Exploring Siderophore-Mineral Interaction Using Force Microscopy and Computational Chemistry

dc.contributor.authorKendall, Treavor Allenen
dc.contributor.committeechairHochella, Michael F. Jr.en
dc.contributor.committeememberHersman, Larryen
dc.contributor.committeememberTadanier, Christopher J.en
dc.contributor.committeememberPotts, Malcolmen
dc.contributor.committeememberRimstidt, J. Donalden
dc.contributor.departmentGeological Sciencesen
dc.date.accessioned2014-03-14T20:09:56Zen
dc.date.adate2003-04-21en
dc.date.available2014-03-14T20:09:56Zen
dc.date.issued2003-04-11en
dc.date.rdate2004-04-21en
dc.date.sdate2003-04-18en
dc.description.abstractThe forces of interaction were measured between the siderophore azotobactin and the minerals goethite (FeOOH) and diaspore (AlOOH) in solution using force microscopy. Azotobactin was covalently linked to a hydrazide terminated atomic force microscope tip using a standard protein coupling technique. Upon contact with each mineral surface, the adhesion force between azotobactin and goethite was two to three times the value observed for the isostructural Al-equivalent diaspore. The affinity for the solid iron oxide surface reflected in the force measurements correlates with the specificity of azotobactin for aqueous ferric iron. Further, the adhesion force between azotobactin and goethite significantly decreases when small amounts of soluble iron are added to the system suggesting a significant specific interaction between the azotobactin and the mineral surface. Changes in the force signature with pH and ionic strength were fairly predictable when considering mineral solubility, the charge character of the mineral surfaces, the molecular structure of azotobactin, and the intervening solution. Molecular and quantum mechanical calculations which were completed to further investigate the interaction between azotobactin and iron/aluminum oxide surfaces, and to more fully understand the force measurements, also showed an increased force affinity for Fe over Al. Ab initio calculations on siderophore fragment analogs suggest the iron affinity can be attributed to increased electron density associated with the Fe-O bond compared to the Al-O bond; an observation that correlates with iron's larger electronegativity compared to aluminum. Attachment of the ligand to each surface was directed by steric forces within the molecule and coulombic interactions between the siderophore oxygens and the metals in the mineral. Chelating ligand pairs coordinated with neighboring metal atoms in a bidentate, binuclear geometry. Upon simulated retraction of azotobactin from each surface, the Fe-O(siderophore) bonds persisted into a higher force regime than Al-O(siderophore) bonds, and surface metals were removed from both minerals. Extrapolation of the model to more realistic hydrated conditions using a PCM model in the quantum mechanical calculations and water clusters in the molecular mechanical model demonstrated that the presence of water energetically favors and enhances metal extraction, making this a real possibility in a natural system.en
dc.description.degreePh. D.en
dc.identifier.otheretd-04182003-134826en
dc.identifier.sourceurlhttp://scholar.lib.vt.edu/theses/available/etd-04182003-134826/en
dc.identifier.urihttp://hdl.handle.net/10919/26961en
dc.publisherVirginia Techen
dc.relation.haspartKendallDissertationETD.pdfen
dc.rightsIn Copyrighten
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/en
dc.subjectdiasporeen
dc.subjectliganden
dc.subjectazotobactinen
dc.subjectmolecular modelingen
dc.subjectquantum mechanical calculationsen
dc.subjectAFMen
dc.subjectgoethiteen
dc.titleExploring Siderophore-Mineral Interaction Using Force Microscopy and Computational Chemistryen
dc.typeDissertationen
thesis.degree.disciplineGeological Sciencesen
thesis.degree.grantorVirginia Polytechnic Institute and State Universityen
thesis.degree.leveldoctoralen
thesis.degree.namePh. D.en

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