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Catalytic degradation of rhodamine blue and bactericidal action of AgBr and chitosan-doped CuFe 2 O 4 nanostrucutres evidential molecular docking analysis.
- Source :
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International journal of biological macromolecules [Int J Biol Macromol] 2024 Feb; Vol. 258 (Pt 1), pp. 128885. Date of Electronic Publication: 2023 Dec 22. - Publication Year :
- 2024
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Abstract
- The harmful cationic dyes present in industrial waste significantly decrease the effectiveness of remedy operations. Considering the horrendous impact of these dyes on the environment and biodiversity, silver bromide (AgBr) and chitosan (CS) doped copper ferrite (CuFe <subscript>2</subscript> O <subscript>4</subscript> ) nanostructures (NSs) were prepared by the co-precipitation route. In this work, The surface characteristics of CuFe <subscript>2</subscript> O <subscript>4</subscript> can be altered by CS, potentially enhancing its catalytic reaction compatibility. The functional groups in CS interact with the surface of CuFe <subscript>2</subscript> O <subscript>4</subscript> , influencing its catalytic behavior. AgBr can have an impact on the dynamics of charge carriers in the composite. Better charge separation and transfer which is essential for catalytic processes. The catalytic degradation of RhB was significantly enhanced (100 %) using 4 wt% of AgBr-doped CS-CuFe <subscript>2</subscript> O <subscript>4</subscript> catalysts in a basic medium. The significant inhibitory zones (9.25 to 17.95 mm) inhibitory in maximum doses were seen against Gram-positive bacteria (S. aureus). The bactericidal action of AgBr/CS-doped CuFe <subscript>2</subscript> O <subscript>4</subscript> NSs against DNA gyrase <subscript>S.aureus</subscript> and tyrosyl-tRNAsynthetase S. aureus was rationalized using molecular docking studies, which supported their function as inhibitors.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2023. Published by Elsevier B.V.)
Details
- Language :
- English
- ISSN :
- 1879-0003
- Volume :
- 258
- Issue :
- Pt 1
- Database :
- MEDLINE
- Journal :
- International journal of biological macromolecules
- Publication Type :
- Academic Journal
- Accession number :
- 38143064
- Full Text :
- https://doi.org/10.1016/j.ijbiomac.2023.128885