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Targeted Genome Mining Reveals the Biosynthetic Gene Clusters of Natural Product CYP51 Inhibitors.
Liu, Nicholas; Abramyan, Elizabeth D; Cheng, Wei; Perlatti, Bruno; Harvey, Colin J B; Bills, Gerald F; Tang, Yi.
Affiliation
  • Perlatti B; Texas Therapeutics Institute, The Brown Foundation Institute of Molecular Medicine, The University of Texas Health Science Center at Houston, Houston, Texas 77054, United States.
  • Harvey CJB; Hexagon Bio, Menlo Park, California 94025, United States.
  • Bills GF; Texas Therapeutics Institute, The Brown Foundation Institute of Molecular Medicine, The University of Texas Health Science Center at Houston, Houston, Texas 77054, United States.
J Am Chem Soc ; 143(16): 6043-6047, 2021 04 28.
Article de En | MEDLINE | ID: mdl-33857369
ABSTRACT
Lanosterol 14α-demethylase (CYP51) is an important target in the development of antifungal drugs. The fungal-derived restricticin 1 and related molecules are the only examples of natural products that inhibit CYP51. Here, using colocalizations of genes encoding self-resistant CYP51 as the query, we identified and validated the biosynthetic gene cluster (BGC) of 1. Additional genome mining of related BGCs with CYP51 led to production of the related lanomycin 2. The pathways for both 1 and 2 were identified from fungi not known to produce these compounds, highlighting the promise of the self-resistance enzyme (SRE) guided approach to bioactive natural product discovery.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Produits biologiques / Inhibiteurs de la 14-alpha déméthylase / Famille-51 de cytochromes P450 Langue: En Journal: J Am Chem Soc Année: 2021 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Produits biologiques / Inhibiteurs de la 14-alpha déméthylase / Famille-51 de cytochromes P450 Langue: En Journal: J Am Chem Soc Année: 2021 Type de document: Article