Designing an oxidase toolbox for site-directed oxidation of taxanes

Paclitaxel is one of the most prominent drugs for cancer therapy, and its synthesis has long been pursued by scientific community. Although the biosynthetic pathway has been gradually unraveled, its synthetic efficiency remains severely constrained by the low activity and low product selectivity of the hydrolases involved. In this study, an artificial toolbox of oxidases derived from mutants of TteUPO (unspecific peroxygenase from Thielavia terrestris) is developed for site-directed oxidation of taxanes at the C-4, C-6, C-10, C-11, C-12, and C-13 positions. Furthermore, de novo biosynthesis of oxidized taxadiene products is achieved in an engineered E. coli chassis. These findings offer an unconventional strategy for developing an efficient route toward paclitaxel and constructing paclitaxel analogs with different structures for medicinal evaluation.

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Publication Details

Journal
Nature Communications
Published
2025-12-17
DOI
https://doi.org/10.1038/s41467-025-67544-4
Primary Topic
Cancer Treatment and Pharmacology
Type
article
Field-Weighted Citation Impact
0.00

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article

Designing an oxidase toolbox for site-directed oxidation of taxanes

Zhi‐Jun Zhang, Yu Wei Weng, Ran Hong, Hangcheng Li et al.
Nature Communications
Cancer Treatment and Pharmacology
article

Designing an oxidase toolbox for site-directed oxidation of taxanes

Zhi‐Jun Zhang, Yu Wei Weng, Ran Hong, Hangcheng Li, Jian Wei, Jian‐He Xu, Xinyi Lu, Hui‐Lei Yu, Zhengyu Huang, Lili Zhu, Longhao Huang, Mingyuan Lai
article en

Abstract

Paclitaxel is one of the most prominent drugs for cancer therapy, and its synthesis has long been pursued by scientific community. Although the biosynthetic pathway has been gradually unraveled, its synthetic efficiency remains severely constrained by the low activity and low product selectivity of the hydrolases involved. In this study, an artificial toolbox of oxidases derived from mutants of TteUPO (unspecific peroxygenase from Thielavia terrestris) is developed for site-directed oxidation of taxanes at the C-4, C-6, C-10, C-11, C-12, and C-13 positions. Furthermore, de novo biosynthesis of oxidized taxadiene products is achieved in an engineered E. coli chassis. These findings offer an unconventional strategy for developing an efficient route toward paclitaxel and constructing paclitaxel analogs with different structures for medicinal evaluation.

Nature CommunicationsVol. 17(1)
East China University of Science and Technology (CN), Shanghai Institute of Organic Chemistry (CN)
National Natural Science Foundation of China, Shanghai Jiao Tong University, National Key Research and Development Program of China
Openalex Percentile: Top 44%
Cancer Treatment and Pharmacology
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