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dc.contributor.authorFavero, Fernanda-
dc.contributor.authorTolentino, Terezinha Alves-
dc.contributor.authorFernandes, Vinicius-
dc.contributor.authorTreptow, Werner-
dc.contributor.authorPereira, Alex Leite-
dc.contributor.authorMachado, Angelo Henrique Lira-
dc.date.accessioned2023-11-28T13:14:42Z-
dc.date.available2023-11-28T13:14:42Z-
dc.date.issued2023-06-15-
dc.identifier.citationFAVERO, Fernanda et al. α-Alkylidene δ-lactones inhibit quorum sensing phenotypes in Chromobacterium strain CV026 showing interaction with the CviR receptor. RSC Advances, [S. l.], v. 13, p. 18045-18057, 2023. DOI: https://doi.org/10.1039/D3RA01975F. Disponível em: https://pubs.rsc.org/en/content/articlelanding/2023/ra/d3ra01975f. Acesso em: 27 nov. 2023.pt_BR
dc.identifier.urihttp://repositorio2.unb.br/jspui/handle/10482/46916-
dc.language.isoengpt_BR
dc.publisherThe Royal Society of Chemistrypt_BR
dc.rightsAcesso Abertopt_BR
dc.titleα-Alkylidene δ-lactones inhibit quorum sensing phenotypes in Chromobacterium strain CV026 showing interaction with the CviR receptorpt_BR
dc.typeArtigopt_BR
dc.subject.keywordBactériaspt_BR
dc.subject.keywordLactonaspt_BR
dc.rights.license(CC BY NC) This article is licensed under aCreative Commons Attribution-NonCommercial 3.0 Unported Licence.pt_BR
dc.identifier.doihttps://doi.org/10.1039/D3RA01975Fpt_BR
dc.description.abstract1Disruption of bacterial quorum sensing (QS) is presented as a promising strategy to overcome clinically relevant and phytopathogenic bacteria. This work presents α-alkylidene δ-lactones as new chemical scaffolds that inhibit the biosynthesis of violacein in the biosensor strain Chromobacterium CV026. Three molecules displayed higher than 50% violacein reduction when tested at concentrations lower than 625 µM. The most active α-alkylidene δ-lactone inhibited the hydrolysis of chitin concomitantly with the inhibition of violacein production in CV026, suggesting the disruption of its QS machinery. Further, RT-qPCR and competition experiments showed this molecule to be a transcriptional inhibitor of the QS-regulated operon vioABCDE. Docking calculations suggested a good correlation between binding affinity energies and inhibition effects, with all molecules positioned within the CviR autoinducer-binding domain (AIBD). The most active lactone yielded the best binding affinity energy, most probably due to its unprecedented binding with the AIBD. Our results show α-alkylidene δ-lactones as promising chemical scaffolds for the development of new QS inhibitors affecting LuxR/LuxI-systems.pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0003-4284-9929pt_BR
dc.description.unidadeInstituto de Química (IQ)pt_BR
dc.description.unidadeFaculdade UnB Ceilândia (FCE)pt_BR
dc.description.unidadeInstituto de Ciências Biológicas (IB)pt_BR
dc.description.unidadeDepartamento de Biologia Celular (IB CEL)pt_BR
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