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dc.contributor.advisorMcGillivray, Shaunaen_US
dc.creatorCaron, Alexander Jacob
dc.date.accessioned2024-05-07T14:08:19Z
dc.date.available2024-05-07T14:08:19Z
dc.date.issued2024-05-06
dc.identifier.urihttps://repository.tcu.edu/handle/116099117/64291
dc.description.abstractZinc oxide nanoparticles (ZnO NPs) are promising antimicrobial agents due to their broad-spectrum antibacterial activity and low production cost. Despite many studies demonstrating the effectiveness of ZnO NPs, the antibacterial mechanism is still unknown. Previous work has implicated the role of reactive oxygen species, physical damage of the cell envelope, and/or release of toxic Zn2+ ions as possible mechanisms of action. Assays utilizing S. aureus mutant strains ¿katA and ¿mprF demonstrated that hydrogen peroxide and electrostatic interactions are not crucial for mediating ZnO NP toxicity. Instead, we find Zn2+ accumulation mediates toxicity independent of physical contact. Through this, we conclude that soluble Zn2+ is the primary mechanism by which ZnO NPs mediate toxicity in Mueller-Hinton Broth. Future work investigating the effect of ZnO NP synthesis methods on Zn2+ dissolution could allow for the synthesis of ZnO NPs that possess chemical and morphological properties best suited for antibacterial efficacy.en_US
dc.format.mediumFormat: Onlineen_US
dc.language.isoenen_US
dc.subjectBiologyen_US
dc.subjectAntimicrobial mechanismsen_US
dc.subjectZinc oxide nanoparticlesen_US
dc.subjectS. aureusen_US
dc.subjectZnO toxicityen_US
dc.titleZinc oxide nanoparticles mediate bacterial toxicity in Mueller-Hinton broth via zn2+en_US
dc.typeTexten_US
etd.degree.levelMaster of Scienceen_US
local.collegeCollege of Science and Engineeringen_US
local.departmentBiology
dc.type.genreThesisen_US


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