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大肠杆菌中抗抑郁药裸盖菇素的从头生物合成。

De Novo Biosynthesis of Antidepressant Psilocybin in Escherichia coli.

作者信息

Huang Zhangrao, Yao Yongpeng, Di Rouyu, Zhang JianChao, Pan Yuanyuan, Liu Gang

机构信息

State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, People's Republic of China.

University of Chinese Academy of Sciences, Beijing, People's Republic of China.

出版信息

Microb Biotechnol. 2025 Apr;18(4):e70135. doi: 10.1111/1751-7915.70135.

Abstract

Psilocybin, a tryptamine-derived alkaloid, has been granted Breakthrough Therapy designation by the U.S. FDA for treatment-resistant depression, underscoring its clinical importance. Therefore, sustainable and economic production is urgently needed. Manufacturing of psilocybin in Escherichia coli has drawn great attention. However, due to the low expression and activity of the eukaryotic cytochrome P450 enzyme PsiH in the psilocybin biosynthetic pathway, de novo synthesis of psilocybin in prokaryotic cells has been hampered. To overcome this dilemma, we herein demonstrated de novo synthesis of psilocybin in E. coli by constructing PsiH variants with N-terminal domain modifications and expressing the entire biosynthetic pathway at a concordantly low temperature. Improving the supply of precursor and engineering the P450 electron transfer chain resulted in a 33-fold increase in the titre of norbaeocystin (105.3 mg/L), a key intermediate of psilocybin biosynthesis, and a 17-fold increase in the titre of psilocybin (14 mg/L). Further enhancement of psilocybin production was achieved by converting norbaeocystin to psilocybin by overexpressing an extra copy of the methyltransferase gene psiM. Finally, 79.4 mg/L of psilocybin was produced by optimising flask fermentation conditions, a 100-fold improvement over the starting strain. Our work demonstrates the successful fungal P450 engineering to improve the catalytic activity in E. coli and will advance the sustainable production of the important antidepressant psilocybin in prokaryotic microbial cells.

摘要

裸盖菇素是一种源自色胺的生物碱,已被美国食品药品监督管理局授予治疗抵抗性抑郁症的突破性疗法认定,凸显了其临床重要性。因此,迫切需要可持续且经济的生产方式。在大肠杆菌中生产裸盖菇素已引起了广泛关注。然而,由于裸盖菇素生物合成途径中真核细胞色素P450酶PsiH的低表达和低活性,原核细胞中裸盖菇素的从头合成受到了阻碍。为克服这一困境,我们在此展示了通过构建具有N端结构域修饰的PsiH变体并在一致的低温下表达整个生物合成途径,在大肠杆菌中实现裸盖菇素的从头合成。改善前体供应并对P450电子传递链进行工程改造,使裸盖菇素生物合成的关键中间体降斑鸠菊酸的产量提高了33倍(105.3毫克/升),裸盖菇素的产量提高了17倍(14毫克/升)。通过过表达甲基转移酶基因psiM的额外拷贝将降斑鸠菊酸转化为裸盖菇素,进一步提高了裸盖菇素的产量。最后,通过优化摇瓶发酵条件,生产出了79.4毫克/升的裸盖菇素,比起始菌株提高了100倍。我们的工作展示了成功的真菌P450工程改造以提高大肠杆菌中的催化活性,并将推动在原核微生物细胞中可持续生产重要的抗抑郁药裸盖菇素。

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