菖蒲叶内生真菌Xylaria ellisii的非靶向代谢组学及生物活性评价

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY Current pharmaceutical design Pub Date : 2025-01-01 DOI:10.2174/0113816128337697250106001808
Chandrabhan Prajapati, Sachchida Nand Rai, Anurag Kumar Singh, Naina Rajak, Neha Garg, Santosh Kumar Singh
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引用次数: 0

摘要

真菌内生菌与植物寄主有互惠关系,通过遗传和代谢过程进行交流。因此,它们获得了产生具有治疗效果的代谢物及其衍生物的能力。方法:本研究旨在评估从菖蒲叶组织中分离的强效内生真菌Xylaria ellisii粗提物的抗氧化潜力,并鉴定其代谢产物。从菖蒲叶组织中分离得到4种内生真菌。在形态和分子上被鉴定为不同的物种。各乙酸乙酯提取物在不同波长的HPTLC指纹图谱中表现出独特的化学特征。真菌ACL-4 (Xylaria ellisii)的乙酸乙酯(EA)提取物的抗氧化活性最强,EC50值为292.64±3.558 μg/mL。真菌内生菌ACL-4提取物在较低浓度下的抑菌活性明显优于叶片粗提物ACL-ME提取物。结果:与真菌菌株acl -4处理HEK 293T细胞的IC50值> 2000 μg/mL相比,acl - me处理HEK 293T细胞提取物具有明显的毒性,IC50值为1481.74±23.772 μg/mL。结果表明,ACL-4粗提物和ACL-ME与标准药物甲氨蝶呤对肿瘤细胞株MDA-MB-231的IC50浓度分别为146.65±0.394 μg/mL、528.46±10.912 μg/mL和134.11±3.446 μg/mL。基于lc - hrms的代谢组学方法在木霉粗代谢物中共检测到2255个化合物,其中某些化合物在多个实例中被鉴定出来。在现有文献的指导下,通过精心筛选,鉴定出62种强大的生物活性化合物。通过对比hplc指纹图谱分析,以及从菖蒲叶和决明子枝中提取的木霉乙酸乙酯提取物的抗氧化活性测定,揭示了木霉产生的生物活性物质对宿主的特异性。结论:从木耳中提取的Keap1抑制剂评分最高,分别为普瑞巴林(-6.083 Kcal/mol)、阿威酸(-5.434 Kcal/mol)、(R)-哌啶-2-羧酸(-5.31 Kcal/mol)、吉尼平(-5.197 Kcal/mol)和布瓦西坦(-5.17 Kcal/mol),均可作为Keap1抑制剂。
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Untargeted Metabolomics and Bioactivities Assessment of Xylaria ellisii, an Endophytic Fungus Isolated from the Leaf of the Plant Acorus calamus Linn.

Introduction: Fungal endophytes have mutualistic associations with the plant's host, communicating through genetic and metabolic processes. As a result, they gain the ability to generate therapeutically effective metabolites and their derivatives.

Methods: The current study aims to assess antioxidant potential along with the identification of robust metabolites within the crude extract of a potent endophytic fungus Xylaria ellisii isolated from leaf tissues of the Acorus calamus Linn. plant. Four endophytic fungi were obtained from leaf tissues of Acorus calamus Linn., and identified morphologically and molecularly as distinct species. Each ethyl acetate extract of the isolated fungi exhibited a unique chemical profile in the HPTLC fingerprint at various wavelengths. The ethyl acetate (EA) extract from the fungal strain ACL-4 (Xylaria ellisii) demonstrated the strongest antioxidant activity among the four fungal endophytes examined, with an EC50 value of 292.64 ± 3.558 μg/mL. Remarkably, fungal endophyte ACL-4 extract exhibited superior antimicrobial activity at the less concentrations compared to ACL-ME extract of leaf crude.

Results: The extract of ACL-ME-treated HEK 293T cells exhibited significant toxicity, with an IC50 value of 1481.74 ± 23.772 μg/mL, compared to fungal strain ACL-4-treated HEK 293T cells, which had an IC50 value greater than 2000 μg/mL. Consequently, the crude extract of ACL-4 and ACL-ME along with the standard drug methotrexate exhibited cytotoxic activity against cancer cell line MDA-MB-231 with IC50 concentrations of 146.65 ± 0.394 μg/mL, 528.46 ± 10.912 μg/mL, and 134.11 ± 3.446 μg/mL, respectively. A total of 2,255 compounds were detected through LC-HRMS-based metabolomics in the crude metabolites of Xylaria ellisii, with certain compounds identified in multiple instances. Among this repertoire, 62 robust bioactive compounds were identified through meticulous screening, guided by existing literature. Comparative HPTLC fingerprint analysis, along with antioxidant efficacy assays of ethyl acetate extracts of Xylaria ellisii derived from Acorus calamus leaves and Cassia fistula twigs revealed the host-specific production of bioactive chemicals.

Conclusion: The top-scoring Keap1 inhibitors derived from Xylaria ellisii, including Pregabalin (-6.083 Kcal/mol), Ferulic acid (-5.434 Kcal/mol), (R)-Piperidine-2-carboxylic acid (-5.31 Kcal/mol), Genipin (-5.197 Kcal/mol), and Brivaracetam (-5.17 Kcal/mol), respectively were considered as Keap 1 inhibitors, potentially mitigate oxidative stress.

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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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