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20-Nor-Isopimarane Epimers Produced by Aspergillus wentii SD-310 a Fungal Strain Obtained from Deep Sea Sediment

机译:由深海沉积物获得的真菌菌株aspergillus goii SD-310生产的20-Nor-Isopimaraneane差向异构体

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摘要

Four new uncommon 20-nor-isopimarane diterpenoid epimers, aspewentins I−L (>1–>4), together with a new methylated derivative of >3, aspewentin M (>5), were isolated from the deep sea sediment-derived fungus Aspergillus wentii SD-310. The very similar structures of these epimers made the separation and purification procedures difficult. The structures of compounds >1–>5 were illustrated based on spectroscopic analysis, and the absolute configurations of compounds >1–>5 were unambiguously determined by the combination of NOESY, time-dependent density functional (TDDFT)-ECD calculations, and X-ray crystallographic analysis. These metabolites represented the rare examples of 20-nor-isopimarane analogues possessing a cyclohexa-2,5-dien-1-one moiety. These compounds were tested for antimicrobial activities against human and aquatic pathogenic bacteria, as well as plant-pathogenic fungi. While compounds >1 and >2 exhibited inhibitory activities against zoonotic pathogenic bacteria such as Escherichia coli, Edwardsiella tarda, Vibrio harveyi, and V. parahaemolyticus, compound >5 showed potent activity against the plant pathogen Fusarium graminearum.
机译:四种新的不常见的20-nor-isopimarane二萜类差向异构体,天冬氨酸I-L(> 1 – > 4 ),以及新的> 3 甲基化衍生物从深海沉积物衍生的真菌曲霉曲霉SD-310中分离出了阿斯波温汀M(> 5 )。这些差向异构体的非常相似的结构使分离和纯化过程变得困难。通过光谱分析说明了化合物> 1 – > 5 的结构,化合物> 1 – > 5 由NOESY,随时间变化的密度泛函(TDDFT)-ECD计算和X射线晶体学分析相结合确定。这些代谢物代表了具有环己2,5-dien-1-one部分的20-nor-isopimarane类似物的罕见实例。测试了这些化合物对人和水生病原细菌以及植物致病真菌的抗菌活性。化合物> 1 和> 2 表现出对人畜共患病原性细菌(如大肠杆菌,塔氏爱德华氏菌,哈维氏弧菌和副溶血弧菌)的抑制活性,化合物> 5 对植物病原体禾谷镰刀菌显示出有效的活性。

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