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利用可再生葡萄糖生产 2-苯乙醇的大肠杆菌代谢工程。

Metabolic engineering of Escherichia coli for production of 2-phenylethanol from renewable glucose.

机构信息

Synergetic Innovation Center of Food Safety and Nutrition, Wuxi, 214122, China,

出版信息

Appl Biochem Biotechnol. 2014 Feb;172(4):2012-21. doi: 10.1007/s12010-013-0659-3. Epub 2013 Dec 8.

Abstract

2-Phenylethanol (2-PE) is an important aromatic alcohol with a rose-like odor and has wide applications. The present work aims to construct a synthetic pathway for 2-PE synthesis from glucose in Escherichia coli. First, the genes adh1 (encoding alcohol dehydrogenase) and kdc (encoding phenylpyruvate decarboxylase) from Saccharomyces cerevisiae S288c and Pichia pastoris GS115 were investigated in E. coli, respectively, and single overexpression of adh1 or kdc significantly increased 2-PE accumulation. When co-overexpressing adh1 and kdc, 2-PE was increased up to 130 from 57 mg/L. Furthermore, by optimizing coordinated expression of the four committed genes aroF, pheA, adh1 and kdc, 2-PE was improved to 285 mg/L which was the highest production of 2-PE by the recombinant E. coli system. In addition, our results also demonstrated that the tyrB gene, which encodes aromatic-amino-acid transaminase, plays an important role on 2-PE synthesis.

摘要

2-苯乙醇(2-PE)是一种具有玫瑰香味的重要芳香醇,具有广泛的应用。本工作旨在构建大肠杆菌中从葡萄糖合成 2-PE 的合成途径。首先,研究了酿酒酵母 S288c 和巴斯德毕赤酵母 GS115 中的基因 adh1(编码醇脱氢酶)和 kdc(编码苯丙酮酸脱羧酶)在大肠杆菌中的表达情况,adh1 或 kdc 的单独过表达显著增加了 2-PE 的积累。当共表达 adh1 和 kdc 时,2-PE 从 57mg/L 增加到 130mg/L。此外,通过优化四个关键基因 aroF、pheA、adh1 和 kdc 的协调表达,将 2-PE 提高到 285mg/L,这是重组大肠杆菌系统中 2-PE 的最高产量。此外,我们的研究结果还表明,编码芳香族氨基酸转氨酶的 tyrB 基因在 2-PE 合成中起着重要作用。

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