Enzyme Stabilization in Various Nanostructured Materials
Byoung Chan Kim, Gwangju Institute of Science and Technology, Gwangju, South Korea, Jungbae Kim, Pacific Northwest National Laboratory, 902 Battelle Blvd., PO Box 999, Mailstop K8-93, Richland, WA 99352, Seong H. Kim, Penn State University, 118-B Fenske Lab, University Park, PA 16802-4400, Taeghwan Hyeon, National Creative Research Center for Oxide Nanocrystalline Materials and School of Chemical and Biological Engineering, Seoul National University, Seoul, South Korea and Man Bock Gu, Graduate School of Biotechnology, Korea University, Seoul, South Korea

Efforts using nanostructured materials are an intriguing approach for developing composite of enzyme-nanomaterials since these materials can provide a large surface area, which can lead high volumetric enzyme activity. Recent advances in enzyme aggregation via cross-linking are promising for the development of highly stable catalytic composite of bio-nanomaterials. Significant enhancement of enzyme stabilization was realized as introducing cross-linked enzyme aggregates (CLEAs) via glutaraldehyde mediated coupling with various nanostructured materials such as nanofiber, carbon nanotube, or mesoporous silica. The enzyme stability of enzyme aggregated nanomaterials was greatly enhanced with essentially no measurable loss of activity over a month or several days of observation under rigorous shaking condition. This approach of enzyme aggregation with various nanostructure materials, yielding high activity and stability, creates a useful new biocatalytic immobilized enzyme system with potential applications in biosensor, bioelectrochemistry, bioremediation and bioconversion.

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Nanotechnology in Biocatalysis II

The Preliminary Program for 2005 Annual Meeting (Cincinnati, OH)