journal article·2026-04-08Open access

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

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

ACS Applied Materials & Interfaces· Volume 18· Issue 13

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.
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Research context

OpenAlex topics: Enzyme function and inhibition · Metal-Catalyzed Oxygenation Mechanisms · Enzyme Catalysis and Immobilization

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry

National Institute of Technology Warangal

State Key Laboratory of Analytical Chemistry for Life Science, Kuang Yaming Honors School, Chemistry and Biomedicine Innovation Center (ChemBIC), Institute for Brain Sciences

Nanjing University

Indian Institute of Technology (BHU)

School of Plant Sciences and Food Security, The George S. Wise Faculty of Life Sciences

Tel Aviv University

Department of Chemical Research Support

Weizmann Institute of Science

The Shmunis School of Biomedicine and Cancer Research, The George S. Wise Faculty of Life Sciences

Department of Materials Science and Engineering

Funding

European Research Council · Jiangsu Provincial Department of Finance · National Institute of Technology Warangal · Jiangsu Science and Technology Department · National Basic Research Program of China (973 Program) · National Natural Science Foundation of China (NSFC)

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