Synthesis of Unnatural Dipeptides Against Pseudomonas Aeruginosa

dc.contributor.advisorMudrack, Dr. Kristen
dc.contributor.authorRodgers, Hannah
dc.contributor.authorBlanton, Madison
dc.date.accessioned2020-04-28T14:47:47Z
dc.date.available2020-04-28T14:47:47Z
dc.date.issued2020
dc.description.abstractPseudomonas aeruginosa is a bacteria prominent in the lungs of patients with Cystic Fibrosis. The current antibiotics against it are becoming less effective due to the rise in antibiotic resistant strains of P. aeruginosa . As a result, there has been an urgent need to revise the production of antibiotics against this bacteria, and this improvement has come with the production of unnatural dipeptides. In this project, the amino acids used were either alanine, valine, or D-valine with 2 or 3 -fluorophenylalanine as the second amino acid group. The biofilm assay results indicated that 3-fluorophenylalanine with D-valine was the most effective combination against P. aeruginosa, which adds to the results of previous researchers, Andi Lamb and Kellee Geren. Continued research is needed in the future to ensure significance.en_US
dc.identifier.urihttp://hdl.handle.net/11558/5077
dc.language.isoen_USen_US
dc.subjectCystic Fibrosisen_US
dc.subjectPseudomonas aeruginosaen_US
dc.subjectUV Visen_US
dc.subjectAntibioticsen_US
dc.subjectAntibiotic resistanceen_US
dc.subjectDipeptidesen_US
dc.subjectBiofilmen_US
dc.subjectBiofilm assayen_US
dc.subjectRISE Above Research Conference
dc.subjectRISE Above Research Conference
dc.titleSynthesis of Unnatural Dipeptides Against Pseudomonas Aeruginosaen_US
dc.typeWorking Paperen_US

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