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潜在脂肪酸作为抗口腔细菌的抗菌剂:来自罗勒(奥勒冈)的变异链球菌和血链球菌的体外和计算机模拟研究。

Potential Fatty Acid as Antibacterial Agent Against Oral Bacteria of Streptococcus mutans and Streptococcus sanguinis from Basil (Ocimum americanum): In vitro and In silico Studies.

机构信息

Department of Pediatric Dentistry, Faculty of Dentistry, Universitas Padjadjaran - Bandung, Indonesia.

Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Padjadjaran, Sumedang, Indonesia.

出版信息

Curr Drug Discov Technol. 2021;18(4):532-541. doi: 10.2174/1570163817666200712171652.

DOI:10.2174/1570163817666200712171652
PMID:32652913
Abstract

BACKGROUND

Streptococcus mutans and Streptococcus sanguinis are Gram-positive bacteria that cause dental caries. MurA enzyme acts as a catalyst in the formation of peptidoglycan in bacterial cell walls, making it ideal as an antibacterial target. Basil (Ocimum americanum) is an edible plant that is diverse and has been used as a herbal medicine for a long time. It has been reported that basil has a pharmacological effect as well as antibacterial activity. The purpose of this study was to identify antibacterial compounds in O. americanum and analyze their inhibition activity on MurA enzyme.

METHODS

Fresh leaves from O. americanum were extracted with n-hexane and purified by a combination of column chromatography on normal and reverse phases together with in vitro bioactivity assay against S. mutans ATCC 25175 and S. sanguinis ATCC 10556, respectively, while in silico molecular docking simulation of lauric acid (1) was conducted using PyRx 0.8.

RESULTS

The structure determination of antibacterial compound by spectroscopic methods resulted in an active compound lauric acid (1). The in vitro evaluation of antibacterial activity in compound 1 showed Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) values of 78.13 and 156.3 ppm and 1250 and 2500 ppm against S. sanguinis and S. mutans, respectively. Further analysis and in silico evaluation determined lauric acid (1) as MurA Enzyme inhibitor. Lauric acid (1) showed a binding affinity of -5.2 Kcal/mol, which was higher than fosfomycin.

CONCLUSION

Lauric acid showed the potential as a new natural antibacterial agent through MurA inhibition in bacterial cell wall biosynthesis.

摘要

背景

变形链球菌和血链球菌是引起龋齿的革兰氏阳性菌。MurA 酶在细菌细胞壁中肽聚糖的形成中起催化作用,使其成为理想的抗菌靶点。罗勒(Ocimum americanum)是一种可食用的植物,种类繁多,长期以来一直被用作草药。据报道,罗勒具有药理作用和抗菌活性。本研究旨在鉴定罗勒中的抗菌化合物,并分析其对 MurA 酶的抑制活性。

方法

用正己烷提取新鲜的罗勒叶,通过正相和反相柱层析的组合进行纯化,并分别对 S. mutans ATCC 25175 和 S. sanguinis ATCC 10556 进行体外生物活性测定,同时使用 PyRx 0.8 对月桂酸(1)进行计算机模拟分子对接。

结果

通过光谱方法确定了抗菌化合物的结构,得到了活性化合物月桂酸(1)。化合物 1 的体外抗菌活性评价显示,对 S. sanguinis 和 S. mutans 的最小抑菌浓度(MIC)和最小杀菌浓度(MBC)值分别为 78.13 和 156.3 ppm 以及 1250 和 2500 ppm。进一步的分析和计算机模拟评估确定月桂酸(1)为 MurA 酶抑制剂。月桂酸(1)的结合亲和力为-5.2 Kcal/mol,高于磷霉素。

结论

月桂酸通过抑制细菌细胞壁生物合成中的 MurA,显示出作为新型天然抗菌剂的潜力。

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