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Two antibacterial and PPARα/γ-agonistic unsaturated keto fatty acids from a coral-associated actinomycete of the genus Micrococcus

机译:两种抗菌和PPARα/γ-激动的不饱和酮脂肪酸来自珊瑚相关的鳞片菌属的珊瑚胶质细胞

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摘要

A pair of geometrically isomeric unsaturated keto fatty acids, (6E,8Z)- and (6E,8E)-5-oxo-6,8-tetradecadienoic acids (1 and 2), were isolated from the culture broth of an actinomycete of the genus Micrococcus, which was associated with a stony coral, Catalaphyllia sp. Their chemical structures were elucidated by spectroscopic analysis including NMR and MS, with special assistance of spin system simulation studies for the assignment of an E geometry at C8 in 2. As metabolites of microbes, compounds 1 and 2 are unprecedented in terms of bearing a 2,4-dienone system. Both 1 and 2 showed antibacterial activity against the plant pathogen Rhizobium radiobacter and the fish pathogen Tenacibaculum maritimum, with a contrasting preference that 1 is more effective to the former strain while 2 is so to the latter. In addition, compounds 1 and 2 displayed agonistic activity against peroxisome proliferator-activated receptors (PPARs) with an isoform specificity towards PPARα and PPARγ.
机译:一对几何异构体不饱和酮脂肪酸,(6e,8z) - 和(6e,8e)-5-氧代-6,8-四碳二烯酸(1和2)与放线菌的培养液中分离出来微膜子属,与石珊瑚,Catalaphyllia sp相关联。通过包括NMR和MS的光谱分析阐明了它们的化学结构,具有旋转系统模拟研究的特殊辅助,用于在C8中分配2.作为微生物代谢物,化合物1和2在轴承A 2方面是前所未有的。 ,4-亚酮系统。 1和2均显示抗菌活性对植物病原体根瘤菌的抗菌杆菌和鱼病原体酸纤维素酸纤维素,具有对比的偏好,即1对前一个菌株更有效,而2则为后者。此外,化合物1和2针对过氧化物体增殖物激活的受体(PPAR)的激动活性显示出对PPARα和PPARγ的同种型特异性。

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