Quantifying the effect of covalently immobilized enzymes on biofilm formation by atomic force microscopy-based single-cell force spectroscopy

Macromol Rapid Commun. 2012 Sep 14;33(17):1453-8. doi: 10.1002/marc.201200359. Epub 2012 Jul 25.

Abstract

A novel atomic force microscopy-based single-cell force spectroscopy assay to quantify the adhesion of bacterial cells to surfaces was developed. The assay was applied to quantify the effect of two biofilm-degrading enzymes, the protease Subtilisin A and glycoside hydrolase cellulase, on the attachment of the biofilm-forming bacterial strain Cobetia marina. Insights on the mechanism of the initial adhesion and on the nature of the adhesion-mediating molecules were gained. The assay can be easily adapted to various other substrates, different bacterial strains and other fouling species (e.g., algae and diatoms).

MeSH terms

  • Biofilms*
  • Biofouling
  • Enzymes, Immobilized / chemistry
  • Enzymes, Immobilized / metabolism
  • Gammaproteobacteria / physiology
  • Glycoside Hydrolases / chemistry
  • Glycoside Hydrolases / metabolism*
  • Microscopy, Atomic Force
  • Subtilisins / chemistry
  • Subtilisins / metabolism*

Substances

  • Enzymes, Immobilized
  • Glycoside Hydrolases
  • Subtilisins