Dynemicin A Derivatives as Potential Cancer Chemotherapeutics by Mutasynthesis.

ABSTRACT: The enediyne antitumor antibiotics have remarkable structures and exhibit potent DNA cleavage properties that have inspired continued interest as cancer therapeutics. Their complex structures and high reactivity, however, pose formidable challenges to their production and development in the clinic. We report here proof-of-concept studies using a mutasynthesis strategy to combine chemical synthesis of select modifications to a key iodoanthracene-γ-thiolactone intermediate in the biosynthesis of dynemicin A and all other known anthraquinone-fused enediynes (AFEs). By chemical complementation of a mutant bacterial producer that is incapable of synthesizing this essential building block, we show that derivatives of dynemicin can be prepared substituted in the A-ring of the anthraquinone motif.

SUBMITTER: Pal P 

PROVIDER: S-EPMC11415272 | biostudies-literature | 2023 Dec

REPOSITORIES: biostudies-literature