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Effects of Synthetic Tetronamides and Methylated Denigrins on Bacterial Quorum Sensing and Biofilm Formation

Sweta RoyDepartment of Biomedical and Chemical Engineering, Syracuse University, Syracuse, New York 13244, United StatesJaime A. M. AcostaChemical Technology School, Universidad Tecnológica de Pereira, Carrera 27 #10-02, Barrio Álamos, Risaralda, Pereira Código postal 660003, ColombiaMilandip KarakDepartment of Chemistry, Faculty of Science, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, JapanIsabela Ramirez-VelezDepartment of Biomedical and Chemical Engineering, Syracuse University, Syracuse, New York 13244, United StatesKohei TorikaiDepartment of Chemistry, Faculty of Science, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, JapanDacheng RenDepartment of Biomedical and Chemical Engineering and Civil and Environmental Engineering and Biology, Syracuse University, Syracuse, New York 13244, United StatesLuiz C. A. BarbosaDepartment of Chemistry, Universidade Federal de Minas Gerais, Av. Pres. Antônio Carlos, 6627, Campus Pampulha, Belo Horizonte, MG CEP 31270-901, Brazil
ACS Omegajournal2023en
ABI

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Detrimental biofilms of bacterial pathogens cause chronic infections with a high-level tolerance to antibiotics. To identify new control agents, we synthesized and tested a total of 14 tetronamides (including 5 new compounds) and 6 denigrin intermediates on the model species Escherichia coli. At a concentration of 50 μg/mL, two tetronamides and two methylated denigrins exhibited significant inhibitory effects against biofilm formation of E. coli RP437, e.g., by 60 and 94%, respectively. Structural analysis of the tested compounds revealed that p-methoxybenzylidene and p-methoxyphenethyl moieties of denigrins are important for biofilm inhibition, while the former group is also essential to the activity against quorum sensing (QS) via AI-2. Specifically, tetramethyldenigrin B has strong inhibitory effects against both E. coli biofilm formation and AI-2-mediated QS and thus provides a promising lead structure for designing better control agents. Consistently, tetramethyldenigrin B also showed inhibitory activity against biofilm formation of uropathogenic E. coli. Together, these findings provide new insights for the rational design of novel biofilm and QS inhibitors.

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