Sphinganine-like biogenesis of (E)-1-nitropentadec-1-ene in termite soldiers of the genus Prorhinotermes
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24458870
DOI
10.1002/cbic.201300665
Knihovny.cz E-zdroje
- Klíčová slova
- Prorhinotermes, biosynthesis, natural products, nitro compounds, termites,
- MeSH
- aminokyseliny chemie metabolismus MeSH
- deuterium chemie MeSH
- Isoptera chemie metabolismus MeSH
- izotopové značení MeSH
- kyselina myristová chemie metabolismus MeSH
- naftaleny chemie metabolismus MeSH
- sfingosin analogy a deriváty chemie MeSH
- stereoizomerie MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 1-nitronaphthalene MeSH Prohlížeč
- aminokyseliny MeSH
- deuterium MeSH
- kyselina myristová MeSH
- naftaleny MeSH
- safingol MeSH Prohlížeč
- sfingosin MeSH
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.
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