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来自 Actinoallomurus 的抗菌顺磁醌

Antibacterial Paramagnetic Quinones from Actinoallomurus.

机构信息

Naicons Srl , Viale Ortles 22/4, 20139 Milano, Italy.

KtedoGen Srl , Viale Ortles 22/4, 20139 Milano, Italy.

出版信息

J Nat Prod. 2017 Apr 28;80(4):819-827. doi: 10.1021/acs.jnatprod.6b00654. Epub 2017 Feb 20.

Abstract

Four metabolites, designated paramagnetoquinone A, B, C, and D (1-4), were isolated from three strains belonging to the actinomycete genus Actinoallomurus. Compounds 1 and 2 showed potent antibacterial activity with MIC values lower than 0.015 μg/mL against Gram-positive pathogens, including antibiotic-resistant strains. Since compounds 1 and 2 were NMR-silent due to the presence of an oxygen radical, structure elucidation was achieved through a combination of derivatizations, oxidations, and analysis of C-labeled compounds. The paramagnetoquinones share the same carbon scaffold as tetracenomycin but carry two quinones and a five-membered lactone fused to the aromatic system. Compounds 2 and 1 are identical except for an unprecedented replacement of a methoxy in 2 by a methylamino group in 1. Related compounds devoid of methyl group(s) and of antibacterial activity were isolated from a different Actinoallomurus strain. The likely pmq biosynthetic gene cluster was identified from strain ID145113. While the cluster encodes many of the expected enzymes involved in the formation of aromatic polyketides, it also encodes a dedicated ketoacid dehydrogenase complex and an unusual acyl carrier protein transacylase, suggesting that an unusual starter unit might prime the polyketide synthase.

摘要

从属于放线菌属的 Actinoallomurus 的三个菌株中分离得到了四个代谢物,分别命名为 paramagnetoquinone A、B、C 和 D(1-4)。化合物 1 和 2 表现出很强的抗菌活性,对革兰氏阳性病原体,包括抗生素耐药株的 MIC 值低于 0.015 μg/mL。由于化合物 1 和 2 由于存在氧自由基而 NMR 信号沉默,因此通过衍生化、氧化和分析 C 标记化合物的组合来确定结构。paramagnetoquinones 与 tetracenomycin 具有相同的碳骨架,但在芳香体系上带有两个醌和一个五元内酯。化合物 2 和 1 除了在 1 中用甲氨基取代 2 中的甲氧基外完全相同。从不同的 Actinoallomurus 菌株中分离得到了没有甲基基团且没有抗菌活性的相关化合物。从菌株 ID145113 中鉴定出可能的 pmq 生物合成基因簇。虽然该簇编码了许多形成芳香聚酮的预期酶,但它还编码了一个专用的酮酸脱氢酶复合物和一个不寻常的酰基载体蛋白转酰基酶,这表明一个不寻常的起始单元可能启动聚酮合酶。

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