Department of Chemistry, University of California, Berkeley, Berkeley, CA, USA.
Department of Biological Sciences, University at Buffalo, State University of New York, Buffalo, NY, USA.
Nat Chem. 2021 Dec;13(12):1178-1185. doi: 10.1038/s41557-021-00820-0. Epub 2021 Nov 22.
Living systems provide a promising approach to chemical synthesis, having been optimized by evolution to convert renewable carbon sources, such as glucose, into an enormous range of small molecules. However, a large number of synthetic structures can still be difficult to obtain solely from cells, such as unsubstituted hydrocarbons. In this work, we demonstrate the use of a dual cellular-heterogeneous catalytic strategy to produce olefins from glucose using a selective hydrolase to generate an activated intermediate that is readily deoxygenated. Using a new family of iterative thiolase enzymes, we genetically engineered a microbial strain that produces 4.3 ± 0.4 g l of fatty acid from glucose with 86% captured as 3-hydroxyoctanoic and 3-hydroxydecanoic acids. This 3-hydroxy substituent serves as a leaving group that enables heterogeneous tandem decarboxylation-dehydration routes to olefinic products on Lewis acidic catalysts without the additional redox input required for enzymatic or chemical deoxygenation of simple fatty acids.
生物体系为化学合成提供了一种很有前景的方法,它们在进化过程中被优化,能够将可再生碳源(如葡萄糖)转化为大量的小分子。然而,仍然有大量的合成结构仅靠细胞难以获得,例如未取代的烃类。在这项工作中,我们展示了一种双重细胞-多相催化策略,利用选择性水解酶生成可轻易脱氧的活化中间产物,从而从葡萄糖中生产烯烃。我们利用一系列新的迭代硫酯酶酶,通过基因工程改造微生物菌株,使其从葡萄糖中生产 4.3 ± 0.4 g/L 的脂肪酸,其中 86%被捕获为 3-羟基辛酸和 3-羟基癸酸。这个 3-羟基取代基是一个离去基团,使得路易斯酸性催化剂上的多相串联脱羧-脱水反应路径能够生成烯烃产物,而无需酶促或化学脱除简单脂肪酸所需的额外氧化还原输入。