δ-(L-α-aminoadipyl)-L-cysteinyl-D-valine synthetase (ACVS): discovery and perspectives

J Ind Microbiol Biotechnol. 2017 May;44(4-5):517-524. doi: 10.1007/s10295-016-1850-7. Epub 2016 Oct 20.

Abstract

The δ-(L-α-aminoadipyl)-L-cysteinyl-D-valine (ACV) tripeptide is the first dedicated intermediate in the biosynthetic pathway leading to the penicillin and cephalosporin classes of β-lactam natural products in bacteria and fungi. It is synthesized nonribosomally by the ACV synthetase (ACVS) enzyme, which has been purified and partially characterized from many sources. Due to its large size and instability, many details regarding the reaction mechanism of ACVS are still not fully understood. In this review we discuss the chronology and associated methodology that led to the discovery of ACVS, some of the main findings regarding its activities, and some recent/current studies being conducted on the enzyme. In addition, we conclude with perspectives on what can be done to increase our understating of this very important protein in the future.

Keywords: ACVS; Cephalosporin; Penicillin; Protein purification; Streptomyces; β-lactams.

Publication types

  • Review

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Genes, Bacterial*
  • Genes, Fungal*
  • Oligopeptides / chemistry
  • Penicillium chrysogenum / enzymology
  • Penicillium chrysogenum / genetics
  • Peptide Synthases / genetics*
  • Peptide Synthases / metabolism*
  • Streptomyces / enzymology
  • Streptomyces / genetics

Substances

  • Bacterial Proteins
  • Oligopeptides
  • 5-(2-aminoadipyl)cysteinylvaline
  • Peptide Synthases
  • alpha-aminoadipyl-cysteinyl-valine synthetase