theoretically with nonoxidative glycolysis, the combination being redox balanced from glucose thus avoiding unnecessary carbon loss as CO. These pathway properties make the isovaleryl-CoA pathway an attractive isopentanol production route for further optimization.
气候变化需要开发 CO 中性或负性途径,以生产目前从化石碳中获得的化学品。在本文中,我们通过将来自 和来自 的丁酰 CoA 还原酶配对,展示了一条从可再生资源葡萄糖到下一代生物燃料异戊醇的途径。最佳质粒和 菌株组合在微氧条件下用油醇覆盖 36 小时后,可产生 80.50 ± 8.08(mg/L)的异戊醇,标准偏差为 8.08(mg/L)。此外,该系统在微氧条件下也表现出对异戊醇生产而不是prenol 的强烈偏好。最后,该途径不需要三磷酸腺苷,并可以理论上与非氧化糖酵解配对,该组合从葡萄糖开始就实现了氧化还原平衡,从而避免了作为 CO 的不必要的碳损失。这些途径特性使得异戊酰 CoA 途径成为进一步优化的有吸引力的异戊醇生产途径。