聚酮
链霉菌
立体化学
二维核磁共振波谱
核磁共振波谱
四氢萘酮
化学
拉伤
发色团
生物
细菌
有机化学
生物化学
基因
生物合成
遗传学
解剖
作者
Víctor Rodríguez Martín-Aragón,Francisco Millán,Cristina Cuadrado,Antonio Hernández Daranas,Antonio Fernández Medarde,José M. Sánchez López
出处
期刊:Marine Drugs
[MDPI AG]
日期:2023-10-03
卷期号:21 (10): 526-526
被引量:2
摘要
Using the OSMAC (One Strain Many Compounds) approach, the actinobacterium Streptomyces griseorubiginosus, derived from an unidentified cnidarian collected from a reef near Pointe de Bellevue in Réunion Island (France), was subjected to cultivation under diverse conditions. This endeavour yielded the isolation of a repertoire of 23 secondary metabolites (1-23), wherein five compounds were unprecedented as natural products (19-23). Specifically, compounds 19 and 20 showcased novel anthrone backbones, while compound 23 displayed a distinctive tetralone structure. Additionally, compounds 21 and 22 presented an unusual naphtho [2,3-c]furan-4(9H)-one chromophore. Interestingly, the detection of all these novel compounds (19-23) was exclusively achieved when the bacterium was cultured in FA-1 liquid medium supplemented with the epigenetic modifier γ-butyrolactone. The elucidation of the structural features of the newfound compounds was accomplished through a combination of HRESIMS, 1D and 2D NMR spectroscopy, as well as QM-NMR (Quantum Mechanical-Nuclear Magnetic Resonance) methods and by comparison with existing literature. Moreover, the determination of the relative configuration of compound 23 was facilitated by employing the mix-J-DP4 computational approach.
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