4.5 Article

Identification of the incednine biosynthetic gene cluster: characterization of novel β-glutamate-β-decarboxylase IdnL3

Journal

JOURNAL OF ANTIBIOTICS
Volume 66, Issue 12, Pages 691-699

Publisher

JAPAN ANTIBIOTICS RESEARCH ASSOC
DOI: 10.1038/ja.2013.76

Keywords

biosynthesis; enzyme; gene cluster; beta-glutamate-beta-decarboxylase; macrolactam; polyketide; Streptomyces

Funding

  1. the Ministry of Education, Culture, Sports, Science and Technology
  2. Nagase Science and Technology Foundation
  3. Takeda Science Foundation
  4. Grants-in-Aid for Scientific Research [22108003] Funding Source: KAKEN

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A biosynthetic gene cluster for the 24-membered macrolactam antibiotic incednine was identified from the producer strain, Streptomyces sp. ML694-90F3. Among the putative incednine biosynthetic enzymes, a novel pyridoxal 5'-phosphate (PLP)-dependent beta-glutamate-beta-decarboxylase, IdnL3, was functionally characterized in vitro by demonstrating its (S)-3-aminobutyrate- forming activity with beta-glutamate in the presence of PLP. Because (S)-3-aminobutyrate is known for the direct precursor of incednine, this enzyme supplies the unique beta-amino acid starter unit. The identified gene cluster encodes five characteristic b-amino acid carrying enzymes, consisting of a pathway-specific ATP-dependent ligase, a discrete acyl carrier protein (ACP), beta-aminoacyl-ACP b-amino group-protecting ATP-dependent ligase, dipeptidyl-ACP: PKS-loading ACP dipeptidyltransferase and a terminal amino acid peptidase, which are completely conserved in beta-amino acid-containing macrolactam biosynthetic gene clusters. Overall, a plausible biosynthetic pathway for incednine was proposed.

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