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Structure elucidation and chemical synthesis of stigmolone, a novel type of prokaryotic pheromone

机译:Stigmolone,一种新型的原核信息素的结构解析和化学合成

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摘要

Approximately 2 μmol of a novel prokaryotic pheromone, involved in starvation-induced aggregation and formation of fruiting bodies by the myxobacterium Stigmatella aurantiaca, were isolated by a large-scale elution procedure. The pheromone was purified by HPLC, and high-resolution MS, IR, 1H-NMR, and 13C-NMR were used to identify the active substance as the hydroxy ketone 2,5,8-trimethyl-8-hydroxy-nonan-4-one, which has been named stigmolone. The analysis was complicated by a solvent-dependent equilibrium between stigmolone and the cyclic enol-ether 3,4-dihydro-2,2,5-trimethyl-6-(2-methylpropyl)-2H-pyran formed by intramolecular nucleophilic attack of the 8-OH group at the ketone C4 followed by loss of H2O. Both compounds were synthesized chemically, and their structures were confirmed by NMR analysis. Natural and synthetic stigmolone have the same biological activity at ca. 1 nM concentration.
机译:通过大规模洗脱程序分离了大约2μmol的新型原核信息素,其参与了由粘胶条形葡萄球菌引起的饥饿诱导的聚集和子实体的形成。通过HPLC纯化信息素,并使用高分辨率MS,IR,1H-NMR和13C-NMR鉴定出活性物质为羟基酮2,5,8-三甲基-8-羟基壬酸-4-一种,已被命名为stigmolone。 stigmolone和环烯醇醚3,4-二氢-2,2,5-三甲基-6-(2-甲基丙基)-2H-吡喃之间的溶剂依赖性平衡使该分析复杂化,分子间亲核攻击酮C4处的8-OH基团随后失去H2O。两种化合物都是化学合成的,其结构通过NMR分析确认。天然和合成的斯蒂格莫隆在大约200℃下具有相同的生物学活性。 1 nM浓度。

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