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Please use this identifier to cite or link to this item: http://arks.princeton.edu/ark:/88435/dsp01hm50tw00h
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dc.contributor.advisorLink, A. James-
dc.contributor.authorGallagher, Kelly-
dc.date.accessioned2023-07-21T17:42:40Z-
dc.date.available2023-07-21T17:42:40Z-
dc.date.created2023-04-24-
dc.date.issued2023-07-21-
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/dsp01hm50tw00h-
dc.description.abstractBiodegradation of polyethylene terephthalate (PET), which is the basis for many consumer plastics, has been an area of great interest recently with regards to plastic recycling. Several bacterial enzymes have been discovered that have low-level PET degradation activity. However, this activity must be increased and enzyme functionality at higher temperatures must be achieved before biodegradation techniques can become impactfully utilized for environmental plastic biodegradation. Using machine learning predictions and sequence alignments in the design process, amino acid mutagenesis was performed on the cutinase from Thermobifida fusca. Activity was analyzed through degradation assays with a BHET substrate, and two promising mutants, pKG2 and pKG3, were observed to have significant activity at 70 °C.en_US
dc.format.mimetypeapplication/pdf
dc.language.isoenen_US
dc.titleDevelopment of Stabilized Thermobifida fusca Cutinases for Improved PET Degradationen_US
dc.typePrinceton University Senior Theses
pu.date.classyear2023en_US
pu.departmentChemical and Biological Engineeringen_US
pu.pdf.coverpageSeniorThesisCoverPage
pu.contributor.authorid920227840
pu.certificateEngineering Biology Programen_US
pu.mudd.walkinNoen_US
Appears in Collections:Chemical and Biological Engineering, 1931-2023

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