Correlation Engine 2.0
Clear Search sequence regions


  • antisera (1)
  • bacteria proteins (1)
  • bind (1)
  • cell (4)
  • cell wall (1)
  • dehydrogenases (1)
  • enzymes (6)
  • factors (2)
  • fibrinogen (1)
  • GapA (4)
  • host (3)
  • human (6)
  • human cells (1)
  • Ldh (3)
  • lung (1)
  • mycoplasma (4)
  • pathogen (1)
  • PdhB (2)
  • plasmin (2)
  • Plasminogen (9)
  • pneumonia mycoplasma (1)
  • proteolysis (1)
  • Pyk (2)
  • Sizes of these terms reflect their relevance to your search.

    In different bacteria, primarily cytosolic and metabolic proteins are characterized as surface localized and interacting with different host factors. These moonlighting proteins include glycolytic enzymes, and it has been hypothesized that they influence the virulence of pathogenic species. The presence of surface-displayed glycolytic enzymes and their interaction with human plasminogen as an important host factor were investigated in the genome-reduced and cell wall-less microorganism Mycoplasma pneumoniae, a common agent of respiratory tract infections of humans. After successful expression of 19 glycolytic enzymes and production of polyclonal antisera, the localization of proteins in the mycoplasma cell was characterized using fractionation of total proteins, colony blot, mild proteolysis and immunofluorescence of M. pneumoniae cells. Eight glycolytic enzymes, pyruvate dehydrogenases A to C (PdhA-C), glyceraldehyde-3-phosphate dehydrogenase (GapA), lactate dehydrogenase (Ldh), phosphoglycerate mutase (Pgm), pyruvate kinase (Pyk), and transketolase (Tkt), were confirmed as surface expressed and all are able to interact with plasminogen. Plasminogen bound to recombinant proteins PdhB, GapA, and Pyk was converted to plasmin in the presence of urokinase plasminogen activator and plasmin-specific substrate d-valyl-leucyl-lysine-p-nitroanilide dihydrochloride. Furthermore, human fibrinogen was degraded by the complex of plasminogen and recombinant protein PdhB or Pgm. In addition, surface-displayed proteins (except PdhC) bind to human lung epithelial cells, and the interaction was reduced significantly by preincubation of cells with antiplasminogen. Our results suggest that plasminogen binding and activation by different surface-localized glycolytic enzymes of M. pneumoniae may play a role in successful and long-term colonization of the human respiratory tract. Copyright © 2016, American Society for Microbiology. All Rights Reserved.

    Citation

    Anne Gründel, Melanie Pfeiffer, Enno Jacobs, Roger Dumke. Network of Surface-Displayed Glycolytic Enzymes in Mycoplasma pneumoniae and Their Interactions with Human Plasminogen. Infection and immunity. 2016 Mar;84(3):666-76

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 26667841

    View Full Text