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L.亚种Falezlez的生物活性酚类物质:抗氧化和脲酶抑制活性的分子与生化研究方法

Bioactive Phenolics of L. Subsp. Falezlez: A Molecular and Biochemical Approach to Antioxidant and Urease Inhibitory Activities.

作者信息

Lekmine Sabrina, Benslama Ouided, Bensalah Bachir, Touzout Nabil, Moussa Hamza, Tahraoui Hichem, Ola Mohammad Shamsul, Hafsa Haroun, Zhang Jie, Amrane Abdeltif

机构信息

Biotechnology, Water, Environment and Health Laboratory, Abbes Laghrour University, Khenchela 40000, Algeria.

Laboratory of Natural Substances, Biomolecules, and Biotechnological Applications, Department of Natural and Life Sciences, Larbi Ben M'Hidi University, Oum El Bouaghi 04000, Algeria.

出版信息

Int J Mol Sci. 2025 Jan 4;26(1):370. doi: 10.3390/ijms26010370.

Abstract

This study examines the chemical composition, antioxidant properties, and urease inhibitory effects of L. subsp. falezlez (Coss.) Maire. Using LC-ESI-MS/MS, 19 distinct phenolic compounds were identified, with chlorogenic acid being the most abundant. The ethanol extract demonstrated notable antioxidant activity, highlighting its potential for therapeutic use. Urease inhibition assays revealed a remarkable 91.35% inhibition by the extract, with an IC value of 5.6 ± 1.20 μg/mL, indicating its promising role in addressing conditions linked to urease activity. Molecular docking studies further investigated the interaction between phenolic compounds and urease, identifying hyperoside as a leading candidate, with a binding energy of -7.9 kcal/mol. Other compounds, such as rutin, luteolin, apigenin, kaempferol, hesperetin, chlorogenic acid, and rosmarinic acid, also demonstrated significant binding affinities, suggesting their potential to disrupt urease function. These findings highlight the therapeutic potential of as a source of natural bioactive compounds, offering promising avenues for the development of novel treatments for urease-related disorders and oxidative stress.

摘要

本研究考察了法氏乳杆菌(L. subsp. falezlez (Coss.) Maire)的化学成分、抗氧化特性及脲酶抑制作用。通过液相色谱-电喷雾串联质谱(LC-ESI-MS/MS)鉴定出19种不同的酚类化合物,其中绿原酸含量最为丰富。乙醇提取物表现出显著的抗氧化活性,凸显了其治疗应用潜力。脲酶抑制试验显示该提取物具有高达91.35%的显著抑制率,IC值为5.6±1.20μg/mL,表明其在解决与脲酶活性相关病症方面具有潜在作用。分子对接研究进一步探究了酚类化合物与脲酶之间的相互作用,确定金丝桃苷为主要候选物,其结合能为-7.9千卡/摩尔。其他化合物,如芦丁、木犀草素、芹菜素、山奈酚、橙皮素、绿原酸和迷迭香酸,也表现出显著的结合亲和力,表明它们具有破坏脲酶功能的潜力。这些发现突出了法氏乳杆菌作为天然生物活性化合物来源的治疗潜力,为开发脲酶相关疾病和氧化应激的新型治疗方法提供了有前景的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56c1/11719793/2fb116f7e7e9/ijms-26-00370-g001.jpg

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