Photobioelectrocatalysis of Intact Photosynthetic Bacteria Exposed to Dinitrophenol
The outstanding metabolic versatility of purple non-sulphur bacteria makes these organisms an ideal candidate for developing photobioelectrochemical systems applicable in contaminated environments. Here, the effects of 2,4 dinitrophenol, a common contaminant, on purple bacteria photobioelectrocataly...
| Autores: | , , , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2023 |
| País: | Brasil |
| Institución: | Universidade Estadual Paulista (UNESP) |
| Repositorio: | Repositório Institucional da UNESP |
| Idioma: | inglés |
| OAI Identifier: | oai:repositorio.unesp.br:11449/249891 |
| Acceso en línea: | http://dx.doi.org/10.1002/celc.202300013 http://hdl.handle.net/11449/249891 |
| Access Level: | acceso abierto |
| Palabra clave: | biosensor nitrophenol photobioelectrochemistry purple bacteria semiartificial photosynthesis |
| Sumario: | The outstanding metabolic versatility of purple non-sulphur bacteria makes these organisms an ideal candidate for developing photobioelectrochemical systems applicable in contaminated environments. Here, the effects of 2,4 dinitrophenol, a common contaminant, on purple bacteria photobioelectrocatalysis were investigated. The aromatic contaminant clearly affects current generation, with an enhanced photocurrent obtained at low dinitrophenol concentrations (0.5–1 μM), while higher values (up to 100 μM) resulted in a gradual decrease of photocurrent. The obtained electrochemical evidence, coupled to spectroscopic studies, allowed verifying the viability of the bacteria cells after exposure to dinitrophenol, and that no alteration of the photosynthetic apparatus was obtained. The results indicate that high dinitrophenol concentrations divert electrons from the extracellular electron pathway to an alternative electron sink. The present results open the door to the possible use of intact bacteria-based photoelectrodes to develop technologies for sustainable biosensors with simultaneous environmental remediation. |
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