Molecular and biochemical characterization of Catharanthus roseus perivine-Nβ-methyltransferase

Phytochemistry. 2022 Sep:201:113266. doi: 10.1016/j.phytochem.2022.113266. Epub 2022 Jun 6.

Abstract

The biosynthesis of monoterpenoid indole alkaloids in Catharanthus roseus has been most extensively studied, leading to the detailed characterization of the pathway for the formation of their well-known anticancer alkaloids. The present study describes the identification, molecular cloning, and functional expression of C. roseus perivine-Nβ-methyltransferase (PeNMT) that converts perivine to Nβ-methylperivine (vobasine). PeNMT is member of a recently discovered γ-tocopherol-like N-methyltransferase (γ-TLMT) gene family that displays high substrate specificity and that appears to have evolved in the Vinceae tribe of Apocynaceae family where most N-methylated MIAs have been identified in the phytochemical literature.

Keywords: Apocynaceae; Assembly of periformyline; Catharanthus roseus; Madagascar periwinkle; Monoterpenoid indole alkaloid biosynthesis; Perivine-N(β)-methyltransferase; Tocopherol like methyltransferase.

MeSH terms

  • Apocynaceae*
  • Catharanthus* / metabolism
  • Gene Expression Regulation, Plant
  • Indole Alkaloids / chemistry
  • Methyltransferases / genetics
  • Methyltransferases / metabolism
  • Phytochemicals / metabolism
  • Plant Proteins / metabolism
  • Secologanin Tryptamine Alkaloids* / metabolism

Substances

  • Indole Alkaloids
  • Phytochemicals
  • Plant Proteins
  • Secologanin Tryptamine Alkaloids
  • Methyltransferases