Demonstrates enhanced O2 transport and H2O2 resistance in dioxygenases, suggesting a novel engineering approach.
Fe(II)/α‐ketoglutarate‐dependent dioxygenases (αKGDs) are versatile biocatalysts whose catalytic activity relies on an efficient supply of O 2 and αKG. However, in engineering applications, the O 2 supply is seldom considered, whereas αKG is typically supplied through the oxidation of l ‐glutamate by l ‐glutamate oxidase, which concomitantly produces H 2 O 2 that potently inhibits αKGD activity. This study developed a tunnel engineering strategy based on random accelerated molecular dynamics and protein structuromics to precisely modulate the access of small molecules (O 2 and H 2 O 2 ) to isoleucine dioxygenase (IDO), enhancing O 2 transport while resisting H 2 O 2 transport. Notably, mutant 1 (L179C/V225F/I240V) and mutant 2 (N193S/V225I/I240V) displayed markedly higher catalytic activity for five aliphatic amino acid substrates (Leu, Nle, Nva, Met, and Ile), reaching 27.2‐fold greater activity. In addition, mutant 2 exhibited 7.1‐fold higher activity against Ile in the presence of H 2 O 2 . This study highlights O 2 and H 2 O 2 tunnel engineering as a new strategy for enhancing αKGDs activity and antioxidative properties.
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Liu et al. (2026) studied this question.
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