Literature DB >> 32262736

Co-immobilization of enzymes with the help of a dendronized polymer and mesoporous silica nanoparticles.

Hanna Gustafsson1, Andreas Küchler, Krister Holmberg, Peter Walde.   

Abstract

The two enzymes Aspergillus sp. glucose oxidase (GOD) and horseradish peroxidase (HRP) were co-immobilized on solid silica supports in a spatially controlled way by using mesoporous silica nanoparticles (Hiroshima Mesoporous Materials, HMM) and a polycationic dendronized polymer (denpol). The silica support was first coated with the denpol, followed by the deposition of the mesoporous silica nanoparticles into which - in a next step - GOD was adsorbed. Finally, the GOD-loaded silica nanoparticles were coated with a denpol-HRP conjugate constituting of several HRP molecules which were covalently bound to the denpol via bis-aryl hydrazone (BAH) bonds. The entire immobilization process was followed in real time with quartz crystal microbalance with dissipation monitoring (QCM-D). The activities and storage stabilities of the co-immobilized enzymes were determined by analyzing a two-step cascade reaction involving the two immobilized enzymes GOD and HRP. d-glucose and o-phenylenediamine (OPD) were used as substrates for GOD and HRP, respectively. The cascade reaction - in which intermediate hydrogen peroxide was formed from d-glucose and dissolved O2 with GOD - was shown to take place. The immobilized enzymes remained fairly stable for at least 2 weeks if stored in contact with an aqueous solution of pH = 7 at 4 °C. If, however, denpol-BAH-GOD coated HRP-loaded mesoporous silica nanoparticles were used (the reversed situation), the cascade reaction was not effective. This was probably due to slow diffusion of hydrogen peroxide from the surface-exposed GOD to the particle-trapped HRP, and/or due to an inefficient loading of active HRP inside the particles. Overall, the combination of two enzyme immobilization methodologies - enzymes adsorbed within mesoporous silica nanoparticles and enzymes adsorbed as denpol-BAH-enzyme conjugates - allows the spatially controlled localization of different types of enzymes in a simple way. Possible applications of the concept are in the field of bioelectrode fabrication.

Entities:  

Year:  2015        PMID: 32262736     DOI: 10.1039/c5tb00543d

Source DB:  PubMed          Journal:  J Mater Chem B        ISSN: 2050-750X            Impact factor:   6.331


  5 in total

1.  Random and Positional Immobilization of Multi-enzyme Systems.

Authors:  Hassan Maleki; Kamyar Khoshnevisan; Hadi Baharifar
Journal:  Methods Mol Biol       Date:  2022

2.  The Impact of Glucose Oxidase Immobilization on Dendritic Gold Nanostructures on the Performance of Glucose Biosensors.

Authors:  Laura Sakalauskiene; Anton Popov; Asta Kausaite-Minkstimiene; Arunas Ramanavicius; Almira Ramanaviciene
Journal:  Biosensors (Basel)       Date:  2022-05-10

3.  Controllable Enzyme Immobilization via Simple and Quantitative Adsorption of Dendronized Polymer-Enzyme Conjugates Inside a Silica Monolith for Enzymatic Flow-Through Reactor Applications.

Authors:  Nicolas Ghéczy; Weina Xu; Katarzyna Szymańska; Andrzej B Jarzębski; Peter Walde
Journal:  ACS Omega       Date:  2022-07-21

4.  A Nanoconfined Four-Enzyme Cascade Simultaneously Driven by Electrical and Chemical Energy, with Built-in Rapid, Confocal Recycling of NADP(H) and ATP.

Authors:  Clare F Megarity; Thomas R I Weald; Rachel S Heath; Nicholas J Turner; Fraser A Armstrong
Journal:  ACS Catal       Date:  2022-07-08       Impact factor: 13.700

5.  Large Changes in Protonation of Weak Polyelectrolyte Brushes with Salt Concentration-Implications for Protein Immobilization.

Authors:  Gustav Ferrand-Drake Del Castillo; Rebekah L N Hailes; Andreas Dahlin
Journal:  J Phys Chem Lett       Date:  2020-06-18       Impact factor: 6.475

  5 in total

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