Direct enzyme patterning with microcontact printing and the growth of ZnO nanoparticles on the catalytic templates at room temperature
Document Type
Article
Publication Date
10-18-2011
Abstract
Here we developed a microcontact printing (µCP) process to directly pattern enzymes in a single step without the loss of enzyme activity after printing. By modifying the substrate to display aldehyde groups, the direct stamping of urease enables the simultaneous patterning and covalent cross-linking of urease under the reducing agent NaCNBH4, which does not degrade the enzyme activity. Because the enzyme was not treated by the cross-linker prior to the sampling but rather pre-assembled on the surface of the substrate, only the contact areas of the PDMS stamp reacted with the cross-linker on the substrate, minimizing the poisoning of the enzymatic sites. The exposed urease particles on the substrate, free from the cross-linker, were still catalytically active and utilized to grow crystalline ZnO nanoparticles on the enzyme patterns in ambient conditions and in aqueous solution. © The Royal Society of Chemistry.
Identifier
80054993643 (Scopus)
Publication Title
Journal of Materials Chemistry
External Full Text Location
https://doi.org/10.1039/c1jm11609f
e-ISSN
13645501
ISSN
09599428
First Page
16877
Last Page
16879
Issue
42
Volume
21
Recommended Citation
Fabijanic, Kristina I.; Perez-Castillejos, Raquel; and Matsui, Hiroshi, "Direct enzyme patterning with microcontact printing and the growth of ZnO nanoparticles on the catalytic templates at room temperature" (2011). Faculty Publications. 11134.
https://digitalcommons.njit.edu/fac_pubs/11134
