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Penialidins A-C with strong antibacterial activities from Penicillium sp., an endophytic fungus harboring leaves of Garcinia nobilis

机译:Penialidins A-C具有青霉菌(Penicillium sp。)的强抗菌活性,Penicillium sp。是带有藤黄藤本植物叶子的内生真菌

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摘要

Three new polyketides named penialidins A-C (1-3), along with one known compound, citromycetin (4), were isolated from an endophytic fungus, Penicillium sp., harbored in the leaves of the Cameroonian medicinal plant Garcinia nobilis. Their structures were elucidated by means of spectroscopic and spectrometric methods (NMR and HRMSn). The antibacterial efficacies of the new compounds (1-3) were tested against the clinically-important risk group 2 (RG2) bacterial strains of Staphylococcus aureus and Escherichia coll. The ecologically imposing strains of E. coli (RG1), Bacillus subtilis and Acinetobacter sp. BD4 were also included in the assay. Compound 3 exhibited pronounced activity against the clinically-relevant S. aureus as well as against B. subtilis comparable to that of the reference standard (streptomycin). Compound 2 was also highly-active against S. aureus. By comparing the structures of the three new compounds (1-3), it was revealed that altering the substitutions at C-10 and C-2 can significantly increase the antibacterial activity of I
机译:从喀麦隆药用植物加拿大藤黄的叶子中的内生真菌Penicillium sp。中分离出了三种新的称为酮化合物A-C(1-3)的聚酮化合物以及一种已知的化合物柠檬霉素(4)。通过光谱和光谱方法(NMR和HRMSn)阐明了它们的结构。测试了新化合物(1-3)的抗金黄色葡萄球菌和大肠埃希氏菌临床上重要的危险组2(RG2)细菌菌株的抗菌效果。具有生态影响的大肠杆菌(RG1),枯草芽孢杆菌和不动杆菌属菌株。 BD4也包括在测定中。化合物3对临床相关的金黄色葡萄球菌和枯草芽孢杆菌均具有与参考标准(链霉素)相当的活性。化合物2对金黄色葡萄球菌也具有高活性。通过比较三种新化合物(1-3)的结构,发现改变C-10和C-2的取代基可以显着提高I的抗菌活性。

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