Identification of polyketide inhibitors targeting 3-dehydroquinate dehydratase in the shikimate pathway of Enterococcus faecalis
Metadatos
Mostrar el registro completo del ítemAutor
Cheung, Vivian W.N.; Xue, Bo; Hernandez-Valladares, Maria; Go, Maybelle K.; Tung, Alvin; Aguda, Adeleke H.; Robinson, Robert C.; Yew, Wen S.Editorial
Plos One
Fecha
2014-07-29Referencia bibliográfica
Cheung VWN, Xue B, Hernandez-Valladares M, Go MK, Tung A, et al. (2014) Identification of Polyketide Inhibitors Targeting 3-Dehydroquinate Dehydratase in the Shikimate Pathway of Enterococcus faecalis. PLoS ONE 9(7): e103598. doi:10.1371/journal.pone.0103598
Patrocinador
Ministry of Education; National Medical Research Council; National Research Foundation of Singapore; Biomedical Research CouncilResumen
Due to the emergence of resistance toward current antibiotics, there is a pressing need to develop the next generation of antibiotics as therapeutics against infectious and opportunistic diseases of microbial origins. The shikimate pathway is exclusive to microbes, plants and fungi, and hence is an attractive and logical target for development of antimicrobial therapeutics. The Gram-positive commensal microbe, Enterococcus faecalis, is a major human pathogen associated with nosocomial infections and resistance to vancomycin, the "drug of last resort". Here, we report the identification of several polyketide-based inhibitors against the E. faecalis shikimate pathway enzyme, 3-dehydroquinate dehydratase (DHQase). In particular, marein, a flavonoid polyketide, both inhibited DHQase and retarded the growth of Enterococcus faecalis. The purification, crystallization and structural resolution of recombinant DHQase from E. faecalis (at 2.2 Å resolution) are also reported. This study provides a route in the development of polyketide-based antimicrobial inhibitors targeting the shikimate pathway of the human pathogen E. faecalis.





