Going full circle: dynamic covalent enzyme immobilisation via visually trackable boronate esters.

Enzyme immobilisation on solid supports enables biocatalyst recycling but generates significant waste due to single-use resins that are discarded when enzyme activity declines. Here we report a reversible immobilisation strategy based on boronate ester formation between alizarin-functionalised enzymes and boronic acid-modified supports. Alizarin-methyliminodiacetic acid (alizarin-IDA) serves dual roles as both a pH-responsive binding handle and a visual reporter, enabling real-time colourimetric tracking of enzyme loading (red solution → orange resin), immobilisation completeness, and pH-triggered release. A universal labelling protocol was established and successfully applied to four structurally diverse enzymes retaining 77-95% of native activity. All alizarin-labelled enzymes achieved >90% immobilisation yield on different supports, were extensively reusable, and could be removed by acidic treatment with full regeneration of the supports. The load-use-cleave sequence was repeated five times without loss of binding capacity, enabling more than 50 catalytic cycles per support across multiple enzyme lifecycles (5 regeneration cycles × 10+ reactions each) with identical performance.

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Publication Details

Journal
Open Access CRIS of the University of Bern
Published
2026-03-03
DOI
https://doi.org/10.48620/96222
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
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article

Going full circle: dynamic covalent enzyme immobilisation via visually trackable boronate esters.

Glenn Bojanov, Francesca Paradisi, Juliette Swit
Open Access CRIS of the University of Bern
Enzyme Catalysis and Immobilization
article

Going full circle: dynamic covalent enzyme immobilisation via visually trackable boronate esters.

Glenn Bojanov, Francesca Paradisi, Juliette Swit
article en

Abstract

Enzyme immobilisation on solid supports enables biocatalyst recycling but generates significant waste due to single-use resins that are discarded when enzyme activity declines. Here we report a reversible immobilisation strategy based on boronate ester formation between alizarin-functionalised enzymes and boronic acid-modified supports. Alizarin-methyliminodiacetic acid (alizarin-IDA) serves dual roles as both a pH-responsive binding handle and a visual reporter, enabling real-time colourimetric tracking of enzyme loading (red solution → orange resin), immobilisation completeness, and pH-triggered release. A universal labelling protocol was established and successfully applied to four structurally diverse enzymes retaining 77-95% of native activity. All alizarin-labelled enzymes achieved >90% immobilisation yield on different supports, were extensively reusable, and could be removed by acidic treatment with full regeneration of the supports. The load-use-cleave sequence was repeated five times without loss of binding capacity, enabling more than 50 catalytic cycles per support across multiple enzyme lifecycles (5 regeneration cycles × 10+ reactions each) with identical performance.

Open Access CRIS of the University of Bern
Centro Universitário do Pará (BR), Pharmaceutical Biotechnology (Czechia) (CZ)
Responsible consumption and production
Openalex Percentile: Top 15%
Enzyme Catalysis and Immobilization
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