Gräfe U, Schlegel R, Ritzau M, Ihn W, Dornberger K, Stengel C, Fleck W F, Gutsche W, Härtl A, Paulus E F
Hans-Knöll-Institute of Natural Product Research, Jena, Germany.
J Antibiot (Tokyo). 1995 Feb;48(2):119-25. doi: 10.7164/antibiotics.48.119.
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.
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。