Investigation of immobilized biopolymers for metal binding

dc.contributor.advisorHolcombe, James A.en
dc.creatorMalachowski, Lisa Lynen
dc.date.accessioned2008-08-28T21:52:37Zen
dc.date.available2008-08-28T21:52:37Zen
dc.date.issued2004en
dc.descriptiontexten
dc.description.abstractThis research focuses on the utility of immobilized poly amino acids for metal remediation and preconcentration. The biohomopolymer poly-L-histidine (PLHis) was immobilized onto controlled pore glass (CPG) and its metal binding capabilities evaluated through the use of a flow injection analysis - flame atomic absorption system (FIA-FAAS). The metal binding capability of PLHis-CPG was determined through the analysis of the generated breakthrough curves. The polymer likely coordinates cationic metals through the imidazole side chain (pKa ≈ 6) present on each histidine residue with both strong and weak binding sites for Cu2+, Cd2+, Co2+, and Ni2+. It has also been shown that the protonated imidazole side chain present in acidic conditions is capable of binding metal oxyanions such as chromates, arsenates, and selenites; although oxyanion binding currently exhibits interferences from competing anions in solution, such as sulfate and nitrate. Poly-L-Aspartic Acid (PLAsp) and Poly-L-Glutamic Acid (PLGlu) were also individually immobilized onto controlled pore glass (CPG) and compared using their metal binding capabilities. Elemental combustion analysis was used to yield polymer coverage approximations. Formation constants and site capacities of both polymers for Cd2+ were determined through equilibrium and breakthrough studies. Additionally, the metal selectivity of PLAsp and PLGlu was evaluated when breakthrough curves were run with several metals present in solution at one time. Both polymers exhibited similar binding trends and binding strengths for all of the metals studied. This likely reflects the absence of a predetermined tertiary structure of the polymers on the surface and the relatively high residue-per-metal ratio (~20:1), which places less stringent requirements on the steric hindrance between the side chains and the resultant ìwrappingî of the peptide around the metal. Initial attempts at determining formation constants of PLAsp and PLGlu through competitive binding experiments with either EDTA or oxalate present were unsuccessful due to complications caused by the current immobilization procedure. Therefore, alternate immobilization procedures were investigated utilizing an epoxide linker. These methods eliminate the formation of an amine functionality on the surface. Additionally, a combinatorial approach was used in an attempt to elucidate an optimal copolymer primary structure for successful binding of a target metal. This approach included screening the library for successful binding with micro x-ray fluorescence (MXRF) and obtaining the sequence of the successful copolymer through Edman Degradation. A considerable amount of the metal binding experiments conducted in this research used the analysis of breakthrough curves generated through flow injection-flame atomic absorption spectrometry. Solution flow rate is a critical parameter in breakthrough analysis. Due to the absence of an inexpensive, on-line flow meter for flow injection analysis systems, an electronic flow meter was constructed to measure the flow rate during the FIAAS measurements. Thus, flow rates can be measured while collecting breakthrough data, and continuous monitoring of flow rates is possible.
dc.description.departmentChemistry and Biochemistryen
dc.description.departmentChemistryen
dc.format.mediumelectronicen
dc.identifierb59041754en
dc.identifier.oclc57622433en
dc.identifier.proqst3143306en
dc.identifier.urihttp://hdl.handle.net/2152/1242en
dc.language.isoengen
dc.rightsCopyright is held by the author. Presentation of this material on the Libraries' web site by University Libraries, The University of Texas at Austin was made possible under a limited license grant from the author who has retained all copyrights in the works.en
dc.subject.lcshBiopolymersen
dc.subject.lcshAmino acidsen
dc.subject.lcshChelation therapyen
dc.titleInvestigation of immobilized biopolymers for metal bindingen
dc.type.genreThesisen
thesis.degree.departmentChemistryen
thesis.degree.disciplineChemistryen
thesis.degree.grantorThe University of Texas at Austinen
thesis.degree.levelDoctoralen
thesis.degree.nameDoctor of Philosophyen

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