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用于生物合成咖啡酸衍生的苯乙酯和苯乙酰胺的酵母代谢工程

Yeast Metabolic Engineering for Biosynthesis of Caffeic Acid-Derived Phenethyl Ester and Phenethyl Amide.

作者信息

Jia Zi-Chen, Liu Duo, Ma Hai-Di, Cui Yu-Hui, Li Hui-Min, Li Xia, Yuan Ying-Jin

机构信息

Frontiers Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China.

Frontiers Research Institute for Synthetic Biology, Tianjin University, Tianjin 300072, China.

出版信息

ACS Synth Biol. 2023 Dec 15;12(12):3635-3645. doi: 10.1021/acssynbio.3c00413. Epub 2023 Nov 28.

Abstract

Caffeic acid (CA)-derived phenethyl ester (CAPE) and phenethyl amide (CAPA) are extensively investigated bioactive compounds with therapeutic applications such as antioxidant, anti-inflammatory, and anticarcinogenic properties. To construct microbial cell factories for production of CAPE or CAPA is a promising option given the limitation of natural sources for product extraction and the environmental toxicity of the agents used in chemical synthesis. We reported the successful biosynthesis of caffeic acid in yeast previously. Here in this work, we further constructed the downstream synthetic pathways in yeast for biosynthesis of CAPE and CAPA. After combinatorial engineering of yeast chassis based on the rational pathway engineering method and library-based SCRaMbLE method, we finally obtained the optimal strains that respectively produced 417 μg/L CAPE and 1081 μg/L CAPA. Two screened gene targets of ΔHAM1 and ΔYJL028W were discovered to help improve the product synthesis capacity. This is the first report of the synthesis of CAPA from glucose in an engineered yeast chassis. Future work on enzyme and chassis engineering will further support improving the microbial cell factories for the production of CA derivatives.

摘要

咖啡酸(CA)衍生的苯乙酯(CAPE)和苯乙酰胺(CAPA)是具有广泛研究的生物活性化合物,具有抗氧化、抗炎和抗癌等治疗应用特性。鉴于产品提取天然来源的局限性以及化学合成中所用试剂的环境毒性,构建用于生产CAPE或CAPA的微生物细胞工厂是一个有前景的选择。我们之前报道了在酵母中成功生物合成咖啡酸。在这项工作中,我们进一步在酵母中构建了用于CAPE和CAPA生物合成的下游合成途径。基于合理途径工程方法和基于文库的SCRaMbLE方法对酵母底盘进行组合工程后,我们最终获得了分别产生417μg/L CAPE和1081μg/L CAPA的最优菌株。发现两个筛选出的基因靶点ΔHAM1和ΔYJL028W有助于提高产品合成能力。这是在工程酵母底盘中从葡萄糖合成CAPA的首次报道。未来在酶和底盘工程方面的工作将进一步支持改进用于生产CA衍生物的微生物细胞工厂。

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