Cytochrome P450 monooxygenases of DIBOA biosynthesis: Specificity and conservation among grasses

Erich Glawischnig, Sebastian Grün, Monika Frey, Alfons Gierl

Research output: Contribution to journalArticlepeer-review

59 Scopus citations

Abstract

DIBOA and DIMBOA are secondary metabolites of grasses which function as natural pestizides. The four maize genes BX2 through BX5 encode cytochrome P450-dependent monooxygenases that catalyse four consecutive reactions in the biosynthesis of these secondary products. Although BX2-BX5 share significant sequence homology, the four enzymes have evolved into specific enzymes each catalysing predominantly only one reaction in the pathway. In addition to these natural reactions, BX3 hydroxylates 1,4-benzoxazin-3-one and BX2 shows pCMA demethylase activity. With respect to DIBOA biosynthesis, identical enzymatic reactions have been found in rye as compared to maize, indicating early evolution of the P450 enzymes in the grasses.

Original languageEnglish
Pages (from-to)925-930
Number of pages6
JournalPhytochemistry
Volume50
Issue number6
DOIs
StatePublished - 20 Mar 1999

Keywords

  • Biosynthesis
  • Cyclic hydroxamic acids
  • Cytochrome P450
  • DIBOA
  • DIMBOA
  • Gramineae
  • Yeast expression
  • Zea mays

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