Feedback mode SECM study of laccase and bilirubin oxidase immobilised in a sol–gel processed silicate film
Исследование в режиме обратной связи SECM лакказы и билирубиноксидазы, иммобилизованных в силикатной пленке, полученной методом сол–гел
2010-01-01
SCID: 54.1/fb5p7cek
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bilirubin oxidasefeedback modelaccasescanning electrochemical microscopysol–gel silicate film
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Abstract (AI)
Thin silicate films with immobilised enzymes catalysing dioxygen reduction, i.e. laccase and bilirubin oxidase (BOD), were deposited on glass and poly(methyl 2-methylpropenoate) (Plexiglas) surfaces in a sol-gel process by sol drop evaporation. Scanning electrochemical microscopy (SECM) images and approach curves were recorded using hexacyanoferrate(iii) as mediator in the feedback mode. Confocal laser scanning microscopy (CLSM) images in the reflection mode showed larger film thickness close to the edge of the film and laccase aggregates within the film. SECM images obtained using different dioxygen concentrations showed that the film edge and laccase aggregates exhibit higher enzymatic activity towards dioxygen reduction. SECM current-distance curves enabled the determination of kinetic information at the particular regions of the samples after numerical fitting of model parameters. The heterogeneous first order rate constant at the film border was estimated to be ca. 19 times higher than the value obtained when approaching to the centre of the film. The reason of higher laccase surface concentration at the film edge is carefully discussed. For comparison of laccase and BOD activities, silicate spots of 50 microm diameter were deposited on a single Plexiglas sample and examined using SECM. BOD exhibits much higher activity especially at neutral pH.
Key Findings
1
Confocal laser scanning microscopy (reflection mode) revealed larger film thickness near film edges and presence of laccase aggregates within the film.
2
Direct comparison on 50 μm silicate spots showed BOD has much higher dioxygen-reduction activity than laccase, particularly at neutral pH.
3
SECM current-distance curves fitted to numerical models allowed extraction of local kinetic parameters, yielding a heterogeneous first-order rate constant at the film border ~19 times higher than at the film centre.
4
SECM images across varying O2 concentrations showed film edges and laccase aggregates have higher enzymatic activity for dioxygen reduction than film centers.
5
Thin sol–gel silicate films with immobilised laccase and bilirubin oxidase (BOD) were successfully deposited on glass and Plexiglas by sol drop evaporation.
Research Object
Thin sol–gel processed silicate films with immobilised enzymes (laccase and bilirubin oxidase) deposited on glass and Plexiglas surfaces
Research Subject
Spatially resolved enzymatic activity for dioxygen reduction (including edge vs centre and aggregate regions), and associated heterogeneous first-order kinetics determined by feedback-mode SECM and kinetic model fitting
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2010-01-01
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