Enzymatic formation of a prenyl β-carboline by a fungal indole prenyltransferase

J Nat Med. 2022 Sep;76(4):873-879. doi: 10.1007/s11418-022-01635-0. Epub 2022 Jun 29.

Abstract

CdpNPT from Aspergillus fumigatus is a fungal indole prenyltransferase (IPT) with remarkable substrate promiscuity to generate prenylated compounds. Our first investigation of the catalytic potential of CdpNPT against a β-carboline, harmol (1), revealed that the enzyme also accepts 1 as the prenyl acceptor with dimethylallyl diphosphate (DMAPP) as the prenyl donor and selectively prenylates the C-6 position of 1 by the "regular-type" dimethylallylation to produce 6-(3-dimethylallyl)harmol (2). Furthermore, our X-ray crystal structure analysis of the C-His6-tagged CdpNPT (38-440) truncated mutant complexed with 1 and docking studies of DMAPP to the crystal structure of the CdpNPT (38-440) mutant suggested that CdpNPT could employ the two-step prenylation system to produce 2.

Keywords: Harmol; Indole prenyltransferase; Prenylation; β-Carboline.

MeSH terms

  • Carbolines
  • Dimethylallyltranstransferase* / genetics
  • Dimethylallyltranstransferase* / metabolism
  • Indoles
  • Neoprene
  • Prenylation
  • Substrate Specificity

Substances

  • Carbolines
  • Indoles
  • prenyl
  • Neoprene
  • Dimethylallyltranstransferase