Quantitative protein expression and cell surface characteristics of Escherichia coli MG1655 biofilms

Proteomics. 2011 Feb;11(3):339-51. doi: 10.1002/pmic.201000386. Epub 2011 Jan 3.

Abstract

Cell surface physicochemical characterization techniques were combined with quantitative changes in protein expression, to investigate the biological and biophysical changes of Escherichia coli MG1655 cells when grown as a biofilm (BIO). The overall surface charge of BIO cells was found to be less negative, highlighting the need for a lower electrophoretic mobility for attachment to occur. Comparison of the chemical functional groups on the cell surface showed similar profiles, with the absorbance intensity higher for proteins and carbohydrates in the BIO cells. Quantitative proteomic analysis demonstrated that 3 proteins were significantly increased, and 9 proteins significantly decreased in abundance, in cells grown as a BIO compared to their planktonic counterparts, with 7 of these total 12 proteins unique to this study. Proteins showing significant increased or decreased abundance include proteins involved in acid resistance, DNA protection and binding and ABC transporters. Further predictive analysis of the metabolic pathways showed an increased abundance of the amino acid metabolism and tricarboxylic acid (TCA) cycle, with a decrease in expression within the pentose phosphate and glycolysis pathways. It is therefore hypothesized that cells grown as a BIO are still energetically viable potentially using amino acids as an indirect carbon backbone source into the TCA cycle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biofilms*
  • Citric Acid Cycle*
  • Electrophoresis, Gel, Two-Dimensional
  • Escherichia coli / physiology*
  • Escherichia coli Proteins / metabolism*
  • Membrane Proteins / metabolism*
  • Peptide Mapping
  • Proteome / analysis*
  • Proteomics
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

Substances

  • Escherichia coli Proteins
  • Membrane Proteins
  • Proteome