Demonstrates improved enzyme activity in continuous-flow biocatalysis, implying a sustainable method for fine chemical production.
High Resolution Image Download MS PowerPoint Slide Biocatalysis has proved to be of great importance to pursue a more sustainable production of fine chemicals, and enzyme immobilization is a crucial tool to achieve this goal. In this work, hydroxyapatite, an eco-friendly material, was used as a support for the immobilization of a γ-glutamyltransferase from Escherichia coli, an enzyme that catalyzes the synthesis of bioactive γ-glutamyl derivatives, exploiting the noncovalent interactions between the support and the enzyme. After screening the immobilization conditions, the storage (up to 90 days) and the thermal stability (50 °C) of the obtained immobilized biocatalyst were studied, as well as its reuse in up to 10 consecutive reactions of γ-glutamylation of S -allyl- l -cysteine, to give γ- l -glutamyl- S -allyl- l -cysteine ( 3 ), a flavor enhancer occurring in garlic extract. Finally, the immobilized enzyme was used to prepare a packed-bed reactor and 3 was synthesized under continuous-flow conditions improving both the productivity (from 19.4 to 35.1 μmol·h –1 ) and the space-time yield (9.7 vs 381 μmol·h –1 ·mL –1 ) of the reaction.
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Gelati et al. (2026) studied this question.
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