从甲醇合成 α-法呢烯的光驱动体外酶促生物系统。

Q2 Agricultural and Biological Sciences 生物设计研究(英文) Pub Date : 2024-07-30 eCollection Date: 2024-01-01 DOI:10.34133/bdr.0039
Xinyue Gui, Fei Li, Xinyu Cui, Ranran Wu, Dingyu Liu, Chunling Ma, Lijuan Ma, Huifeng Jiang, Chun You, Zhiguang Zhu
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引用次数: 0

摘要

具有重大工业价值的萜类化合物主要通过直接从植物中提取获得。最近,微生物细胞工厂或体外酶生物系统已成为生产萜类化合物的有前途的替代方法。在此,我们报告了一条基于体外酶级联反应的 α-法呢烯合成路线,该反应使用甲醇作为廉价且可再生的 C1 底物。我们对分为 2 个模块的 13 个生物催化反应进行了优化和耦合,通过与天然类囊体膜的整合实现了甲醇-α-法呢烯的转化,成为一种绿色能源引擎。这种由光驱动的体外酶生物系统能以甲醇和中间体乙醛为底物,分别生产出 1.43 和 2.40 毫克升-1 α-法呢烯。这项工作为开发光动力体外生物合成平台提供了一种前景广阔的策略,从而生产出更多由 C1 底物合成的天然化合物。
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A Light-Driven In Vitro Enzymatic Biosystem for the Synthesis of α-Farnesene from Methanol.

Terpenoids of substantial industrial interest are mainly obtained through direct extraction from plant sources. Recently, microbial cell factories or in vitro enzymatic biosystems have emerged as promising alternatives for terpenoid production. Here, we report a route for the synthesis of α-farnesene based on an in vitro enzyme cascade reaction using methanol as an inexpensive and renewable C1 substrate. Thirteen biocatalytic reactions divided into 2 modules were optimized and coupled to achieve methanol-to-α-farnesene conversion via integration with natural thylakoid membranes as a green energy engine. This in vitro enzymatic biosystem driven by light enabled the production of 1.43 and 2.40 mg liter-1 α-farnesene using methanol and the intermediate glycolaldehyde as substrates, respectively. This work could provide a promising strategy for developing light-powered in vitro biosynthetic platforms to produce more natural compounds synthesized from C1 substrates.

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来源期刊
CiteScore
3.90
自引率
0.00%
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审稿时长
12 weeks
期刊最新文献
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