首页> 外文期刊>International Journal of Pharmacy and Pharmaceutical Sciences >STUDY ON ANTIMICROBIAL ACTIVITY OF NOCARDIA sp. STRAIN TP1 ISOLATED FROM TANGKUBAN PERAHU SOIL, WEST JAVA, INDONESIA
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STUDY ON ANTIMICROBIAL ACTIVITY OF NOCARDIA sp. STRAIN TP1 ISOLATED FROM TANGKUBAN PERAHU SOIL, WEST JAVA, INDONESIA

机译:诺卡氏菌的抑菌活性研究。源自印度尼西亚西爪哇唐库班佩拉胡土壤的TP1菌株

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Objective: The aim of this research was to investigate the growth profile of Nocardia sp. strain TP1, as well as antimicrobial acitvity of Nocardia sp. strain TP1 fermentation broth and extract. Methods: Antimicrobial compound was produced by liquid fermentation method. Microbe used in this study was identified as Nocardia sp. strain TP1. Nocardia sp. strain TP1 was isolated from soil of Tangkuban Perahu volc ano region, West Java Indonesia. This isolate was grown in several media composition composed of glucose, starch, tryptone, yeast extract, and calcium carbonate using 7 L fermentor. The fermentation broth was extracted by liquid-liquid extraction using n-butanol, ethyl acetate and chloroform solvents at pH 4.5, 7 and 9. Then, the active substance was detected by bioautography using ethyl acetate-toluene (8:2) as eluent. Results: The highest activity of the culture against methicillin sensitive Staphylococcus aureus (MSSA) was shown after 36 and 38 hours fermentation and 36 hours after fermentation against M. gypseum. Antimicrobial activity of n-butanol extract at pH 7 was shown by MIC value of 128 ppm and 64 ppm against MSSA and M. gypseum, respectively. Bioautography examination on MSSA and M. gypseum showed antimicrobial activity was produced by active spot which gave Rf value of 0.85. Conclusion: Secondary metabolite was produced by Nocardia sp. strain TP1 in fermentation broth active against MSSA and M. gypseum
机译:目的:本研究的目的是调查诺卡氏菌的生长概况。菌株TP1以及诺卡氏菌(Nocardia sp。)的抗菌活性。菌株TP1发酵液和提取物。方法:采用液体发酵法生产抗菌化合物。在这项研究中使用的微生物被鉴定为诺卡氏菌。菌株TP1。诺卡氏菌菌株TP1是从印度尼西亚西爪哇省的Tangkuban Perahu volc ano地区的土壤中分离出来的。该分离株使用7 L发酵罐在几种葡萄糖,淀粉,胰蛋白try,酵母提取物和碳酸钙组成的培养基中生长。通过使用正丁醇,乙酸乙酯和氯仿溶剂在pH 4.5、7和9下进行液-液萃取来提取发酵液。然后,使用乙酸乙酯-甲苯(8:2)作为洗脱液通过生物自显影法检测活性物质。结果:发酵后36和38小时以及发酵后36小时,培养物对甲氧西林敏感的金黄色葡萄球菌(MSSA)具有最高活性。正丁醇提取物在pH 7下的抗微生物活性分别通过MIC值对MSSA和石膏霉菌的MIC值为128 ppm和64 ppm来显示。对MSSA和石膏支原体进行生物自显影检查表明,活性点产生了抗菌活性,Rf值为0.85。结论:二次代谢产物是诺卡氏菌产生的。对MSSA和石膏霉菌有活性的发酵液中的TP1菌株;

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