A novel method for quantifying enzyme immobilization in porous carriers using simple NMR relaxometry
M. Raquel Serial (Hamburg University of Technology, TU Delft - Multi Phase Systems)
Luca Schmidt (Hamburg University of Technology)
Muhammad Adrian (Hamburg University of Technology)
Grit Brauckmann (Hamburg University of Technology)
Stefan Benders (Hamburg University of Technology)
Victoria Bueschler (Hamburg University of Technology)
Andreas Liese (Hamburg University of Technology)
Alexander Penn (Hamburg University of Technology)
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Abstract
Enzyme immobilization plays a crucial role in enhancing the stability and recyclability of enzymes for industrial applications. However, traditional methods for quantifying enzyme loading within porous carriers are limited by time-consuming workflows, cumulative errors, and the inability to probe enzymes adsorbed inside the pores. In this study, we introduce Time-Domain Nuclear Magnetic Resonance (TD-NMR) relaxometry as a novel, non-invasive technique for directly quantifying enzyme adsorption within porous carriers. Focusing on epoxy methyl acrylate carriers, commonly used in biocatalysis, we correlate changes in T2 relaxation times with enzyme concentration, leading to the development of an NMR-based pore-filling ratio that quantifies enzyme loading. Validation experiments demonstrate that TD-NMR-derived adsorption curves align closely with traditional photometric measurements, offering a reliable and reproducible alternative for enzyme quantification. The accessibility of tabletop TD-NMR spectrometers makes this technique a practical and cost-effective tool for optimizing biocatalytic processes. Furthermore, the method holds promise for real-time monitoring of adsorption dynamics and could be adapted for a wider range of carrier materials and enzymes.
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