# Engineering polyethylenimine–metal functionalized cryogels for superior catalase binding, activity, and long-term durability

**Authors:** Kadir Erol, Mehmet Hüseyin Alkan, İhsan Alacabey

PMC · DOI: 10.1038/s41598-026-38040-6 · Scientific Reports · 2026-02-09

## TL;DR

Researchers developed a new cryogel material that effectively binds and stabilizes catalase, making it suitable for long-term industrial and environmental uses.

## Contribution

A novel Cu(II)-functionalized cryogel with enhanced catalase immobilization and durability was created.

## Key findings

- The Cu(II)-functionalized cryogel achieved the highest enzyme loading of 391.9 mg·g⁻¹.
- Immobilized catalase showed a 2.8-fold increase in kcat/Km and improved thermal and storage stability.
- The cryogel retained 34.2% activity after 15 operational cycles.

## Abstract

Cryogels with interconnected macroporous architectures offer significant advantages as enzyme immobilization supports due to their high permeability, mechanical robustness, and tunable surface chemistry. In this study, a novel Poly(HEMA-co-GMA) cryogel was synthesized and subsequently modified through polyethyleneimine (PEI) grafting and transition-metal chelation to create high-affinity matrices for catalase immobilization. Among the metal ions tested with Cu(II), Ni(II), and Co(II), the Cu(II)-functionalized cryogel exhibited superior physicochemical properties, including the highest water retention capacity (438.4%), well-preserved porosity, and strong coordination interactions with amine-rich PEI domains. FT-IR, SEM, TGA, BET, elemental analysis, and ICP-OES results confirmed successful stepwise modification and metal loading. Catalase immobilization studies revealed that the Poly(HEMA-co-GMA)-PEI-Cu(II) cryogel achieved the highest enzyme loading (391.9 mg·g⁻¹), with an optimal immobilization time of 8 h and optimum pH near neutrality. Kinetic analysis demonstrated a substantial decrease in Km (from 57.3 to 14.4 mM), indicating enhanced substrate affinity, while kcat/Km increased 2.8-fold relative to the free enzyme. The immobilized catalase exhibited improved thermal tolerance, strong operational stability (34.2% activity after 15 cycles), high desorption efficiency (96% in the first cycle), and markedly superior storage stability (62.1% activity after 70 days at 4 °C) compared to its free counterpart. These results validate the Cu(II)-chelated Poly(HEMA-co-GMA)-PEI cryogel as a highly efficient and reusable biocatalytic platform with significant potential for industrial and environmental enzyme-based applications.

## Linked entities

- **Proteins:** Cat (Catalase)
- **Chemicals:** Cu(II) (PubChem CID 27099), Ni(II) (PubChem CID 934), Co(II) (PubChem CID 104729), PEI (PubChem CID 9033)

## Full-text entities

- **Genes:** CAT (catalase) [NCBI Gene 847]
- **Chemicals:** metal (MESH:D008670), polyethylenimine (MESH:D011094)

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12953862