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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Antibacterial and Antibiotic Modifying Potential of Crude Extracts, Fractions, and Compounds from Acacia polyacantha Willd. against MDR Gram-Negative Bacteria
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Antibacterial and Antibiotic Modifying Potential of Crude Extracts, Fractions, and Compounds from Acacia polyacantha Willd. against MDR Gram-Negative Bacteria

机译:粗提取物,馏分和来自金合欢聚乙作用的抗生素和抗生素修饰潜力。 对抗MDR革兰氏阴性细菌

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The present study aimed to assess the in vitro antibacterial and antibiotic modifying activities of methanol extracts prepared from the leaf (APL) and bark (APB) of Acacia polyacantha, fractions (APLa-d) and compounds isolated from APL against a panel of multidrug resistant (MDR) Gram-negative bacteria. Leaf extract was subjected to column chromatography for compounds isolation; antibacterial assays were performed on samples alone and with an efflux pump inhibitor (EPI), respectively, and several antibiotics on the tested bacteria. The phytochemical investigation of APL led to the isolation of stigmasterol (1), beta-amyrin (2), 3-O-beta-D-glucopyranosylstigmasterol (3), 3-O-methyl-D-chiro-inositol (4), epicatechin (5), quercetin-3-O-glucoside (6), 3-0-[beta-D-xylopyranosyl-(1->4)-bet-D-galactopyranosyl]-oleanolic acid (7), and 3-O-[beta-galactopyranosyl-(1->4)-beta-D-galactopyranosyl]' oleanolic acid (8). APL and APB had minimal inhibitory concentration (MIC) values < -= 1024 mug/mL on 73.3% and 46.7% of the tested bacteria, respectively. APLb and APLd were effective against 88.9% of tested bacterial species with compound 8 showing the highest activity inhibiting 88.9% of tested bacteria. The EPI, phenylalanine-arginine-beta-naphthylamide (PAbetaN), strongly improved the activity of APL, APLb, APLd, and compound 8 on all tested bacteria. Synergistic effects were obtained when APL and compounds 7 and 8 were combined with erythromycin (ERY), gentamycin (GEN), ciprofloxacin (CIP), and norfloxacin (NOR). The present study demonstrates the antibacterial potential of Acacia polyacantha and its constituents to combat bacterial infections alone or in combination with EPI.
机译:本研究旨在评估由叶片(APL)和树皮(APLA-D)和从Apl分离的抗APL与多药物抗体面板分离的叶片(APL)和树皮(APB)制备的甲醇提取物的体外抗菌和抗生素修饰活性(MDR)革兰氏阴性细菌。对叶子提取物进行柱色谱,用于化合物分离;对单独的样品进行抗菌测定,分别对渗透泵抑制剂(EPI)进行,并且在测试的细菌上进行几种抗生素。 APL的植物化学研究导致Stigmasterol(1),β-氨酰胺(2),3-O-β-D-吡喃葡萄糖囊糖基甾醇(3),3-O-甲基-D-甲基肌醇(4)的分离, EPICATECHIN(5),槲皮素-3-O-葡糖苷(6),3-0- [β-D-甲基吡喃糖基 - (1-> 4)-β-D-半乳糖基] - oliEnolic acid酸(7)和3- O- [β-半乳糖酰基 - (1-> 4)-β-D-半乳糖醇]'OleAlic acid(8)。 APL和APB分别具有最小的抑制浓度(MIC)值,分别对测试细菌的73.3%和46.7%的73.3%和46.7%的抑制浓度(MIC)值。 APLB和APLD对88.9%的测试细菌物种有效,化合物8显示出抑制88.9%的测试细菌的最高活性。 EPI,苯丙氨酸 - 精氨酸 - β-萘氨基(pabetan),强烈改善了所有测试细菌的APL,APLB,APLD和化合物8的活性。当APL和化合物7和8与红霉素(ery),庆大霉素(Gen),环丙沙星(CIP)和NORFLOXACIN(NOR)组合时获得协同效应。本研究证明了金合欢聚乙酰胺的抗菌潜力及其组分,以单独或与EPI组合进行对抗细菌感染。

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