两种桉树属植物化合物及合成饱和烷基甘油对群体感应的抑制作用

A. Barragán, G. Silva, M. Moreno, W. Mayorga
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引用次数: 3

摘要

背景:细菌耐药性的出现促使人们寻找新的天然产物作为预防和控制微生物引起的疾病的替代起点。由于其化学结构和广泛的生物活性,在潜在的候选物中有来自八爪珊瑚属的生物活性化合物。目的:研究从两种银杏属植物中分离得到的化合物及合成的烷基甘油(AKG)的群体感应抑制(QSI)和抑菌活性。方法:采用紫色杆菌(ATCC 31532)微滴板法测定三种非极性化合物及其AKGs的QSI。从12、14、16和18个碳的烷基链上合成了四种天然存在的、饱和的、对映体纯的akg,它们都是由手性前体(R)-solketal衍生而来,并通过NMR、ESI-MS和旋光度数据对其结构进行了验证。采用圆盘扩散法测定其QSI,并在微滴板上测定其对14株临床分离细菌的最低抑菌浓度(MIC)。结果:烯二烯1、AKG合剂和AKG (2S)-3- o -十二烷基-1,2-丙二醇4对QS的抑制作用与曲酸浓度相同(分别为10µg/孔和20µg/片)。在本研究中,生物活性化合物1、硬脂油酸酯2、酰基甘油3、AKGs 4和(2S)-3- o -十四烷基-1,2-丙二醇5首次表现出体外IQS活性。此外,4和5对无毒李斯特菌和金黄色葡萄球菌(MIC值分别为32µg/mL)、粪肠球菌(MIC值分别为128µg/mL和64µg/mL)、黄体微球菌(MIC值分别为128µg/mL)和短芽孢杆菌(短芽孢杆菌)(MIC值分别为512µg/mL和64µg/mL)均表现出体外抗菌活性。结论:天然化合物1、2、3、4和5具有QSI, 4和5具有抑菌活性,是进一步研究其抑菌作用的有益选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of quorum sensing by compounds from two Eunicea species and synthetic saturated alkylglycerols
Background: the emergence of bacterial resistance has led to a search for new natural products as alternatives starting points to prevent and control diseases caused by microorganisms. Among the potential candidates were bioactive compounds from octocorals of the genus Eunicea due to their chemical structures and their wide range of biological activities. Objective: the purpose of this study was to evaluate the quorum sensing inhibition (QSI) and antibacterial activity of compounds previously isolated from two Eunicea species and synthesized alkylglycerols (AKG). Methods: the QSI of three nonpolar compounds and a mixture of AKGs from Eunicea were evaluated by a microtiter plate assay using Chromobacterium violaceum (ATCC 31532). Four naturally occurring, saturated, and enantiomerically pure AKGs, all of which were derived from the chiral precursor (R)-solketal, were synthesized from alkyl chains of 12, 14, 16 and 18 carbons, and their structures were spectroscopically verified by NMR, ESI-MS and optical rotation data. Their QSI by the disc diffusion assay and minimum inhibitory concentrations (MIC) against 14 clinical bacterial isolates in microtiter plates were determined. Results: cembradiene 1, the AKG mixture and AKG (2S)-3-O-dodecyl-1,2-propanediol 4 inhibit QS at the same concentration as kojic acid (10 µg/well or 20 µg/disc, respectively). In this study, the bioactive compounds 1, stearyl oleate 2, acylglycerol 3 and AKGs 4 and (2S)-3-O-tetradecyl-1,2-propanediol 5 showed in vitro IQS activity for the first time. Additionally, 4 and 5 displayed in vitro antibacterial activity against Listeria innocua and Staphylococcus aureus (MIC = 32 µg/mL for both 4 and 5), Enterococcus faecalis (128 µg/mL and 64 µg/mL respectively), Micrococcus luteus (128 µg/mL for both) and Brevibacillus brevis (Bacillus brevis) (512 µg/mL and 64 µg/mL respectively). Conclusion: results suggest that natural compounds 1, 2, 3, 4 and 5 showed QSI, also 4 and 5 have antibacterial activity and they are an interesting alternative to continue researching their effect against pathogenic microorganisms.
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