Download MendeleyStructural study on human microbiome-derived polyketide synthases that assemble genotoxic colibactin.
Kim, M., Kim, J., Lee, G.S., Olinares, P.D.B., Airan, Y., Chow, J.L., Park, J., Jeong, Y., Park, J., Chait, B.T., Herzon, S.B., Kim, C.S., Kang, J.Y.(2025) Structure
- PubMed: 40381618
- DOI: https://doi.org/10.1016/j.str.2025.04.017
- Primary Citation of Related Structures:
8XBL, 8XJT, 8XJU, 8XJY, 8XJZ - PubMed Abstract:
Colibactin, a human microbiome-derived genotoxin, promotes colorectal cancer by damaging the host gut epithelial genomes. While colibactin is synthesized via a hybrid non-ribosomal peptide synthetase (NRPS)-polyketide synthase (PKS) pathway, known as pks or clb, the structural details of its biosynthetic enzymes remain limited, hindering our understanding of its biosynthesis and clinical application. In this study, we report the cryo-EM structures of two colibactin-producing PKS enzymes, ClbC and ClbI, captured in different reaction states using a substrate-mimic crosslinker. Our structural analysis revealed the binding sites of carrier protein (CP) domains of the ClbC and ClbI on their ketosynthase (KS) domains. Further, we identified a novel NRPS-PKS docking interaction between ClbI and its upstream enzyme, ClbH, mediated by the C-terminal peptide ClbH and the dimeric interface of ClbI, establishing a 1:2 stoichiometry. These findings advance our understanding of colibactin assembly line and provide broader insights into NRPS-PKS natural product biosynthesis mechanisms.
Organizational Affiliation:
Department of Chemistry, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.
