-
Something wrong with this record ?
Co-option of the sphingolipid metabolism for the production of nitroalkene defensive chemicals in termite soldiers
A. Jirošová, A. Jančařík, RC. Menezes, O. Bazalová, K. Dolejšová, H. Vogel, P. Jedlička, A. Buček, J. Brabcová, P. Majer, R. Hanus, A. Svatoš,
Language English Country England, Great Britain
Document type Journal Article
- 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
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
Faculty of Science Charles University Prague Viničná 7 128 44 Prague Czechia
Max Planck Institute for Chemical Ecology Hans Knöll Str 8 07745 Jena Germany
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc17031090
- 003
- CZ-PrNML
- 005
- 20171031103021.0
- 007
- ta
- 008
- 171025s2017 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.ibmb.2017.01.008 $2 doi
- 035 __
- $a (PubMed)28126587
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Jirošová, Anna $u The Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo n. 2, 166 10 Prague, Czechia.
- 245 10
- $a Co-option of the sphingolipid metabolism for the production of nitroalkene defensive chemicals in termite soldiers / $c A. Jirošová, A. Jančařík, RC. Menezes, O. Bazalová, K. Dolejšová, H. Vogel, P. Jedlička, A. Buček, J. Brabcová, P. Majer, R. Hanus, A. Svatoš,
- 520 9_
- $a 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.
- 650 _2
- $a alkoholoxidoreduktasy $x metabolismus $7 D000429
- 650 _2
- $a aminokyseliny $x metabolismus $7 D000596
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a mastné kyseliny $x metabolismus $7 D005227
- 650 _2
- $a hmyzí proteiny $x metabolismus $7 D019476
- 650 _2
- $a Isoptera $x metabolismus $7 D020049
- 650 _2
- $a ketony $x metabolismus $7 D007659
- 650 _2
- $a metabolom $7 D055442
- 650 _2
- $a nitroparafiny $x metabolismus $7 D009595
- 650 _2
- $a serin-C-palmitoyltransferasa $x metabolismus $7 D051102
- 650 _2
- $a sfingolipidy $x metabolismus $7 D013107
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Jančařík, Andrej $u The Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo n. 2, 166 10 Prague, Czechia.
- 700 1_
- $a Menezes, Riya C $u Max-Planck Institute for Chemical Ecology, Hans-Knöll-Str. 8, 07745 Jena, Germany.
- 700 1_
- $a Bazalová, Olga $u Biology Centre CAS, Branišovská 31, CZ-37005 České Budějovice, Czechia.
- 700 1_
- $a Dolejšová, Klára $u The Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo n. 2, 166 10 Prague, Czechia; Faculty of Science, Charles University in Prague, Viničná 7, 128 44 Prague, Czechia.
- 700 1_
- $a Vogel, Heiko $u Max-Planck Institute for Chemical Ecology, Hans-Knöll-Str. 8, 07745 Jena, Germany.
- 700 1_
- $a Jedlička, Pavel $u The Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo n. 2, 166 10 Prague, Czechia.
- 700 1_
- $a Buček, Aleš $u The Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo n. 2, 166 10 Prague, Czechia.
- 700 1_
- $a Brabcová, Jana $u The Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo n. 2, 166 10 Prague, Czechia.
- 700 1_
- $a Majer, Pavel $u The Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo n. 2, 166 10 Prague, Czechia.
- 700 1_
- $a Hanus, Robert $u The Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo n. 2, 166 10 Prague, Czechia. Electronic address: robert@uochb.cas.cz.
- 700 1_
- $a Svatoš, Aleš $u The Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo n. 2, 166 10 Prague, Czechia; Max-Planck Institute for Chemical Ecology, Hans-Knöll-Str. 8, 07745 Jena, Germany. Electronic address: svatos@ice.mpg.de.
- 773 0_
- $w MED00004948 $t Insect biochemistry and molecular biology $x 1879-0240 $g Roč. 82, č. - (2017), s. 52-61
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/28126587 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20171025 $b ABA008
- 991 __
- $a 20171031103112 $b ABA008
- 999 __
- $a ok $b bmc $g 1254683 $s 992117
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2017 $b 82 $c - $d 52-61 $e 20170123 $i 1879-0240 $m Insect biochemistry and molecular biology $n Insect Biochem Mol Biol $x MED00004948
- LZP __
- $a Pubmed-20171025