Co-option of the sphingolipid metabolism for the production of nitroalkene defensive chemicals in termite soldiers
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
28126587
DOI
10.1016/j.ibmb.2017.01.008
PII: S0965-1748(17)30008-5
Knihovny.cz E-resources
- Keywords
- Biosynthesis, Chemical defense, Labeled probes, Metabolomics, Prorhinotermes simplex, Transcriptomics,
- MeSH
- Alcohol Oxidoreductases metabolism MeSH
- Amino Acids metabolism MeSH
- Insect Proteins metabolism MeSH
- Isoptera metabolism MeSH
- Ketones metabolism MeSH
- Fatty Acids metabolism MeSH
- Metabolome MeSH
- Nitroparaffins metabolism MeSH
- Serine C-Palmitoyltransferase metabolism MeSH
- Sphingolipids metabolism MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Alcohol Oxidoreductases MeSH
- Amino Acids MeSH
- Insect Proteins MeSH
- Ketones MeSH
- Fatty Acids MeSH
- Nitroparaffins MeSH
- Serine C-Palmitoyltransferase MeSH
- Sphingolipids 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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