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萨普霉素 A-E,新型安格洛环素抗生素,对寄生腐霉有活性。

Saprolmycins A-E, new angucycline antibiotics active against Saprolegnia parasitica.

机构信息

Graduate School of Science and Engineering, Ritsumeikan University, Kusatsu, Shiga, Japan.

出版信息

J Antibiot (Tokyo). 2012 Dec;65(12):599-607. doi: 10.1038/ja.2012.86. Epub 2012 Oct 24.

Abstract

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.

摘要

从链霉菌 TK08046 的发酵液中分离到 5 种新的抗寄生植物单胞菌抗生素 saprolmycins A-E。通过 NMR 和光谱分析相结合的方法,确定了这些化合物的结构为一组与 saquayamycin 密切相关的新型蒽环类化合物。Saprolmycin A 和 E 对寄生植物单胞菌表现出很强的选择性抑制活性,MIC 值分别为 3.9 和 7.8 ng/ml,但对真菌、革兰氏阳性或阴性菌、微藻或浮游动物几乎没有或没有活性。我们的研究结果表明这两种化合物是非常有效和环境安全的抗寄生植物单胞菌候选药物。

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