Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/10333
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dc.contributor.authorGuiomar, A. Jorge-
dc.contributor.authorGuthrie, James T.-
dc.contributor.authorEvans, Stephen D.-
dc.date.accessioned2009-06-25T08:13:24Z-
dc.date.available2009-06-25T08:13:24Z-
dc.date.issued1999-02-16-
dc.identifier.citationLangmuir. 15:4 (1999) 1198-1207en_US
dc.identifier.issn0743-7463-
dc.identifier.urihttps://hdl.handle.net/10316/10333-
dc.description.abstractMixed self-assembled monolayers (SAMs) composed of a medium length, reactive, n-organothiol (11-mercaptoundecanoic acid) and a short length, unreactive, hydrophobic n-alkylthiol (7-heptanethiol) chemisorbed onto evaporated gold surfaces, were used to study the effect of the microenvironment on the structure and activity of immobilized glucose oxidase (GOX). The mixed SAMs were characterized by X-ray photoelectron spectroscopy, contact angle measurements, and cyclic voltammetry. The derivatization of the SAMs for the covalent attachment and the immobilized enzyme were studied by X-ray photoelectron spectroscopy. Quantitative analysis of the amide I band of the infrared spectra of GOX immobilized onto surfaces at the two attainable extremes of the hydrophilicity range available to us indicated that the percentage of β sheet increased with increasing hydrophilicity of the microenvironment. The specific activity of GOX was higher when the enzyme was immobilized onto the hydrophobic microenvironment.en_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsopenAccesseng
dc.titleUse of Mixed Self-Assembled Monolayers in a Study of the Effect of the Microenvironment on Immobilized Glucose Oxidaseen_US
dc.typearticleen_US
dc.identifier.doi10.1021/la980974t-
item.openairetypearticle-
item.fulltextCom Texto completo-
item.languageiso639-1en-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
Appears in Collections:FCTUC Ciências da Vida - Artigos em Revistas Internacionais
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