Lid loop-mediated proton transfer revealed in the Fe/αKG-dependent decarboxylase TraH

TraH, a fungal decarboxylase from Penicillium crustosum, belongs to the isopenicillin N synthase (IPNS) subfamily of non-heme iron/α-ketoglutarate (αKG)-dependent enzymes. IPNS enzymes are characterized by N- and C-terminal insertions that can reshape the active site. However, the functional and mechanistic roles of these elements, particularly in fungal decarboxylases, remain largely unexplored. Here, we report crystal structures of TraH in complex with various substrates, revealing a N-terminal loop, serving as lid and undergoes substrate-dependent dynamic conformational rearrangements. Upon binding of crustosic acid, this lid loop forms a hydrogen-bonding network to stabilize a water molecule, which mediates interaction between the conserved K191 residue in the DSBH (double-stranded β-helix) core and the substrate. Mutagenesis and QM/MM metadynamics simulations suggest that proton transfer from K191 is mediated by water molecules stabilized by the lid loop, supporting a decarboxylation mechanism distinct from the canonical strategy of direct carboxylate stabilization by DBSH core-located basic residues in other αKG-dependent decarboxylases. Interestingly, this loop is dispensable for the desaturation of crustosic acid methyl ester, thereby pinpointing its essential role to the precise positioning of the carboxylate substrate for proton transfer during decarboxylation. Evolutionary and structural analyses reveal significant variation in lid loop composition across IPNS enzymes, indicating its contribution to substrate recognition and functional diversification. Overall, our findings uncover a regulatory element in iron/αKG-dependent enzymes and offer insights into how non-core structural elements contribute to catalytic mechanism and evolution.

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Journal
Communications Chemistry
Published
2026-04-14
DOI
https://doi.org/10.1038/s42004-026-01986-9
Primary Topic
Biochemical and biochemical processes
Type
article
Field-Weighted Citation Impact
0.00

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article

Lid loop-mediated proton transfer revealed in the Fe/αKG-dependent decarboxylase TraH

Shu‐Ming Li, Johannes Freitag, Mathias Girbig, Aitao Li et al.
Communications Chemistry
Biochemical and biochemical processes
article

Lid loop-mediated proton transfer revealed in the Fe/αKG-dependent decarboxylase TraH

Shu‐Ming Li, Johannes Freitag, Mathias Girbig, Aitao Li, Zhiyong Guo, Liujuan Zheng, Georg KA Hochberg, Gert Bange, Xuehua Zheng, Rui Ge
article en

Abstract

TraH, a fungal decarboxylase from Penicillium crustosum, belongs to the isopenicillin N synthase (IPNS) subfamily of non-heme iron/α-ketoglutarate (αKG)-dependent enzymes. IPNS enzymes are characterized by N- and C-terminal insertions that can reshape the active site. However, the functional and mechanistic roles of these elements, particularly in fungal decarboxylases, remain largely unexplored. Here, we report crystal structures of TraH in complex with various substrates, revealing a N-terminal loop, serving as lid and undergoes substrate-dependent dynamic conformational rearrangements. Upon binding of crustosic acid, this lid loop forms a hydrogen-bonding network to stabilize a water molecule, which mediates interaction between the conserved K191 residue in the DSBH (double-stranded β-helix) core and the substrate. Mutagenesis and QM/MM metadynamics simulations suggest that proton transfer from K191 is mediated by water molecules stabilized by the lid loop, supporting a decarboxylation mechanism distinct from the canonical strategy of direct carboxylate stabilization by DBSH core-located basic residues in other αKG-dependent decarboxylases. Interestingly, this loop is dispensable for the desaturation of crustosic acid methyl ester, thereby pinpointing its essential role to the precise positioning of the carboxylate substrate for proton transfer during decarboxylation. Evolutionary and structural analyses reveal significant variation in lid loop composition across IPNS enzymes, indicating its contribution to substrate recognition and functional diversification. Overall, our findings uncover a regulatory element in iron/αKG-dependent enzymes and offer insights into how non-core structural elements contribute to catalytic mechanism and evolution.

Communications ChemistryVol. 9(1)
Philipps University of Marburg (DE), Loewe Center for Synthetic Microbiology (DE), State Key Laboratory of Respiratory Disease (CN), Max Planck Institute for Terrestrial Microbiology (DE), Hubei University (CN), Guangzhou Medical University (CN)
Deutsche Forschungsgemeinschaft, Max-Planck-Gesellschaft, China Scholarship Council
Clean water and sanitation
Openalex Percentile: Top 22%
Biochemical and biochemical processes
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