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三种海洋来源菌株培养物中的新型 Phocoenamicin 和 Maklamicin 类似物。

New Phocoenamicin and Maklamicin Analogues from Cultures of Three Marine-Derived Strains.

机构信息

Fundación MEDINA, Centro de Excelencia en Investigación de Medicamentos Innovadores en Andalucía, Parque Tecnológico Ciencias de la Salud, Avda. del Conocimiento 34, Armilla, 18016 Granada, Spain.

Laboratory for Molecular Biodiscovery, Department of Pharmaceutical and Pharmacological Sciences, University of Leuven, O & N II Herestraat 49-box 824, 3000 Leuven, Belgium.

出版信息

Mar Drugs. 2023 Aug 7;21(8):443. doi: 10.3390/md21080443.

Abstract

Antimicrobial resistance can be considered a hidden global pandemic and research must be reinforced for the discovery of new antibiotics. The spirotetronate class of polyketides, with more than 100 bioactive compounds described to date, has recently grown with the discovery of phocoenamicins, compounds displaying different antibiotic activities. Three marine strains (CA-214671, CA-214658 and CA-218877), identified as phocoenamicins producers, were chosen to scale up their production and LC/HRMS analyses proved that EtOAc extracts from their culture broths produce several structurally related compounds not disclosed before. Herein, we report the production, isolation and structural elucidation of two new phocoenamicins, phocoenamicins D and E (-), along with the known phocoenamicin, phocoenamicins B and C (-), as well as maklamicin () and maklamicin B (), the latter being reported for the first time as a natural product. All the isolated compounds were tested against various human pathogens and revealed diverse strong to negligible activity against methicillin-resistant , H37Ra, and . Their cell viability was also evaluated against the human liver adenocarcinoma cell line (Hep G2), demonstrating weak or no cytotoxicity. Lastly, the safety of the major compounds obtained, phocoenamicin (), phocoenamicin B () and maklamicin (), was tested against zebrafish eleuthero embryos and all of them displayed no toxicity up to a concentration of 25 μM.

摘要

抗微生物药物耐药性可以被视为一种隐形的全球大流行病,必须加强研究以发现新的抗生素。螺缩酮类聚酮化合物,迄今为止已有 100 多种具有生物活性的化合物被描述,随着 phocoenamicin 的发现,其种类最近有所增加,这些化合物具有不同的抗生素活性。选择了三种海洋菌株(CA-214671、CA-214658 和 CA-218877)进行扩大生产,LC/HRMS 分析证明,它们的培养物肉汤的 EtOAc 提取物产生了几种以前未披露的结构相关化合物。在此,我们报告了两种新的 phocoenamicin(phocoenamicin D 和 E(-))的生产、分离和结构阐明,以及已知的 phocoenamicin(phocoenamicin B 和 C(-))以及 maklamicin()和 maklamicin B(),后者首次被报道为天然产物。所有分离出的化合物都针对各种人类病原体进行了测试,结果显示对耐甲氧西林金黄色葡萄球菌、H37Ra 和 具有不同程度的强至可忽略的活性。它们的细胞活力也针对人肝癌细胞系(Hep G2)进行了评估,结果表明它们的细胞活力对 Hep G2 具有弱毒性或无毒性。最后,对获得的主要化合物 phocoenamicin()、phocoenamicin B()和 maklamicin()的安全性进行了测试,结果表明它们在高达 25 μM 的浓度下对斑马鱼幼鱼没有毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a7e/10455904/0a848a4b7aff/marinedrugs-21-00443-g001.jpg

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