黄芩端裂菌(Teloschistes flavicans)的地衣物质诺曼:它们的分离、晶体结构和抗菌活性的评价。

Narra J Pub Date : 2025-08-01 Epub Date: 2025-04-23 DOI:10.52225/narra.v5i2.1463
Friardi Ismed, Nurwahidatul Arifa, Mentari Q Nissa, Deddi P Putra, Analia Ic Orue, Jack K Clegg, Isabelle Rouaud, L Dévéhat Françoise
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引用次数: 0

摘要

黄斑端裂鱼(Sw.)诺曼地衣是一种被称为金毛地衣的地衣。这种地衣已被公认并用于草药混合物中,作为一种抗微生物物质和在生态系统中发挥作用的空气污染生物指示剂。本研究的目的是探索其次级代谢物作为抗菌和抗癌剂的潜力,特别是对细菌性肺炎。用色谱法分离得到了两个主要化合物vicacinin和parietin,并用光谱法和x射线单晶衍射法对其进行了鉴定。本文首次报道了维卡尼辛的结晶学数据。用色谱法和重结晶法分别获得了桔黄色晶体(parietin)和白色晶体(vicanicin)。此外,研究了这些化合物对角质形成细胞(HaCaT)细胞的细胞毒性和对肺炎病原体(肺炎克雷伯菌ATCC 1706、肺炎链球菌ATCC 49619、卡他莫拉菌ATCC 25240和化脓性葡萄球菌ATCC 19615)的抗菌活性。在50 ~ 100µM浓度下,这些化合物的细胞毒活性适中。与氯霉素相比,其抗菌肺炎活性相对较弱。在这两种化合物中,维卡尼辛对所有菌株的活性都强于帕耶丁。维卡尼辛对肺炎克雷伯菌和化脓性葡萄球菌的抑制作用较强,最低抑制浓度分别为156±0.77µM和156±0.91µM。本研究成功地阐明了parietin和vicanicin的完整分子结构,并提供了它们的抗菌和细胞毒活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Lichen substances from <i>Teloschistes flavicans</i> (Sw.) Norman: Isolation, crystal structure, and evaluation of their antibacterial activities.

Lichen substances from <i>Teloschistes flavicans</i> (Sw.) Norman: Isolation, crystal structure, and evaluation of their antibacterial activities.

Lichen substances from <i>Teloschistes flavicans</i> (Sw.) Norman: Isolation, crystal structure, and evaluation of their antibacterial activities.

Lichen substances from Teloschistes flavicans (Sw.) Norman: Isolation, crystal structure, and evaluation of their antibacterial activities.

Teloschistes flavicans (Sw.) Norman is a lichen known as the golden-haired lichen. This lichen has been recognized and used in herbal medicine mixtures as an antimicrobial and bioindicator of air pollution that plays a role in ecological systems. The aim of this study was to explore the potential of its secondary metabolites as antibacterial and anticancer agents, particularly against bacterial pneumonia. Two main compounds (vicacinin and parietin) were isolated with chromatography and identified by spectrometry and single- crystal X-ray diffraction. The crystallographic data of vicanicin are reported for the first time. Chromatography and recrystallization methods were used to obtain both compounds with orange (parietin) and white (vicanicin) crystals. Furthermore, these compounds were evaluated for cytotoxicity on keratinocytes (HaCaT) cells and antibacterial activity against pneumonia pathogens (Klebsiella pneumoniae ATCC 1706, Streptococcus pneumoniae ATCC 49619, Moraxella catarhalis ATCC 25240, and Staphylococcus pyogenes ATCC 19615). The cytotoxic activity of these compounds was moderate at the concentration of 50-100 µM. The antibacterial pneumonia activity was relatively weak compared to chloramphenicol. Between the two compounds, vicanicin showed stronger activity than parietin against all strains. Vicanicin was more active against Klebsiella pneumoniae and Staphylococcus pyogenes with minimum inhibitory concentrations of 156±0.77 µM and 156±0.91 µM, respectively. In this study, comprehensive molecular structures of parietin and vicanicin have been successfully elucidated, and their antibacterial and cytotoxic activities have been provided.

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