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大豆植物化学物质对细菌神经氨酸酶的抑制作用及其通过 UPLC-ESI-TOF/MS 的表征。

Soybean phytochemicals responsible for bacterial neuraminidase inhibition and their characterization by UPLC-ESI-TOF/MS.

机构信息

Division of Applied Life Science (BK21 plus), IALS, Gyeongsang National University, Jinju, 52828, Republic of Korea.

Department of Pharmaceutical Engineering, IALS, Gyeongsang National University, Jinju, Republic of Korea.

出版信息

Food Funct. 2022 Jul 4;13(13):6923-6933. doi: 10.1039/d2fo00537a.

Abstract

Ethanol extract of soybean ( (L.) Merr.) showed good inhibitory activity against bacterial neuraminidase (BNA), which plays a pivotal role in the pathogenesis of a number of microbial diseases. The saponin portion fractionated through preparative HPLC (IC = 2.25 μg mL) was found to be responsible for the observed BNA inhibition. Estimation of the inhibitory effects by individual compounds showed that the soyasaponins of group B (Ba, Bb, Bb', Bc, and Bd) exhibited extremely high inhibitions (IC = 0.25-0.48 μM), whereas group A (Aa, Ab, and Ac) was almost inactive. Kinetic studies determined that group B soyasaponins were noncompetitive inhibitors. Furthermore, molecular docking experiments confirmed that soyasaponin Ba (group B) could undergo binding interactions with various residues in the binding pocket. In contrast, soyasaponin Aa (group A) failed to enter the binding pocket due to its extra scaffold structure of oligosaccharides bonded to the 22-hydroxyl position. The metabolites in the soybean extract were fully characterized using UPLC-ESI-TOF/MS.

摘要

大豆((L.)Merr.)的乙醇提取物对细菌神经氨酸酶(BNA)表现出良好的抑制活性,BNA 在许多微生物疾病的发病机制中起着关键作用。通过制备高效液相色谱法(IC = 2.25 μg mL)分离出的皂苷部分负责观察到的 BNA 抑制。对单个化合物的抑制作用进行估计表明,B 组(Ba、Bb、Bb'、Bc 和 Bd)的大豆皂素有极高的抑制作用(IC = 0.25-0.48 μM),而 A 组(Aa、Ab 和 Ac)几乎没有活性。动力学研究表明,B 组大豆皂素是一种非竞争性抑制剂。此外,分子对接实验证实,大豆皂素 Ba(B 组)可以与结合口袋中的各种残基发生结合相互作用。相比之下,由于其与 22-羟基结合的寡糖的额外支架结构,大豆皂素 Aa(A 组)无法进入结合口袋。使用 UPLC-ESI-TOF/MS 对大豆提取物中的代谢产物进行了充分的表征。

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