4.5 Article

Modification of glucose oxidase for the development of biocatalytic solvent inks

期刊

ENZYME AND MICROBIAL TECHNOLOGY
卷 55, 期 -, 页码 21-25

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.enzmictec.2013.11.001

关键词

Ion pairing; Glucose oxidase; Inkjet printing; Immobilization; Deposition; Nanocomposites

资金

  1. USDA National Institutes of Food and Agriculture
  2. UMass Amherst Center for Hierarchical Manufacturing, a nanoscience shared facility
  3. National Science Foundation [CMMI-1025020]

向作者/读者索取更多资源

Inkjet printing of enzymes onto hydrophobic polymeric material offers the potential for economical rapid deposition and patterning of biocatalysts for biosensor, microarray, and intelligent packaging applications. Non-polar solvent based inks provide simple vehicles for direct printing on these materials; however, enzymes are not readily soluble in such inks. Glucose oxidase (Aspergillus niger) was made soluble in toluene by hydrophobic ion pairing with didodecyldimethylammonium bromide. Following modification, single enzyme composites with a mean diameter of 12.5 nm were formed. The enzymes showed no significant change in K-m' and a 46% decrease in k(cat)' compared to the native enzyme. Modification allowed for direct printing and patterning on PET using piezoelectric inkjet printing. Specific activity of the modified enzyme was reduced from 889 x 10(3) mu mol/min/g to 2 x 10(3) mu mol/min/g after printing. These results suggest that direct inkjet printing of enzymes onto hydrophobic polymers may be accomplished using enzyme modification as a means to induce solubility in solvent inks. (C) 2013 Elsevier Inc. All rights reserved.

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