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Chemical Diversity of Polyene Macrolides Produced by Streptomyces noursei ATCC 11455 and Recombinant Strain ERD44 with Genetically Altered Polyketide Synthase NysC

机译:链霉菌ATCC 11455和重组菌株ERD44与转基因聚酮化合物合酶NysC产生的多烯大环内酯类化合物的化学多样性

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摘要

The gram-positive bacterium Streptomyces noursei ATCC 11455 produces a complex mixture of polyene macrolides generally termed nystatins. Although the structures for nystatins A1 and A3 have been reported, the identities of other components of the nystatin complex remain obscure. Analyses of the culture extract from the S. noursei wild type revealed the presence of several nystatin-related compounds for which chemical structures could be suggested on the basis of their molecular weights, their UV spectra, and knowledge of the nystatin biosynthetic pathway. Nuclear magnetic resonance (NMR) studies with one of these polyene macrolides identified it as a nystatin analogue containing a mycarose moiety at C-35. A similar investigation was performed with the culture extract of the ERD44 mutant, which has a genetically altered polyketide synthase (PKS) NysC and which was previously shown to produce a heptaene nystatin analogue. The latter compound, tentatively named S44HP, and its derivative, which contains two deoxysugar moieties, were purified; and their structures were confirmed by NMR analysis. Nystatin analogues with an expanded macrolactone ring were also observed in the extract of the ERD44 mutant, suggesting that the altered PKS can “stutter” during the polyketide chain assembly. These data provide new insights into the biosynthesis of polyene macrolide antibiotics and the functionalities of PKSs and post-PKS modification enzymes.
机译:革兰氏阳性细菌努氏链霉菌ATCC 11455产生了多烯大环内酯类化合物的复杂混合物,通常称为制霉菌素。尽管制霉菌素A1和A3的结构已有报道,但制霉菌素复合物其他成分的身份仍然不清楚。对来自野生链霉菌野生型的培养物提取物的分析显示,存在几种制霉菌素相关化合物,可以根据其分子量,紫外光谱和制霉菌素生物合成途径的知识来建议其化学结构。使用这些多烯大环内酯类之一的核磁共振(NMR)研究将其鉴定为制霉菌素类似物,其在C-35处含有霉菌糖部分。对ERD44突变体的培养物提取物进行了类似的研究,该突变体具有基因改变的聚酮化合物合酶(PKS)NysC,以前已证明可产生七烯制霉菌素类似物。纯化了后一种化合物(暂定名为S44HP)及其衍生物,其中包含两个脱氧糖部分;并通过NMR分析证实其结构。在ERD44突变体的提取物中还观察到具有扩大的大内酯环的制霉菌素类似物,表明改变的PKS可能在聚酮化合物链组装过程中“口吃”。这些数据为多烯大环内酯类抗生素的生物合成以及PKS和后PKS修饰酶的功能提供了新的见识。

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