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Activation of Nanoparticles by Biosorption for E. coli Detection in Milk and Apple Juice
Author(s) -
Ghinwa Naja,
Pierre Bouvrette,
Julie Champagne,
Roland Brousseau,
John H. T. Luong
Publication year - 2009
Publication title -
applied biochemistry and biotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.558
H-Index - 111
eISSN - 1559-0291
pISSN - 0273-2289
DOI - 10.1007/s12010-009-8709-6
Subject(s) - detection limit , chemistry , polyclonal antibodies , escherichia coli , biosorption , silver nanoparticle , nanoparticle , chromatography , bacteria , biomolecule , sorption , adsorption , microbiology and biotechnology , food science , nanotechnology , biochemistry , materials science , biology , antibody , genetics , organic chemistry , gene , immunology
Two types of silver nanoparticles were activated by specific sorption of biomolecules for the detection of Escherichia coli. The capture of this bacterium was performed using polyclonal antibodies (anti-E. coli) biosorbed onto nanospheres or nanorice through a protein-A layer. The bacterial detection was achieved using surface enhancement Raman scattering in order to compare the performance of these two nanoparticles. The activated silver nanospheres showed a better performance mainly due to the dimension of these nanoparticles. The detection limit has been established using the automated Raman mapping system. The technique was capable of detecting 10(3) cells/mL in milk and apple juice without any pre-enrichment. With an overall assay time less than 1 h, the process could be easily adapted to detect other pathogens by selecting the pertinent antibody. Furthermore, PCR was used for the DNA verification to assess whether the selected bacterial strain was identical before and after detection.

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