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橙霉素,来自橙色链霉菌IMET 43917的新型缩肽抗生素。生产、分离、结构解析及生物活性

Aurantimycins, new depsipeptide antibiotics from Streptomyces aurantiacus IMET 43917. Production, isolation, structure elucidation, and biological activity.

作者信息

Gräfe U, Schlegel R, Ritzau M, Ihn W, Dornberger K, Stengel C, Fleck W F, Gutsche W, Härtl A, Paulus E F

机构信息

Hans-Knöll-Institute of Natural Product Research, Jena, Germany.

出版信息

J Antibiot (Tokyo). 1995 Feb;48(2):119-25. doi: 10.7164/antibiotics.48.119.

Abstract

Aurantimycins A (1), B (2) and C (3) were isolated from the mycelium of Streptomyces aurantiacus JA 4570 as new representatives of the azinothricin group of hexadepsipeptide antibiotics. Their structures were settled by X-ray diffraction analysis of crystalline aurantimycin A (1), high field homo- and heteronuclear 2D NMR experiments, high-resolution mass spectrometry and amino acid analysis. Aurantimycins are characterized by a new side chain containing fourteen carbon atoms. They display strong activity against Gram-positive bacteria and cytotoxic effects against L-929 mouse fibroblast cells.

摘要

橙霉素A(1)、B(2)和C(3)是从橙色链霉菌JA 4570的菌丝体中分离得到的,它们是六缩肽抗生素叠氮丝氨酸组的新成员。通过对结晶橙霉素A(1)进行X射线衍射分析、高场同核和异核二维核磁共振实验、高分辨率质谱分析以及氨基酸分析确定了它们的结构。橙霉素的特征在于含有14个碳原子的新侧链。它们对革兰氏阳性菌显示出强活性,对L-929小鼠成纤维细胞具有细胞毒性作用。

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