Sphinganine-like biogenesis of (E)-1-nitropentadec-1-ene in termite soldiers of the genus Prorhinotermes

Chembiochem. 2014 Mar 3;15(4):533-6. doi: 10.1002/cbic.201300665. Epub 2014 Jan 23.

Abstract

In 1974, (E)-1-nitropentadec-1-ene, a strong lipophilic contact poison of soldiers of the termite genus Prorhinotermes, was the first-described insect-produced nitro compound. However, its biosynthesis remained unknown. In the present study, we tested the hypothesis that (E)-1-nitropentadec-1-ene biosynthesis originates with condensation of amino acids with tetradecanoic acid. By using in vivo experiments with radiolabeled and deuterium-labeled putative precursors, we show that (E)-1-nitropentadec-1-ene is synthesized by the soldiers from glycine or L-serine and tetradecanoic acid. We propose and discuss three possible biosynthetic pathways.

Keywords: Prorhinotermes; biosynthesis; natural products; nitro compounds; termites.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / chemistry
  • Amino Acids / metabolism
  • Animals
  • Deuterium / chemistry
  • Isoptera / chemistry*
  • Isoptera / metabolism
  • Isotope Labeling
  • Myristic Acid / chemistry
  • Myristic Acid / metabolism
  • Naphthalenes / chemistry
  • Naphthalenes / metabolism*
  • Sphingosine / analogs & derivatives*
  • Sphingosine / chemistry
  • Stereoisomerism

Substances

  • Amino Acids
  • Naphthalenes
  • Myristic Acid
  • 1-nitronaphthalene
  • Deuterium
  • Sphingosine
  • safingol