聚酮
立体化学
糖苷
取代基
拉伤
链霉菌
化学
细菌
生物
微生物学
生物化学
基因
遗传学
生物合成
解剖
作者
Kerstin Herold,Friedrich A. Gollmick,Ingrid Groth,Martin Roth,Klaus‐Dieter Menzel,Ute Möllmann,U. Gräfe,Christian Hertweck
标识
DOI:10.1002/chem.200500320
摘要
Cervimycins A-D are novel polyketide glycosides with significant activity against multi-drug-resistant staphylococci and vancomycin-resistant enterococci. They are produced by a strain of Streptomyces tendae, isolated from an ancient cave. The structures of the cervimycins were determined by performing extensive NMR and chemical degradation studies. All cervimycins have a common tetracyclic polyketide core that is substituted with unusual di- and tetrasaccharide chains, composed exclusively of trideoxysugars; however, they differ in the acetyl and carbamoyl ring substituent and in the highly unusual terminal methylmalonyl and dimethylmalonyl residues.
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