Two-dimensional fluorescence difference gel electrophoretic analysis of Streptococcus mutans biofilms

J Proteome Res. 2005 Nov-Dec;4(6):2161-73. doi: 10.1021/pr0502471.

Abstract

Compared with traditional two-dimensional (2D) proteome analysis of Streptococcus mutans grown as a biofilm from a planktonic culture at steady state (Rathsam et al., Microbiol. 2005, 151, 1823-1837), the use of 2D fluorescence difference gel electrophoresis (DIGE) led to a 3-fold increase in the number of identified protein spots that were significantly altered in their level of expression (P < 0.050). Of the 73 identified proteins, only nine were up-regulated in biofilm grown cells. The results supported the previously surmised hypothesis that general metabolic functions were down-regulated in response to a reduction in growth rate in mature S. mutans biofilms. Up-regulation of competence proteins without any concomitant increase in stress-responsive proteins was confirmed, while the levels of glucosyltransferase C (GtfC), involved in glucan formation, O-acetylserine sulfhyrylase (cysteine synthetase A; CsyK), implicated in the formation of [Fe-S] clusters, and a hypothetical protein encoded by the open reading frame, SMu0188, were also up-regulated.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Bacterial Proteins / chemistry*
  • Base Sequence
  • Biofilms*
  • Cell Proliferation
  • Cysteine Synthase / metabolism
  • Down-Regulation
  • Electrophoresis, Gel, Two-Dimensional / methods*
  • Glucans / chemistry
  • Glucans / metabolism
  • Glucosyltransferases / metabolism
  • Hydrogen-Ion Concentration
  • Iron-Sulfur Proteins / chemistry
  • Molecular Sequence Data
  • Mutation
  • Open Reading Frames
  • Phosphoenolpyruvate / chemistry
  • Phosphotransferases / metabolism
  • Plankton / metabolism
  • Proteins / chemistry
  • Proteome
  • Proteomics / methods*
  • Streptococcus mutans / metabolism*
  • Up-Regulation

Substances

  • Bacterial Proteins
  • Glucans
  • Iron-Sulfur Proteins
  • Proteins
  • Proteome
  • Phosphoenolpyruvate
  • Glucosyltransferases
  • glucosyltransferase C
  • Cysteine Synthase
  • Phosphotransferases