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首页> 外文期刊>International journal of peptide research and therapeutics >Inhibition of Methicillin Resistant Staphylococcus aureus by Bacteriocin Producing Pseudomonas aeruginosa
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Inhibition of Methicillin Resistant Staphylococcus aureus by Bacteriocin Producing Pseudomonas aeruginosa

机译:抑制甲氧西林耐药金黄色葡萄球菌,菌霉素生产假单胞菌铜绿假单胞菌

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摘要

Bacteriocins are natural antimicrobial peptides with attractive possible applications in food preservation and health care. In the present study, bacteriocin producing bacterial strain Pseudomonas aeruginosa were isolated from soil which exhibited antagonistic activity against Methicillin Resistant Staphylococcus aureus (MRSA) bacteria. The bacteriocin producing strain TA6 was confirmed as P. aeruginosa by biochemical tests and 16S rRNA gene sequence analysis. Maximum bacteriocin activity (100AUml(-1)) was observed at 37 degrees C with pH 6.0 in 24h time duration. SDS-PAGE analysis of the extracellular protein of P. aeruginosa TA6 revealed a bacteriocin-like protein with a molecular mass of similar to 10kDa. MRSA cells were treated with culture supernatant of P. aeruginosa TA6 and analyzed by FT-IR. The treated and untreated MRSA showed band variations at 671 and 3460cm(-1) corresponding to alkyl and amide group respectively. Mixed proportions of dead and live control populations were analyzed by flow cytometry to determine detection limits of the Dead/Live cells. The flow cytometry detection of defined proportions of dead (p2) and live (p1) cells at 3h were p2=60.5%; p1=39.5% and 6h p2=66.5%; p1=33.5% respectively. The scanning electron microscopy observation showed the main changes in the cell membrane structural integrity of S. aureus after exposure to the bacteriocin from P. aeruginosa TA6 at 12h incubation. Together, the results suggested that bacteriocin from P. aeruginosa TA6 was effective against MRSA.
机译:细菌素是具有有吸引力的食物保存和医疗保健的有吸引力的抗微生物肽。在本研究中,产生细菌菌株假单胞菌铜绿假单胞菌的细菌霉素与土壤抗甲氧西林金黄色葡萄球菌(MRSA)细菌的拮抗活性分离。通过生化试验和16S rRNA基因序列分析,将产生菌株Ta6的细菌素铜绿假单胞菌证实。在24小时持续时间以pH6.0在37℃下观察到最大噬菌菌素活性(100auml(-1))。 P.铜绿假单胞菌TA6细胞外蛋白的SDS-PAGE分析显示了与10kDA类似的分子量的菌丝状蛋白。用P.铜绿假单胞菌TA6的培养上清液处理MRSA细胞,并通过FT-IR分析。处理和未处理的MRSA分别显示出与烷基和酰胺基团的671和3460cm(-1)的带状变化。通过流式细胞术分析混合的死亡和活控制群体以确定死/活细胞的检测限。在3H的定义比例的定义比例的流式细胞术检测为3小时,P 2 = 60.5%; P1 = 39.5%和6小时P2 = 66.5%; P1 = 33.5%。扫描电子显微镜观察表明,在12H温育中暴露于铜绿假单胞菌TA6后,S. aureus细胞膜结构完整性的主要变化。结果表明,P.铜绿假单胞菌Ta6的细菌霉素对MRSA有效。

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