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Identification of (8S9S10S)-810-dimethyl-1-octalin a key intermediate in the biosynthesis of geosmin in bacteria

机译:鉴定(8S9S10S)-810-二甲基-1-辛醇细菌中土臭素生物合成的关键中间体

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摘要

(−)-Geosmin (>1, blue) is an important odor component produced by many bacteria, including actinomycetes, myxobacteria, and cyanobacteria, but has also been reported for eukaryotic organisms such as fungi, liverworts, insects, and plants. Recent research has shown that the biosynthesis of >1 starts with the cyclization of farnesyl pyrophosphate to (1(10)E,5E)-germacradien-11-ol (>2, yellow), the first key intermediate en route. In a retro-Prins-reaction acetone is lost, and the second key intermediate, (8S,9S,10S)-8,10-dimethyl-1-octalin (>3, red), is formed. After reprotonation, a 1,2-H-shift and attack of water, geosmin is finally released. Octalin >3 occurs in the bouquets of volatiles released by myxobacteria as well as in enzyme extracts of incubation experiments of the purified geosmin synthase from Streptomyces coelicolor. Here the identification of >3, a new natural compound, the elucidation of its stereochemistry, and its synthesis are reported.
机译:(−)-Geosmin(> 1 ,蓝色)是许多细菌(包括放线菌,粘菌和蓝细菌)产生的重要气味成分,但也已报道了真核生物,如真菌,地艾,昆虫和植物。最近的研究表明> 1 的生物合成始于将法呢基焦磷酸环化为(1(10)E,5E)-germacradien-11-ol(> 2 ,黄色),途中的第一个关键点。在逆Prins反应中,丙酮丢失,形成第二个关键中间体((8S,9S,10S)-8,10-二甲基-1-辛醇(> 3 ,红色)”。经过质子化,1,2-H移位和水侵蚀,土臭素最终被释放。 Octalin > 3 发生在粘菌释放的挥发物束中,以及在天蓝色链霉菌纯化的土臭素合酶的孵育实验的酶提取物中。这里报道了> 3 的鉴定,一种新的天然化合物,其立体化学的阐明及其合成。

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