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通过温度诱导系统和代谢工程合成酪醇和羟基酪醇。

Synthesis of Tyrosol and Hydroxytyrosol through Temperature-Inducible Systems and Metabolic Engineering.

作者信息

Chen Xiaochuan, Qian Tao, Wei Wenping, Zhu Yihui, Cai Gaopan, Li Mengfan, Chu Xiaohe, Ye Bang-Ce

机构信息

Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology, Zhejiang, Hangzhou 310014, China.

Laboratory of Biosystems and Microanalysis, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, China.

出版信息

ACS Synth Biol. 2025 Jun 20;14(6):2294-2304. doi: 10.1021/acssynbio.5c00172. Epub 2025 May 23.

Abstract

Hydroxytyrosol (HT) has various biological and pharmacological activities, including potent antioxidant activity. The efficient synthesis of HT and tyrosol has been achieved by microbial synthesis. However, more strategies are needed to enhance its yield and meet the demands of industrialization. In this study, and were used for the synthesis of tyrosol in using a temperature-inducible system. Different sources of phenolic acid decarboxylase and alcohol reductase were investigated, with and from showing the best catalytic performance, yielding 4.05 g/L of tyrosol at 60 h in shake flasks, the highest yield reported. Next, from BL21 (DE3) was introduced for HT biosynthesis, and the HT-related degradation gene was functionally characterized in . Subsequently, by enhancing precursor supply, eliminating competing metabolic pathways, and knocking out , the HT yield reached 1.28 g/L after 60 h. Finally, in a 5 L bioreactor, titers of 6.18 and 4.97 g/L of tyrosol and HT were achieved for the first time using a temperature-induced strategy. This study presents a method for the modification of microbial chassis for the efficient synthesis of tyrosol and HT.

摘要

羟基酪醇(HT)具有多种生物和药理活性,包括强大的抗氧化活性。通过微生物合成已实现了HT和酪醇的高效合成。然而,需要更多策略来提高其产量并满足工业化需求。在本研究中,利用温度诱导系统,使用[具体物质1]和[具体物质2]在[具体微生物]中合成酪醇。研究了不同来源的酚酸脱羧酶和醇还原酶,来自[具体微生物]的[具体酶1]和[具体酶2]表现出最佳催化性能,在摇瓶中60小时时酪醇产量达到4.05 g/L,这是报道的最高产量。接下来,将来自[具体微生物] BL21(DE3)的[具体酶3]引入用于HT生物合成,并在[具体微生物]中对与HT相关的降解基因[具体基因]进行了功能表征。随后,通过增强前体供应、消除竞争代谢途径和敲除[具体基因],60小时后HT产量达到1.28 g/L。最后,在5 L生物反应器中,首次使用温度诱导策略实现了酪醇和HT的滴度分别为6.18和4.97 g/L。本研究提出了一种用于修饰微生物底盘以高效合成酪醇和HT的方法。

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