首页> 外文期刊>European journal of organic chemistry >Secondary Metabolites by Chemical Screening, 41 Structure and Biosynthesis of Mutolide, a Novel Macrolide from a UV Mutant of the Fungus F-24'707
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Secondary Metabolites by Chemical Screening, 41 Structure and Biosynthesis of Mutolide, a Novel Macrolide from a UV Mutant of the Fungus F-24'707

机译:通过化学筛选获得次生代谢产物,穆托利德41的结构和生物合成,穆托利德是真菌F-24'707的紫外线突变体产生的新型大环内酯。

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摘要

The 14-membered macrolide, mutolide (1), was discovered by chemical screening of the culture broth of the fungus F-24'707y, obtained after UV mutagenesis of the wild type strain, which normally produces the spirobisnaphthalene cladospirone bisepoxide (2). The structure of 1 was established by detailed spectroscopic analysis, X-ray analysis and derivatisation. The biogenetic origin of the carbon skeleton and the hydroxy groups was verified by feeding sodium [1-~(13)C]-acetate and ~(18)O_2 to growing cultures of the fungus. Macrolide 1 is generated from acetate/malonate only. The unexpected change of the normal metabolite pattern of this strain is discussed, and proves the value of the OSMAC method.
机译:通过对真菌F-24'707y的培养液进行化学筛选,发现了14元大环内酯多杀菌素(1),该菌是在野生型菌株经紫外线诱变后获得的,该菌株通常会产生螺双萘萘基双螺旋环氧化物(2)。 1的结构通过详细的光谱分析,X射线分析和衍生化确定。通过将[1-〜(13)C]-乙酸钠和〜(18)O_2加到真菌的生长培养物中来验证碳骨架和羟基的生物遗传起源。大环内酯1仅由乙酸盐/丙二酸盐生成。讨论了该菌株正常代谢物模式的意外变化,并证明了OSMAC方法的价值。

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