Angew Chem Int Ed Engl. 2026 Sep 29:e1881662. doi: 10.1002/anie.1881662. Online ahead of print.
ABSTRACT
Azacitidine is a rare triazine-containing nucleoside and a clinically used DNA methyltransferase inhibitor for the treatment of myelodysplastic syndromes. Despite its medical importance, its biosynthetic pathway has remained elusive. Herein, we identified the azacitidine biosynthetic gene cluster (aza BGC) from Streptomyces mobaraensis IPIO2 using a resistance gene-guided comparative genomics strategy and elucidated its biosynthetic pathway via in vivo and in vitro studies. Unexpectedly, the bifunctional GTP cyclohydrolase I AzaE generates the triaminopyrimidine intermediate as the major product and H2NTP as a shunt product from GTP, diverging from canonical GCHI enzymes. The cofactor-independent cupin dioxygenase AzaA then assembles the 1,3,5-triazine scaffold using both O2 and H2O as oxygen donors, a mechanism unprecedented in nucleoside antibiotic biosynthesis. Subsequent decarboxylation by AzaB/AzaC, phosphoribosyl transfer by AzaD, and dephosphorylation by AzaG together with other endogenous hydrolases yield azacitidine. This work uncovers a distinct biosynthetic logic for triazine-containing nucleosides and provides a molecular basis for the synthetic biology-driven production of azacitidine.
PMID:42806946 | DOI:10.1002/anie.1881662