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一种从葡萄糖生产烯烃的双细胞-多相催化剂策略。

A dual cellular-heterogeneous catalyst strategy for the production of olefins from glucose.

机构信息

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.

出版信息

Nat Chem. 2021 Dec;13(12):1178-1185. doi: 10.1038/s41557-021-00820-0. Epub 2021 Nov 22.

Abstract

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.

摘要

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。

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