首页> 外文期刊>The Journal of Antibiotics: An International Journal >Saprolmycins A-E, new angucycline antibiotics active against Saprolegnia parasitica
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Saprolmycins A-E, new angucycline antibiotics active against Saprolegnia parasitica

机译:Saprolmycins A-E,新的洋环霉素抗生素,对寄生腐烂腐烂症有活性

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Saprolmycins A-E, five new anti-Saprolegnia parasitica antibiotics were isolated from the culture broth of Streptomyces sp. strain TK08046. As determined using a combination of NMR and spectroscopic analyses, the structures of these compounds were elucidated as a new group of angucycline compounds closely related to saquayamycin. Saprolmycin A and E exhibited potent anti-S. parasitica selective activities, with MIC values of 3.9 and 7.8 ng ml-1, respectively, but weak or no activity against fungi, gram-positive or-negative bacteria, and microalgae or zooplankton. Our results suggest these two compounds as highly effective and environmentally safe anti-saprolegniasis candidates.
机译:从链霉菌属菌种的培养液中分离出了五种新的抗霉素类新霉素:Saprolmyss A-E。菌株TK08046。如结合NMR和光谱分析所确定的,这些化合物的结构被阐明为一组与sa霉素密切相关的安古环素化合物。 Saprolmycin A和E表现出强大的抗S活性。寄生虫的选择性活性,MIC值分别为3.9和7.8 ng ml-1,但对真菌,革兰氏阳性或阴性细菌以及微藻类或浮游动物的活性较弱或没有活性。我们的结果表明这两种化合物是高效和对环境安全的抗腐烂症的候选药物。

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