Acosta, JavierNguyen, KimSpitale, Robert C.Fernández Lucas, Jesús2024-10-222024-10-222021-11Acosta J, Nguyen K, Spitale RC, Fernández-Lucas J. Taylor-made production of pyrimidine nucleoside-5′-monophosphate analogues by highly stabilized mutant uracil phosphoribosyltransferase from Toxoplasma gondii. Bioresource Technology 2021;339:125649. https://doi.org/10.1016/j.biortech.2021.125649.0960-852410.1016/j.biortech.2021.125649https://hdl.handle.net/20.500.14352/109276This work was also supported by grant 5R21MH116415 from National Institutes of Health (NIH)Nowadays, enzymatic synthesis of nucleotides is an efficient and sustainable alternative to chemical methodologies. In this regard, after the biochemical characterization of wild-type and mutant uracil phosphoribosyltransferases from Toxoplasma gondii (TgUPRT, TgUPRT2, and TgUPRT3), TgUPRT2 was selected as the optimal candidate (69.5 IU mg−1, UMP synthesis) for structure-guided immobilization onto Ni2+ chelate (MNiUPRT2) and onto glutaraldehyde-activated microparticles (MGlUPRT2). Among resulting derivatives, MNiUPRT23 (6127 IU g−1biocat; 92% retained activity; 3–5 fold enhanced stability at 50–60 °C) and MGlUPRT2N (3711 IU g−1biocat; 27% retained activity; 8–20 fold enhanced stability at 50–60 °C) displayed the best operability. Moreover, the enzymatic synthesis of different pyrimidine NMPs was performed. Finally, the reusability of both derivatives in 5-FUMP synthesis (MNiUPRT23, 80% retained activity after 7 cycles, 5 min; MGlUPRT2N, 70% retained activity after 10 cycles, 20 min) was carried out at short times.engjournal article1873-2976https://doi.org/10.1016/j.biortech.2021.125649https://www.sciencedirect.com/science/article/pii/S0960852421009901?via%3Dihubrestricted access577.113.3577.15577.260Nucleoside-5′-monophosphatesPhosphoribosyltransferasesStructure-guided immobilizationBioquímica (Biología)Biología molecular (Biología)Biotecnología2403 Bioquímica2415 Biología Molecular2302.09 Enzimología3302 Tecnología Bioquímica2302.23 Ácidos Nucleicos