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dc.contributor.advisorWild, James R.
dc.creatorRudé, Malcolm
dc.date.accessioned2022-04-01T14:05:37Z
dc.date.available2022-04-01T14:05:37Z
dc.date.issued1993
dc.identifier.urihttps://hdl.handle.net/1969.1/CAPSTONE-RudeM_1993
dc.descriptionProgram year: 1992/1993en
dc.descriptionDigitized from print original stored in HDRen
dc.description.abstractE. coli cells expressing a recombinant organophosphate degrading gene (opd) were successfully encapsulated in polyvinyl alcohol (PVA) using cryoimmobilization. Gel matrices were composed of 10% cells in 10% PVA, and electron microscopy demonstrated that the cells were well distributed throughout the gel and that their morphology was preserved. The beads were measured for activity with paraoxon, as a substrate, over a pH range of 4.0-10.0. Thermal stability was assayed by exposing beads to temperatures between 22 and 60°C, and for bioreactor simulation, a column of encapsulated cells was prepared and cheked for performance. Cryoimmobilization proved to be an effective technique for bioremediation.en
dc.format.extent14 pagesen
dc.format.mediumelectronicen
dc.format.mimetypeapplication/pdf
dc.subjectE. colien
dc.subjectorganophosphate degrading geneen
dc.subjectcryoimmobilizationen
dc.subjectbioremediationen
dc.titleBioremediation Of Organophosphate Neurotoxins Using Cryoimmobillzed Matriciesen
dc.title.alternativeBioremediation of Organophosphate Neurotoxins Using Cryoimmobillzed Matriciesen
dc.typeThesisen
thesis.degree.departmentBiochemistry and Biophysicsen
thesis.degree.grantorUniversity Undergraduate Fellowen
thesis.degree.levelUndergraduateen
dc.type.materialtexten


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