Wittmann Isabel, Schierling Andreas, Dettner Konrad, Göhl Matthias, Schmidt Jürgen, Seifert Karlheinz
Lehrstuhl für Organische Chemie, NW II, Universität Bayreuth, DE-95440 Bayreuth, (phone: +49-921-553098; fax: +49-921-555358).
Lehrstuhl für Tierökologie II, Universität Bayreuth, DE-95440 Bayreuth.
Chem Biodivers. 2015 Sep;12(9):1422-34. doi: 10.1002/cbdv.201400391.
Rove beetles of the genus Stenus produce and store bioactive alkaloids like stenusine (3), 3-(2-methylbut-1-enyl)pyridine (4), and cicindeloine (5) in their pygidial glands to protect themselves from predation and microorganismic infestation. The biosynthesis of stenusine (3), 3-(2-methylbut-1-enyl)pyridine (4), and cicindeloine (5) was previously investigated in Stenus bimaculatus, Stenus similis, and Stenus solutus, respectively. The piperideine alkaloid cicindeloine (5) occurs also as a major compound in the pygidial gland secretion of Stenus cicindeloides. The three metabolites follow the same biosynthetic pathway, where the N-heterocyclic ring is derived from L-lysine and the side chain from L-isoleucine. The different alkaloids are finally obtained by few modifications of shared precursor molecules, such as 2,3,4,5-tetrahydro-5-(2-methylbutylidene)pyridine (1). This piperideine alkaloid was synthesized and detected by GC/MS and GC at a chiral phase in the pygidial glands of Stenus similis, Stenus tarsalis, and Stenus cicindeloides.
Stenus属的隐翅虫在其臀腺中产生并储存生物活性生物碱,如stenusine(3)、3-(2-甲基丁-1-烯基)吡啶(4)和cicindeloine(5),以保护自己免受捕食和微生物侵扰。此前分别在双斑 Stenus bimaculatus、相似 Stenus similis和 Solutus Stenus solutus中研究了stenusine(3)、3-(2-甲基丁-1-烯基)吡啶(4)和cicindeloine(5)的生物合成。哌啶生物碱cicindeloine(5)也是 Cicindeloides Stenus臀腺分泌物中的主要化合物。这三种代谢物遵循相同的生物合成途径,其中N-杂环源自L-赖氨酸,侧链源自L-异亮氨酸。通过对共享前体分子(如2,3,4,5-四氢-5-(2-甲基亚丁基)吡啶(1))进行少量修饰,最终获得了不同的生物碱。这种哌啶生物碱已在相似 Stenus similis、跗节 Stenus tarsalis和 Cicindeloides Stenus的臀腺中通过气相色谱-质谱联用(GC/MS)和手性相气相色谱(GC)进行了合成和检测。