Penicillin-binding proteins in Actinobacteria

J Antibiot (Tokyo). 2015 Apr;68(4):223-45. doi: 10.1038/ja.2014.148. Epub 2014 Oct 29.

Abstract

Because some Actinobacteria, especially Streptomyces species, are β-lactam-producing bacteria, they have to have some self-resistant mechanism. The β-lactam biosynthetic gene clusters include genes for β-lactamases and penicillin-binding proteins (PBPs), suggesting that these are involved in self-resistance. However, direct evidence for the involvement of β-lactamases does not exist at the present time. Instead, phylogenetic analysis revealed that PBPs in Streptomyces are distinct in that Streptomyces species have much more PBPs than other Actinobacteria, and that two to three pairs of similar PBPs are present in most Streptomyces species examined. Some of these PBPs bind benzylpenicillin with very low affinity and are highly similar in their amino-acid sequences. Furthermore, other low-affinity PBPs such as SCLAV_4179 in Streptomyces clavuligerus, a β-lactam-producing Actinobacterium, may strengthen further the self-resistance against β-lactams. This review discusses the role of PBPs in resistance to benzylpenicillin in Streptomyces belonging to Actinobacteria.

Publication types

  • Review

MeSH terms

  • Actinobacteria / drug effects
  • Actinobacteria / genetics
  • Actinobacteria / metabolism*
  • Amino Acid Sequence
  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Drug Resistance, Bacterial
  • Humans
  • Multigene Family / genetics
  • Penicillin G / pharmacology
  • Penicillin-Binding Proteins / metabolism*
  • Phylogeny
  • Streptomyces / drug effects
  • Streptomyces / genetics
  • Streptomyces / metabolism*
  • beta-Lactamases / genetics
  • beta-Lactams / metabolism

Substances

  • Anti-Bacterial Agents
  • Penicillin-Binding Proteins
  • beta-Lactams
  • beta-Lactamases
  • Penicillin G