石藻内生黄曲霉代谢物的抑菌活性及核磁共振研究。

Q1 Agricultural and Biological Sciences
Abdel Nasser B Singab, Yasmin A Elkhawas, Eman Al-Sayed, Ahmed M Elissawy, Iten M Fawzy, Nada M Mostafa
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引用次数: 1

摘要

背景:内生曲霉产生无数有价值的生物活性次生代谢物。本研究对软珊瑚中黄曲霉的一种内生菌进行了化学探索,并对其提取的植物成分进行了抑菌活性评价。这是通过使用核磁共振(NMR)光谱学和计算技术来完成的。此外,还研究了黄芪总提取物对乳腺癌细胞(MCF-7)的体外抗癌作用。结果:从内生真菌黄曲霉粗醇提取物中分离得到6个化合物,其中无水美伐内酯为首次报道。对两种不同化合物(Scopularides A和B)的抗真菌和抗幽门螺杆菌性能进行了评估。此外,还进行了计算研究,以确定所有化合物的结合机制。两种化合物对幽门螺杆菌均有抑制作用,最小抑制浓度(MIC)值为7.81 ~ 15.63µg/ mL,克拉霉素为1.95µg/ mL。scopscopides A对白色念珠菌和黑曲霉均有抑制作用,MIC值为3.9 ~ 31.25µg/ mL, scopscopides B仅对白色念珠菌有抑制作用,MIC值为15.63µg/ mL,对黑曲霉的抑制作用较弱(MIC = 125µg/ mL)。此外,对MCF-7细胞具有显著的细胞毒活性(IC50: 30.46 mg/mL)。结论:黄曲霉的细胞毒活性和分子对接支持其抗菌活性,是一种很有前景的潜在抗菌药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Antimicrobial activities of metabolites isolated from endophytic Aspergillus flavus of Sarcophyton ehrenbergi supported by in-silico study and NMR spectroscopy.

Antimicrobial activities of metabolites isolated from endophytic Aspergillus flavus of Sarcophyton ehrenbergi supported by in-silico study and NMR spectroscopy.

Antimicrobial activities of metabolites isolated from endophytic Aspergillus flavus of Sarcophyton ehrenbergi supported by in-silico study and NMR spectroscopy.

Antimicrobial activities of metabolites isolated from endophytic Aspergillus flavus of Sarcophyton ehrenbergi supported by in-silico study and NMR spectroscopy.

Background: Endophytic Aspergillus species produce countless valuable bioactive secondary metabolites. In the current study, Aspergillus flavus an endophyte from the soft coral Sarcophyton ehrenbergi was chemically explored and the extracted phytoconstituents were subsequently evaluated for antimicrobial activity. This is accomplished by employing nuclear magnetic resonance (NMR) spectroscopy and computational techniques. Additionally, An in vitro anticancer analysis of A. flavus total extract against breast cancer cells (MCF-7) was investigated.

Result: Six compounds were separated from the crude alcohol extract of the endophytic Aspergillus flavus out of which anhydro-mevalonolactone was reported for the first time. The anti-fungal and anti-Helicobacter pylori properties of two distinct compounds (Scopularides A and B) were assessed. Additionally, computational research was done to identify the binding mechanisms for all compounds. Both the compounds were found to be active against H. pylori with minimum inhibitory concentration (MIC) values ranging from 7.81 to 15.63 µg/ mL as compared with clarithromycin 1.95 µg/ mL. Scopularides A was potent against both Candida albicans and Aspergillus niger with MIC values ranging from 3.9 to 31.25 µg/ mL, while scopularides B only inhibits Candida albicans with MIC value of 15.63 µg/ mL and weak inhibitory activity against A. niger (MIC = 125 µg/ mL). Furthermore, cytotoxic activity showed a significant effect (IC50: 30.46 mg/mL) against MCF-7 cells.

Conclusion: Our findings report that cytotoxic activity and molecular docking support the antimicrobial activity of Aspergillus flavus, which could be a promising alternative source as a potential antimicrobial agent.

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来源期刊
Fungal Biology and Biotechnology
Fungal Biology and Biotechnology Agricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
10.20
自引率
0.00%
发文量
17
审稿时长
9 weeks
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