Jouda Jean-Bosco, Kusari Souvik, Lamshöft Marc, Mouafo Talontsi Ferdinand, Douala Meli Clovis, Wandji Jean, Spiteller Michael
Institute of Environmental Research (INFU), Department of Chemistry and Chemical Biology, TU Dortmund, Otto-Hahn-Str. 6, D-44221 Dortmund, Germany; Department of Organic Chemistry, Faculty of Science, University of Yaoundé 1, P.O. Box 812, Yaoundé, Cameroon.
Institute of Environmental Research (INFU), Department of Chemistry and Chemical Biology, TU Dortmund, Otto-Hahn-Str. 6, D-44221 Dortmund, Germany.
Fitoterapia. 2014 Oct;98:209-14. doi: 10.1016/j.fitote.2014.08.011. Epub 2014 Aug 12.
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 HRMS(n)). 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 coli. 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 1.
从喀麦隆药用植物诺氏藤黄叶片中内生真菌青霉属(Penicillium sp.)分离得到三种新的聚酮化合物,命名为阴茎菌素A - C(1 - 3),以及一种已知化合物柠檬菌素(4)。通过光谱和波谱方法(核磁共振和高分辨质谱(n))阐明了它们的结构。测试了新化合物(1 - 3)对临床上重要的风险组2(RG2)金黄色葡萄球菌和大肠杆菌菌株的抗菌效果。测定中还包括生态上具有重要意义的大肠杆菌(RG1)、枯草芽孢杆菌和不动杆菌属BD4菌株。化合物3对临床相关的金黄色葡萄球菌以及枯草芽孢杆菌表现出显著活性,与参考标准品(链霉素)相当。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处的取代基可显著提高1的抗菌活性。