Co-option of the sphingolipid metabolism for the production of nitroalkene defensive chemicals in termite soldiers
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
28126587
DOI
10.1016/j.ibmb.2017.01.008
PII: S0965-1748(17)30008-5
Knihovny.cz E-zdroje
- Klíčová slova
- Biosynthesis, Chemical defense, Labeled probes, Metabolomics, Prorhinotermes simplex, Transcriptomics,
- MeSH
- alkoholoxidoreduktasy metabolismus MeSH
- aminokyseliny metabolismus MeSH
- hmyzí proteiny metabolismus MeSH
- Isoptera metabolismus MeSH
- ketony metabolismus MeSH
- mastné kyseliny metabolismus MeSH
- metabolom MeSH
- nitroparafiny metabolismus MeSH
- serin-C-palmitoyltransferasa metabolismus MeSH
- sfingolipidy metabolismus MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- alkoholoxidoreduktasy MeSH
- aminokyseliny MeSH
- hmyzí proteiny MeSH
- ketony MeSH
- mastné kyseliny MeSH
- nitroparafiny MeSH
- serin-C-palmitoyltransferasa MeSH
- sfingolipidy MeSH
The aliphatic nitroalkene (E)-1-nitropentadec-1-ene (NPD), reported in early seventies in soldiers of the termite genus Prorhinotermes, was the first documented nitro compound produced by insects. Yet, its biosynthetic origin has long remained unknown. Here, we investigated in detail the biosynthesis of NPD in P. simplex soldiers. First, we track the dynamics in major metabolic pathways during soldier ontogeny, with emphasis on likely NPD precursors and intermediates. Second, we propose a hypothesis of NPD formation and verify its individual steps using in vivo incubations of putative precursors and intermediates. Third, we use a de novo assembled RNA-Seq profiles of workers and soldiers to identify putative enzymes underlying NPD formation. And fourth, we describe the caste- and age-specific expression dynamics of candidate initial genes of the proposed biosynthetic pathway. Our observations provide a strong support to the following biosynthetic scenario of NPD formation, representing an analogy of the sphingolipid pathway starting with the condensation of tetradecanoic acid with l-serine and leading to the formation of a C16 sphinganine. The C16 sphinganine is then oxidized at the terminal carbon to give rise to 2-amino-3-hydroxyhexadecanoic acid, further oxidized to 2-amino-3-oxohexadecanoic acid. Subsequent decarboxylation yields 1-aminopentadecan-2-one, which then proceeds through six-electron oxidation of the amino moiety to give rise to 1-nitropentadecan-2-one. Keto group reduction and hydroxyl moiety elimination lead to NPD. The proposed biosynthetic sequence has been constructed from age-related quantitative dynamics of individual intermediates and confirmed by the detection of labeled products downstream of the administered labeled intermediates. Comparative RNA-Seq analyses followed by qRT-PCR validation identified orthologs of serine palmitoyltransferase and 3-ketodihydrosphingosine reductase genes as highly expressed in the NPD production site, i.e. the frontal gland of soldiers. A dramatic onset of expression of the two genes in the first days of soldier's life coincides with the start of NPD biosynthesis, giving further support to the proposed biosynthetic hypothesis.
Biology Centre CAS Branišovská 31 CZ 37005 České Budějovice Czechia
Max Planck Institute for Chemical Ecology Hans Knöll Str 8 07745 Jena Germany
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