Colorimetric bacteria sensing using a supramolecular enzyme-nanoparticle biosensor

J Am Chem Soc. 2011 Jun 29;133(25):9650-3. doi: 10.1021/ja2021729. Epub 2011 Jun 7.

Abstract

Rapid and sensitive detection of pathogens is a key requirement for both environmental and clinical settings. We report here a colorimetric enzyme-nanoparticle conjugate system for detection of microbial contamination. In this approach, cationic gold nanoparticles (NPs) featuring quaternary amine headgroups are electrostatically bound to an enzyme [β-galactosidase (β-Gal)], inhibiting enzyme activity. Analyte bacteria bind to the NP, which releases the β-Gal and restores its activity, providing an enzyme-amplified colorimetric readout of the binding event. Using this strategy, we have been able to quantify bacteria at concentrations of 1 × 10(2) bacteria/mL in solution and 1 × 10(4) bacteria/mL in a field-friendly test strip format.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Bacteria / isolation & purification*
  • Bacterial Load / instrumentation
  • Bacterial Load / methods*
  • Biosensing Techniques / methods*
  • Colorimetry / methods*
  • Gold
  • Metal Nanoparticles
  • Nanoparticles
  • beta-Galactosidase / metabolism

Substances

  • Gold
  • beta-Galactosidase