Jirošová Anna, Jančařík Andrej, Menezes Riya C, Bazalová Olga, Dolejšová Klára, Vogel Heiko, Jedlička Pavel, Buček Aleš, Brabcová Jana, Majer Pavel, Hanus Robert, Svatoš Aleš
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.
Insect Biochem Mol Biol. 2017 Mar;82:52-61. doi: 10.1016/j.ibmb.2017.01.008. Epub 2017 Jan 23.
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 C sphinganine. The C 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.
脂肪族硝基烯烃(E)-1-硝基十五碳-1-烯(NPD)于20世纪70年代初在原鼻白蚁属的兵蚁中被发现,是昆虫产生的首个有记录的硝基化合物。然而,其生物合成起源长期以来一直未知。在此,我们详细研究了简单原鼻白蚁兵蚁中NPD的生物合成。首先,我们追踪了兵蚁个体发育过程中主要代谢途径的动态变化,重点关注可能的NPD前体和中间体。其次,我们提出了NPD形成的假说,并通过对假定前体和中间体进行体内孵育来验证其各个步骤。第三,我们利用从头组装的工蚁和兵蚁RNA-Seq图谱来鉴定NPD形成背后的假定酶。第四,我们描述了所提出的生物合成途径中候选起始基因在不同品级和年龄阶段的表达动态。我们的观察结果有力地支持了以下NPD形成的生物合成过程,该过程类似于鞘脂途径,始于十四烷酸与L-丝氨酸的缩合,进而形成C-鞘氨醇。然后C-鞘氨醇在末端碳上被氧化,生成2-氨基-3-羟基十六烷酸,进一步氧化为2-氨基-3-氧代十六烷酸。随后的脱羧反应产生1-氨基十五烷-2-酮,然后通过氨基部分的六电子氧化生成1-硝基十五烷-2-酮。酮基还原和羟基消除导致NPD的产生。所提出的生物合成序列是根据各个中间体与年龄相关的定量动态构建的,并通过检测施用标记中间体下游的标记产物得到证实。比较RNA-Seq分析随后进行qRT-PCR验证,确定丝氨酸棕榈酰转移酶和3-酮二氢鞘氨醇还原酶基因的直系同源物在NPD产生部位即兵蚁的额腺中高度表达。这两个基因在兵蚁生命最初几天的显著表达起始与NPD生物合成的开始相吻合,进一步支持了所提出的生物合成假说。