Back to Search
Start Over
Enzymatic Catalysis at Nanoscale: Enzyme-Coated Nanoparticles as Colloidal Biocatalysts for Polymerization Reactions
- Source :
- ACS Omega, Vol 2, Iss 10, Pp 7305-7312 (2017), ACS Omega
- Publication Year :
- 2017
- Publisher :
- American Chemical Society, 2017.
-
Abstract
- Enzyme-catalyzed controlled radical polymerization represents a powerful approach for the polymerization of a wide variety of water-soluble monomers. However, in such an enzyme-based polymerization system, the macromolecular catalyst (i.e., enzyme) has to be separated from the polymer product. Here, we present a compelling approach for the separation of the two macromolecular species, by taking the catalyst out of the molecular domain and locating it in the colloidal domain, ensuring quasi-homogeneous catalysis as well as easy separation of precious biocatalysts. We report on gold nanoparticles coated with horseradish peroxidase that can catalyze the polymerization of various monomers (e.g., N-isopropylacrylamide), yielding thermoresponsive polymers. Strikingly, these biocatalyst-coated nanoparticles can be recovered completely and reused in more than three independent polymerization cycles, without significant loss of their catalytic activity.
- Subjects :
- separation
Materials science
enhanced activity
supports
General Chemical Engineering
Radical polymerization
02 engineering and technology
010402 general chemistry
01 natural sciences
Article
Enzyme catalysis
Catalysis
lcsh:Chemistry
chemistry.chemical_compound
Polymer chemistry
Thermoresponsive polymers in chromatography
chemistry.chemical_classification
General Chemistry
Polymer
021001 nanoscience & nanotechnology
horseradish-peroxidase
radical polymerization
0104 chemical sciences
Monomer
Polymerization
Chemical engineering
chemistry
lcsh:QD1-999
Colloidal gold
gold nanoparticles
immobilization
cells
0210 nano-technology
nanorods
Subjects
Details
- Language :
- English
- ISSN :
- 24701343
- Volume :
- 2
- Issue :
- 10
- Database :
- OpenAIRE
- Journal :
- ACS Omega
- Accession number :
- edsair.doi.dedup.....ee4e423566d01d02e40f96386184caaa