Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA, USA.
Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA, USA.
Curr Opin Biotechnol. 2020 Dec;66:171-178. doi: 10.1016/j.copbio.2020.07.005. Epub 2020 Aug 24.
Isoprenoid biosynthesis has been a focus of metabolic engineering due to the broad spectrum of uses of isoprenoid products and the limited capacity to source them from plants or chemically synthesize them. Microbial synthesis offers the potential to cost-effectively produce isoprenoids in a stable and scalable manner. One bottleneck in advancing microbial engineering for isoprenoid biosynthesis has been limited supply of precursor molecules to the isoprenoid pathway. This article reviews strategies that have been employed to overcome such limitations. These include methods for enhancing reactions in the native pathway and preventing substrate depletion by competing pathways, the use of heterologous enzymes and pathways, and methods that reduce the metabolic burden imposed by heterologous reactions. Additionally, this article discusses challenges for the synthesis of novel products and maps some new directions for future research.
异戊二烯生物合成一直是代谢工程的重点,因为异戊二烯产物用途广泛,而从植物中获取或通过化学合成的能力有限。微生物合成为以经济有效的方式稳定且规模化地生产异戊二烯提供了可能。在推进微生物工程用于异戊二烯生物合成方面的一个瓶颈是异戊烯途径中前体分子的有限供应。本文综述了克服这些限制的策略。这些策略包括增强天然途径中反应的方法和通过竞争途径防止底物耗竭的方法、使用异源酶和途径的方法以及降低异源反应带来的代谢负担的方法。此外,本文还讨论了合成新型产物所面临的挑战,并为未来的研究指明了一些新的方向。