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从头合成苯甲基葡萄糖硫苷在大肠杆菌中的应用。

De novo production of benzyl glucosinolate in Escherichia coli.

机构信息

DynaMo Center, Copenhagen Plant Science Centre, Department of Plant and Environmental Sciences, Faculty of Science, University of Copenhagen, Thorvaldsensvej 40, 1871 Frederiksberg C, Denmark.

DynaMo Center, Copenhagen Plant Science Centre, Department of Plant and Environmental Sciences, Faculty of Science, University of Copenhagen, Thorvaldsensvej 40, 1871 Frederiksberg C, Denmark.

出版信息

Metab Eng. 2019 Jul;54:24-34. doi: 10.1016/j.ymben.2019.02.004. Epub 2019 Mar 1.

Abstract

Microbial production of plant specialised metabolites is challenging as the biosynthetic pathways are often complex and can contain enzymes, which function is not supported in traditional production hosts. Glucosinolates are specialised metabolites of strong commercial interest due to their health-promoting effects. In this work, we engineered the production of benzyl glucosinolate in Escherichia coli. We systematically optimised the production levels by first screening different expression strains and by modification of growth conditions and media compositions. This resulted in production from undetectable to approximately 4.1 μM benzyl glucosinolate, but also approximately 3.7 μM of desulfo-benzyl glucosinolate, the final intermediate of this pathway. Additional optimisation of pathway flux through entry point cytochrome P450 enzymes and PAPS-dependent sulfotransferase increased the production additionally 5-fold to 20.3 μM (equivalent to 8.3 mg/L) benzyl glucosinolate.

摘要

微生物生产植物特有的代谢物具有挑战性,因为生物合成途径通常很复杂,并且可能包含在传统生产宿主中功能不支持的酶。由于其具有促进健康的作用,硫代葡萄糖苷是具有强烈商业兴趣的特有的代谢物。在这项工作中,我们通过工程化方法在大肠杆菌中生产苄基硫代葡萄糖苷。我们通过首先筛选不同的表达菌株并通过修改生长条件和培养基组成来系统地优化生产水平。这导致苄基硫代葡萄糖苷的产量从无法检测到约 4.1µM,但也导致大约 3.7µM 的去磺基苄基硫代葡萄糖苷,这是该途径的最终中间体。通过入口处细胞色素 P450 酶和 PAPS 依赖性磺基转移酶进一步优化途径通量,将产量额外增加 5 倍,达到 20.3µM(相当于 8.3mg/L)苄基硫代葡萄糖苷。

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