Isolation, structure elucidation, total synthesis, and biosynthesis of dermazolium A, an antibacterial imidazolium metabolite of a vaginal bacterium Dermabacter vaginalis

IF 6.9 3区 医学 Q1 CHEMISTRY, MEDICINAL Archives of Pharmacal Research Pub Date : 2023-01-16 DOI:10.1007/s12272-022-01424-z
Hye Ryeong Kim, Jonghwan Kim, Jae Sik Yu, Bum Soo Lee, Ki Hyun Kim, Chung Sub Kim
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引用次数: 5

Abstract

Dermabacter vaginalis is a human-derived bacterium isolated from vaginal fluid of a Korean female in 2016. Although several human-related species in Dermabacter genus have been reported there are few studies on their bioactive metabolites. Dermazolium A (1), a rare imidazolium metabolite, was isolated from D. vaginalis along with five known metabolites (2–6) and their chemical structures were determined by NMR, HRMS, and MS/MS data analysis. Feeding experiments using predicted precursors and biomimetic total synthesis of 1 corroborated its structure and led to suggestion of biosynthetic pathway of 1. Antibacterial tests on the isolated compounds showed that 1 is a mild antibacterial agent with MIC values of 41 µg/mL against methicillin-resistant Staphylococcus aureus (MRSA) USA300, Lacticaseibacillus paracasei subsp. paracasei KCTC 3510 and Brevibacterium epidermidis KCTC 3090.

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阴道皮杆菌抗菌咪唑代谢物dermazolium A的分离、结构解析、全合成和生物合成
阴道Dermabacter vaginalis是2016年从一名韩国女性阴道液中分离出的一种人类来源的细菌。尽管已经报道了几种Dermabacter属的人类亲缘物种,但对其生物活性代谢产物的研究很少。Dermazolium A(1)是一种罕见的咪唑代谢产物,与五种已知的代谢产物(2-6)一起从阴道D.vaginalis中分离出来,并通过NMR、HRMS和MS/MS数据分析确定了它们的化学结构。使用预测的前体和1的仿生全合成的饲养实验证实了其结构,并提出了1的生物合成途径。对分离化合物的抗菌试验表明,1是一种温和的抗菌剂,对耐甲氧西林金黄色葡萄球菌(MRSA)USA300、副干酪乳杆菌亚种的MIC值为41µg/mL。副酪蛋白KCTC 3510和表皮短杆菌KCTC 3090。
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来源期刊
CiteScore
13.40
自引率
9.00%
发文量
48
审稿时长
3.3 months
期刊介绍: Archives of Pharmacal Research is the official journal of the Pharmaceutical Society of Korea and has been published since 1976. Archives of Pharmacal Research is an interdisciplinary journal devoted to the publication of original scientific research papers and reviews in the fields of drug discovery, drug development, and drug actions with a view to providing fundamental and novel information on drugs and drug candidates.
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