Jeyanthi Venkadapathi, Velusamy Palaniyandi
Department of Biotechnology, School of Bioengineering, SRM University, SRM Nagar, Kattankulathur, Chennai, 603 203 India.
Indian J Microbiol. 2016 Jun;56(2):148-57. doi: 10.1007/s12088-016-0566-8. Epub 2016 Jan 30.
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 ((1)H 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.
本研究的目的是纯化、表征并评估生物活性化合物对耐甲氧西林金黄色葡萄球菌(MRSA)的抗菌活性。抗MRSA化合物由一株名为MHB1的嗜盐细菌菌株产生。基于16S rRNA基因分析,MHB1菌株与解淀粉芽孢杆菌表现出99%的相似性。利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)分离纯生物活性化合物。薄层色谱、傅里叶变换红外光谱和质子核磁共振(¹H NMR)分析表明该化合物具有酚类性质。液相色谱-质谱(LC-MS)分析显示,纯化化合物的分子量为507 Da。该化合物抑制MRSA的生长,最低抑菌浓度(MIC)为62.5 μg mL⁻¹。将MRSA细菌暴露于该化合物的4倍MIC浓度下,使用流式细胞术分析测定细胞活力。利用扫描电子显微镜和透射电子显微镜分析确定细菌的超微结构变化。这是关于从嗜盐解淀粉芽孢杆菌MHB1中分离抗MRSA化合物的首次报道,该化合物有望成为一种生物防治剂。