Structure, biochemistry and mechanism of action of glycopeptide antibiotics

Eur J Clin Microbiol Infect Dis. 1989 Nov;8(11):943-50. doi: 10.1007/BF01967563.


Glycopeptide antibiotics, including vancomycin and teicoplanin, are large, rigid molecules that inhibit a late stage in bacterial cell wall peptidoglycan synthesis. The three-dimensional structure contains a cleft into which peptides of highly specific configuration (L-aa-D-aa-D-aa) can fit: such sequences are found only in bacterial cell walls, hence glycopeptides are selectively toxic. Glycopeptides interact with peptides of this conformation by hydrogen bonding, forming stable complexes. As a result of binding to L-aa-D-Ala-D-Ala groups in wall intermediates, glycopeptides inhibit, apparently by steric hindrance, the formation of the backbone glycan chains (catalysed by peptidoglycan polymerase) from the simple wall subunits as they are extruded through the cytoplasmic membrane. The subsequent transpeptidation reaction that imparts rigidity to the cell wall is also thus inhibited. This unique mechanism of action, involving binding of the bulky inhibitor to the substrate outside the membrane so that the active sites of two enzymes cannot align themselves correctly, renders the acquisition of resistance to the glycopeptide antibiotics more difficult than that to the majority of the other antibiotic groups.

Publication types

  • Review

MeSH terms

  • Amino Acid Sequence
  • Anti-Bacterial Agents* / metabolism
  • Anti-Bacterial Agents* / pharmacology
  • Bacteria / drug effects
  • Cell Wall / metabolism
  • Drug Resistance, Microbial
  • Glycopeptides* / metabolism
  • Glycopeptides* / pharmacology
  • Humans
  • Models, Molecular
  • Molecular Sequence Data
  • Molecular Structure
  • Peptidoglycan / biosynthesis
  • Teicoplanin
  • Vancomycin / metabolism
  • Vancomycin / pharmacology


  • Anti-Bacterial Agents
  • Glycopeptides
  • Peptidoglycan
  • Teicoplanin
  • Vancomycin