首页> 美国卫生研究院文献>Indian Journal of Microbiology >Anti-methicillin Resistant Staphylococcus aureus Compound Isolation from Halophilic Bacillus amyloliquefaciens MHB1 and Determination of Its Mode of Action Using Electron Microscope and Flow Cytometry Analysis
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Anti-methicillin Resistant Staphylococcus aureus Compound Isolation from Halophilic Bacillus amyloliquefaciens MHB1 and Determination of Its Mode of Action Using Electron Microscope and Flow Cytometry Analysis

机译:嗜盐解淀粉芽孢杆菌MHB1的抗甲氧西林金黄色葡萄球菌化合物分离及其作用模式的电子显微镜和流式细胞术分析

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摘要

The aim of this study was to purify, characterize and evaluate the antibacterial activity of bioactive compound against methicillin-resistant Staphylococcus aureus (MRSA). The anti-MRSA compound was produced by a halophilic bacterial strain designated as MHB1. The MHB1 strain exhibited 99 % similarity to Bacillus amyloliquefaciens based on 16S rRNA gene analysis. The culture conditions of Bacillus amyloliquefaciens MHB1 were optimized using nutritional and environmental parameters for enhanced anti-MRSA compound production. The pure bioactive compound was isolated using silica gel column chromatography and Semi-preparative High-performance liquid chromatography (Semi-preparative HPLC). The Thin layer chromatography, Fourier transform infrared spectroscopy and proton NMR (1H NMR) analysis indicated the phenolic nature of the compound. The molecular mass of the purified compound was 507 Da as revealed by Liquid chromatography-mass spectrometry (LC–MS) analysis. The compound inhibited the growth of MRSA with minimum inhibitory concentration (MIC) of 62.5 µg mL−1. MRSA bacteria exposed to 4× MIC of the compound and the cell viability was determined using flow cytometric analysis. Scanning electron microscope and Transmission electron microscope analysis was used to determine the ultrastructural changes in bacteria. This is the first report on isolation of anti-MRSA compound from halophilic B. amyloliquefaciens MHB1 and could act as a promising biocontrol agent.
机译:这项研究的目的是纯化,表征和评估生物活性化合物对耐甲氧西林的金黄色葡萄球菌(MRSA)的抗菌活性。该抗MRSA化合物由称为MHB1的嗜盐细菌菌株产生。根据16S rRNA基因分析,MHB1菌株与解淀粉芽孢杆菌具有99%的相似性。使用营养和环境参数优化解淀粉芽孢杆菌MHB1的培养条件,以提高抗MRSA化合物的产量。使用硅胶柱色谱和半制备高效液相色谱(半制备HPLC)分离纯的生物活性化合物。薄层色谱,傅立叶变换红外光谱和质子NMR( 1 H NMR)分析表明该化合物具有酚性。液相色谱-质谱(LC-MS)分析显示,纯化的化合物的分子量为507 Da。该化合物以最小抑制浓度(MIC)为62.5 µg mL -1 抑制MRSA的生长。使用流式细胞仪分析确定暴露于该化合物4 MIC的MRSA细菌和细胞活力。使用扫描电子显微镜和透射电子显微镜分析来确定细菌的超微结构变化。这是有关从嗜盐芽孢杆菌MHB1中分离抗MRSA化合物的第一份报道,它可以作为有前途的生物防治剂。

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