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  Co-option of the sphingolipid metabolism for the production of nitroalkene defensive chemicals in termite soldiers

Jirošová, A., Jančařík, A., Menezes, R. C., Bazalová, O., Dolejšová, K., Vogel, H., et al. (2017). Co-option of the sphingolipid metabolism for the production of nitroalkene defensive chemicals in termite soldiers. Insect Biochemistry and Molecular Biology, 82, 52-61. doi:10.1016/j.ibmb.2017.01.008.

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Jirošová, Anna, Autor
Jančařík, Andrej, Autor
Menezes, Riya Christina1, Autor           
Bazalová, Olga, Autor
Dolejšová, Klára, Autor
Vogel, Heiko2, Autor           
Jedlička, Pavel, Autor
Buček, Aleš, Autor
Brabcová, Jana, Autor
Majer, Pavel, Autor
Hanus, Robert, Autor
Svatoš, Aleš1, Autor           
Affiliations:
1Research Group Mass Spectrometry, MPI for Chemical Ecology, Max Planck Society, ou_421899              
2Department of Entomology, Prof. D. G. Heckel, MPI for Chemical Ecology, Max Planck Society, ou_421895              

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 Zusammenfassung: 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.

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 Datum: 2017-01-202017-01-232017-03
 Publikationsstatus: Erschienen
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 Identifikatoren: Anderer: MS185
DOI: 10.1016/j.ibmb.2017.01.008
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Titel: Insect Biochemistry and Molecular Biology
  Andere : Insect Biochem. Mol. Biol.
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Oxford [England] : Pergamon
Seiten: - Band / Heft: 82 Artikelnummer: - Start- / Endseite: 52 - 61 Identifikator: ISSN: 0965-1748
CoNE: https://pure.mpg.de/cone/journals/resource/954925581163