Modular multi-enzyme cascades enable green and sustainable synthesis of non-canonical amino acids from glycerol

Non-canonical amino acids (ncAAs) bearing diverse functional groups hold transformative potential in drug discovery, protein engineering, and biomaterial science. However, their industrial-scale production remains constrained by the inefficiency, high cost, and environmental burden of conventional chemical and enzymatic methods. Here, we present a modular multi-enzyme cascade platform that leverages glycerol-an abundant and sustainable byproduct of biodiesel production-as a low-cost substrate for ncAAs synthesis. Directed evolution of O-phospho-L-serine sulfhydrylase (OPSS) enhances the catalytic efficiency of C-N bond formation by 5.6-fold, enabling the efficient synthesis of triazole-functionalized ncAAs. By integrating a plug-and-play enzymatic strategy, our system enables gram- to decagram-scale production of 22 ncAAs with C-S, C-Se, and C-N side chains and can be readily scaled up to a 2 liter reaction system. Notably, water is the sole byproduct, and all products exhibit an atomic economy of >75%, highlighting the environmental compatibility of this platform. This work establishes a green, cost-effective, and industrially viable approach to expanding amino acid diversity, providing a versatile toolkit for applications in pharmaceuticals, synthetic biology, and next-generation biomaterials.

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Publication Details

Journal
Nature Communications
Published
2025-08-29
DOI
https://doi.org/10.1038/s41467-025-63341-1
Citations
4
Primary Topic
Biochemical and Molecular Research
Type
article
Field-Weighted Citation Impact
3.22

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article

Modular multi-enzyme cascades enable green and sustainable synthesis of non-canonical amino acids from glycerol

Longwei Lou, Ulrich Schwaneberg, Feng Cheng, Zhimin Li et al.
4 citations
Nature Communications
Biochemical and Molecular Research
3.22
article

Modular multi-enzyme cascades enable green and sustainable synthesis of non-canonical amino acids from glycerol

Longwei Lou, Ulrich Schwaneberg, Feng Cheng, Zhimin Li, Shuhong Wang, Zonglin Li, Shuai Xu, Yu Ji
article en
4 citations

Abstract

Non-canonical amino acids (ncAAs) bearing diverse functional groups hold transformative potential in drug discovery, protein engineering, and biomaterial science. However, their industrial-scale production remains constrained by the inefficiency, high cost, and environmental burden of conventional chemical and enzymatic methods. Here, we present a modular multi-enzyme cascade platform that leverages glycerol-an abundant and sustainable byproduct of biodiesel production-as a low-cost substrate for ncAAs synthesis. Directed evolution of O-phospho-L-serine sulfhydrylase (OPSS) enhances the catalytic efficiency of C-N bond formation by 5.6-fold, enabling the efficient synthesis of triazole-functionalized ncAAs. By integrating a plug-and-play enzymatic strategy, our system enables gram- to decagram-scale production of 22 ncAAs with C-S, C-Se, and C-N side chains and can be readily scaled up to a 2 liter reaction system. Notably, water is the sole byproduct, and all products exhibit an atomic economy of >75%, highlighting the environmental compatibility of this platform. This work establishes a green, cost-effective, and industrially viable approach to expanding amino acid diversity, providing a versatile toolkit for applications in pharmaceuticals, synthetic biology, and next-generation biomaterials.

Nature CommunicationsVol. 16(1)
East China University of Science and Technology (CN), State Key Laboratory of Chemical Engineering (CN), Chemical Synthesis Lab (SG), Zhejiang University of Technology (CN), Beijing University of Chemical Technology (CN), RWTH Aachen University (DE)
National Natural Science Foundation of China, National Key Research and Development Program of China
Responsible consumption and production
Openalex Percentile: Top 8%
Biochemical and Molecular Research
3.22
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