Answers are grounded in this paper and cite their sources.
Shows improved catalytic efficiency in transaminases, indicating potential for producing chiral compounds.
Transaminases (TAs) play a crucial role in asymmetric synthesis, among which ω-TA exhibits a broad substrate spectrum and high enantioselectivity, albeit with limitations such as poor stability and low enzymatic activity. This study aimed to improve the catalytic efficiency of the rate-limiting transaminase in the cascade reaction for 2-amino-4-hydroxybutyric acid, using strategies such as semirational design and DLKcat large model prediction. After single-point and combinatorial mutations, ultimately, a combinatorial mutant, S62T/T68D/Y221Q (VfTA-M3), with a relative specific activity of 379.42% compared to the wild-type (VfTA-WT), was obtained, which also exhibited improved stability relative to the wild-type enzyme. Using this mutant in conjunction with aldolase RtALD, a cascade catalytic system was established for the synthesis of 2-amino-4-hydroxybutyric acid from inexpensive formaldehyde and pyruvate. After 20 h of reaction, the substrate conversion rate reached 80%, laying a solid foundation for the production of other chiral amino acids and chiral amines.
No takes yet. Share an insight, caveat, or question.
Hong et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: