J Nat Prod. 2021 Dec 24;84(12):3064-3070. doi: 10.1021/acs.jnatprod.1c00791. Epub 2021 Dec 1.
In 2017 we reported the isolation and characterization of berkeleylactones A-H and A26771B from a coculture of two extremophilic sp. isolated from an acid mine waste lake. Berkeleylactone A exhibited potent activity against several strains of multi-drug-resistant and . A26771B, which is related to the berkeleylactones, also exhibited antibiotic activity. Although the berkeleylactones were novel compounds, A26771B was originally isolated by scientists at Eli Lilly Company from and reported in1977. We recently obtained and grew it in axenic culture. We isolated five new berkeleylactones ( and -), two berkeley-γ-lactones ( and ), and citreohybriddional (), as well as the known compounds A26771B (), berkeleylactone E (), and gliovictin. The structures of the novel compounds were deduced from analysis of spectral data. Compounds and - are 16-membered macrolides, while and are γ-lactones that share the hexadecanoic acid skeleton. A26771B () and berkeleylactone I () were active against several strains of , including four multi-drug-resistant strains. Berkeleylactone N () was active only against .
2017 年,我们从嗜酸极端微生物 sp. 的共培养物中分离并鉴定了伯克利内酯 A-H 和 A26771B。伯克利内酯 A 对几种多药耐药 和 菌株具有很强的活性。与伯克利内酯有关的 A26771B 也具有抗生素活性。虽然伯克利内酯是新型化合物,但 A26771B 最初是由 Eli Lilly 公司的科学家从 中分离出来的,并于 1977 年报道。我们最近获得了 和并在无菌培养中进行了培养。我们分离出了五种新的伯克利内酯(、-)、两种伯克利γ-内酯(、)和 citreohybriddional(),以及已知的化合物 A26771B()、伯克利内酯 E()和 gliovictin。新化合物的结构是通过分析光谱数据推断出来的。化合物 和 - 是 16 元大环内酯,而 和 是共享十六烷酸骨架的γ-内酯。A26771B()和伯克利内酯 I()对包括四种多药耐药株在内的几种 菌株具有活性。伯克利内酯 N()仅对 菌株有效。