Structural and Mechanistic Basis for Nitrile Synthetase by an Argininosuccinate Synthetase-Like Enzyme

The enzymatic origins of nitrile groups in fungal natural products have recently been linked to argininosuccinate synthetase (ASS)-like enzymes, but the structural basis for their unique catalytic function remained unknown. Here, we provide the structural and mechanistic elucidation of this enzyme class by characterizing ArtA, the nitrile synthetase from the auranthine biosynthetic pathway. High-resolution crystal structures of ArtA, combined with mutagenesis and molecular dynamics simulations, reveal how the canonical ASS active site is remodeled to selectively bind l-glutamine and catalyze nitrile formation through an elegant ATP-dependent elimination reaction. Furthermore, phylogenetic analysis and functional validation of homologues from another fungus (Fusarium) and a bacterium (Streptomyces) demonstrate that ArtA belongs to a widespread family of nitrile synthetases, likely acquired by fungi via horizontal gene transfer. Our work provides the molecular blueprint for this new enzyme family and opens avenues for genome mining and biocatalyst engineering.

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Publication Details

Journal
ACS Catalysis
Published
2025-09-05
DOI
https://doi.org/10.1021/acscatal.5c04243
Citations
1
Primary Topic
Amino Acid Enzymes and Metabolism
Type
article
Field-Weighted Citation Impact
1.11

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article

Structural and Mechanistic Basis for Nitrile Synthetase by an Argininosuccinate Synthetase-Like Enzyme

Tiantian Lu, Xinjian Yin, Honglei Ma, Xuefeng Lü et al.
1 citations
ACS Catalysis
Amino Acid Enzymes and Metabolism
1.11
article

Structural and Mechanistic Basis for Nitrile Synthetase by an Argininosuccinate Synthetase-Like Enzyme

Tiantian Lu, Xinjian Yin, Honglei Ma, Xuefeng Lü, Qiang Wang, Lan Liu, Zhizeng Gao, Jing Li, Keke Zhang, Longwei Xiong, Yujing Zeng, Heng Guo
article en
1 citations

Abstract

The enzymatic origins of nitrile groups in fungal natural products have recently been linked to argininosuccinate synthetase (ASS)-like enzymes, but the structural basis for their unique catalytic function remained unknown. Here, we provide the structural and mechanistic elucidation of this enzyme class by characterizing ArtA, the nitrile synthetase from the auranthine biosynthetic pathway. High-resolution crystal structures of ArtA, combined with mutagenesis and molecular dynamics simulations, reveal how the canonical ASS active site is remodeled to selectively bind l-glutamine and catalyze nitrile formation through an elegant ATP-dependent elimination reaction. Furthermore, phylogenetic analysis and functional validation of homologues from another fungus (Fusarium) and a bacterium (Streptomyces) demonstrate that ArtA belongs to a widespread family of nitrile synthetases, likely acquired by fungi via horizontal gene transfer. Our work provides the molecular blueprint for this new enzyme family and opens avenues for genome mining and biocatalyst engineering.

ACS CatalysisVol. 15(18)
Sun Yat-sen University (CN), JW Medical Systems (China) (CN), Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) (CN), Marine Research Centre (MV), Qingdao Institute of Bioenergy and Bioprocess Technology (CN)
Special Project for Marine Economy Development of Guangdong Province, National Natural Science Foundation of China, Natural Science Foundation of Shandong Province, Taishan Scholar Project of Shandong Province, National Key Research and Development Program of China
Openalex Percentile: Top 19%
Amino Acid Enzymes and Metabolism
1.11
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