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Pestic Biochem Physiol ; 202: 105967, 2024 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-38879344

RESUMEN

Coumarin is a natural product known for its diverse biological activities. While its antifungal properties in agricultural chemistry have been extensively studied, there is limited research on its antibacterial potential. In this study, we developed several novel coumarin derivatives by combining coumarin with pyridinium salt through molecular hybridization and chemical synthesis. Our findings reveal that most of these derivatives exhibit promising antibacterial activity. Among them, derivative A25 has been identified as the most effective compound based on three-dimensional quantitative structure-activity relationships. It demonstrates significant in vitro and in vivo activity against Xanthomonas oryzae pv. oryzae (Xoo), Xanthomonas oryzae pv. oryzicola (Xoc), and Xanthomonas campestris pv. citri (Xac), outperforming the commercially available thiediazole copper. Initial investigations into its mechanism of action suggest that A25 disrupts the cell membranes of Xoc and Xoo, thereby inhibiting bacterial growth. Additionally, A25 enhances the activity of defense enzymes in rice and modulates the expression of proteins related to the pyruvate metabolism pathway. This dual action contributes to rice's resistance against bacterial infestation. We anticipate that this study will serve as a foundation for the development of coumarin-based bactericides.


Asunto(s)
Antibacterianos , Cumarinas , Pruebas de Sensibilidad Microbiana , Oryza , Xanthomonas , Cumarinas/farmacología , Cumarinas/síntesis química , Cumarinas/química , Antibacterianos/farmacología , Antibacterianos/síntesis química , Antibacterianos/química , Xanthomonas/efectos de los fármacos , Oryza/microbiología , Compuestos de Piridinio/farmacología , Compuestos de Piridinio/química , Compuestos de Piridinio/síntesis química , Xanthomonas campestris/efectos de los fármacos , Diseño de Fármacos , Sales (Química)/farmacología , Sales (Química)/química , Relación Estructura-Actividad
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