CO 2 Conversion by a Metal-Coordinated Single Amino Acid Carbonic Anhydrase Enzyme Mimic

Read full text
Authors: Adithya Ramesh, Xiaoyu Wang, Subrat Vishwakarma, Oren Ben-Zvi, Linda J. W. Shimon, Sigal Rencus-Lazar, Pandeeswar Makam, Hao Dong, Ehud Gazit, Om Shanker Tiwari, Brian A. Rosen
Cited by: 2
References: 63

Abstract

High Resolution Image Download MS PowerPoint Slide The rising atmospheric concentration of carbon dioxide (CO 2 ) is assumed to be a key factor in global climate change, requiring robust and sustainable carbon conversion technologies. While carbonic anhydrase (CA) is a highly efficient enzyme for CO 2 sequestration, its industrial application is limited by stability, cost, and scalability challenges. To address these limitations, we developed a CA-mimetic metal-amino acid (Phe-Zn(II)) bionanozyme featuring amyloid-like supramolecular cross-β-sheet architecture that provides high structural stability and recyclability. Gas chromatography (GC) analysis of a continuous flow bubble reactor charged with Phe-Zn(II) bionanozyme exhibits a CO 2 conversion efficiency of approximately 18% in an aqueous medium (pH 7.0, 25 °C, ambient pressure), while maintaining remarkable structural integrity as confirmed by postcatalysis PXRD analysis. The amyloid-like supramolecular cross-β-sheet architecture, stabilized by π-π stacking and intermolecular hydrogen bonding, generates a confined catalytic microenvironment that enhances Zn(II) Lewis’s acidity and promotes efficient CO 2 hydration, which is crucial compared to previous reports. Next, density functional theory (DFT) calculations reveal a three-step catalytic pathway involving hydroxide ion generation, nucleophilic attack, and carbonic acid formation, with a rate-determining barrier of 12.3 kcal/mol, making the reaction feasible at room temperature. We also investigated the impact of different amino acids coordinated with Zn, finding that Phe-Zn(II) shows higher catalytic activity. This is due to the stronger electron-withdrawing effect of the phenyl group, which enhances the Lewis acidity of Zn 2+, activates the Zn 2+ –OH 2 bond, and lowers the rate-determining barrier. Taken together, the combination of experimental catalysis, structural robustness, and mechanistic validation highlights Phe-Zn(II) as a promising, cost-effective, and minimalistic catalyst yet efficient carbonic anhydrase mimic for CO 2 conversion, paving the way for scalable and sustainable carbon sequestration strategies critical for mitigating climate change.

Fields of Study & Subjects

Enzyme function and inhibition Metal-Catalyzed Oxygenation Mechanisms Enzyme Catalysis and Immobilization

Publication details

Journal / source
ACS Applied Materials & Interfaces
Publisher
American Chemical Society (ACS)
Volume
18
Issue
13
Pages
18884–18897
Publication date
26 March 2026
Language
EN