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体外和计算机模拟研究废咖啡生物活性酚类物质作为一种有前途的黄曲霉毒素生产抑制剂。

In-Vitro and In-Silico Investigation for the Spent-Coffee Bioactive Phenolics as a Promising Aflatoxins Production Inhibitor.

机构信息

Flavor and Aroma Chemistry Department, National Research Centre, Dokki, Cairo 12622, Egypt.

Food Science & Nutrition Department, College of Food and Agricultural Sciences, King Saud University, Riyadh 11451, Saudi Arabia.

出版信息

Toxins (Basel). 2023 Mar 16;15(3):225. doi: 10.3390/toxins15030225.

Abstract

Aflatoxin, is a naturally occurring polyketide generated by via biosynthetic pathways, including polyketide synthase (PKS) and non-ribosomal enzymes. The in vitro analysis supported by molecular dynamics (MD) techniques was used to examine the antifungal and anti-aflatoxigenic activity of spent coffee grounds (SCGs) methanol extract. The High-Performance Liquid Chromatography results revealed the presence of 15 phenolic acids and five flavonoids. (R)-(+)-Rosmarinic acid (176.43 ± 2.41 µg/g) was the predominant of the detected acids, followed by gallic acid (34.83 ± 1.05 µg/g). At the same time, apigenin-7-glucoside is the dominant flavonoid in the SCGs extract by 1717.05 ± 5.76 µg/g, and naringin (97.27 ± 1.97 µg/g) comes next. The antifungal and anti-aflatoxigenic activity of the SCGs extracts was 380 µL/mL and 460 µL/mL, respectively. The SGGs' effect of inhibiting five strains' growth on the agar media ranged between 12.81 ± 1.71 to 15.64 ± 1.08 mm by two diffusion assays. Molecular docking results confirmed the inhibitory action of different phenolics and flavonoids on the PKS and NPS key enzymes of the aflatoxin biosynthetic mechanism. The SCGs extract components with the highest free binding energy, naringin (-9.1 kcal/mL) and apigenin 7-glucoside (-9.1 kcal/mol), were subjected to an MD simulation study. The computational results infer the stabilizing effects on the enzymes upon ligand binding led to the impairment in its functionality. The current study represents a novel attempt to assess the anti aflatoxins mechanism of phenolics and flavonoids targeting PKS and NPS via computational approaches compared to in-vitro assays.

摘要

黄曲霉毒素是一种天然存在的多酮类化合物,由曲霉属通过生物合成途径生成,包括聚酮合酶(PKS)和非核糖体酶。通过分子动力学(MD)技术支持的体外分析用于检查废咖啡渣(SCG)甲醇提取物的抗真菌和抗黄曲霉毒素活性。高效液相色谱结果显示存在 15 种酚酸和 5 种类黄酮。(R)-(+)-迷迭香酸(176.43 ± 2.41 µg/g)是检测到的酸中的主要成分,其次是没食子酸(34.83 ± 1.05 µg/g)。同时,在 SCGs 提取物中,芹菜素-7-葡萄糖苷是主要的类黄酮,含量为 1717.05 ± 5.76 µg/g,其次是柚皮苷(97.27 ± 1.97 µg/g)。SCGs 提取物的抗真菌和抗黄曲霉毒素活性分别为 380 µL/mL 和 460 µL/mL。通过两种扩散试验,SGGs 对五种曲霉属菌株在琼脂培养基上生长的抑制作用范围在 12.81 ± 1.71 至 15.64 ± 1.08 mm 之间。分子对接结果证实了不同酚类和类黄酮对黄曲霉毒素生物合成机制中 PKS 和 NPS 关键酶的抑制作用。具有最高游离结合能的 SCGs 提取物成分,柚皮苷(-9.1 kcal/mL)和芹菜素 7-葡萄糖苷(-9.1 kcal/mol),进行了 MD 模拟研究。计算结果推断出配体结合导致酶的稳定作用,从而使其功能受损。与体外测定相比,本研究代表了通过计算方法评估针对 PKS 和 NPS 的酚类和类黄酮的抗黄曲霉毒素机制的新尝试。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1fa/10051990/90aa7e71a90b/toxins-15-00225-g001.jpg

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