4.5 Review

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

Journal

JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY
Volume 44, Issue 4-5, Pages 517-524

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s10295-016-1850-7

Keywords

beta-lactams; Penicillin; Cephalosporin; ACVS; Streptomyces; Protein purification

Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. NSERC
  3. MUN

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The delta-(L-alpha-aminoadipyl)-L-cysteinyl-D-valine (ACV) tripeptide is the first dedicated intermediate in the biosynthetic pathway leading to the penicillin and cephalosporin classes of beta-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.

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