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Antioxidant activity and free radical scavenging activities of Streptomyces sp. strain MJM 10778

机译:链霉菌的抗氧化活性和清除自由基的活性。 MJM 10778菌株

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Objective:To investigate the antioxidant activity of soil-borne actinobacteria. Methods:The total phenolic contents, the level of antioxidant potential byDPPH radical scavenging activity,NO scavenging activity, andABTS radical scavenging activity in ethyl acetate extract were determined.Results:The16S rDNA sequencing analysis revealed thatStreptomyces sp. strainMJM10778, which was isolated fromHambakMountain,Korea, has99.9% similarity to Streptomyces misionensis(S. misionensis)NBRC13063.The physiological and the morphological test revealed that the strainMJM10778 has different characteristics from the strainNBRC13063. The entire antioxidant assay with the ethyl acetate extract displayed good radical scavenging activity.TheIC50 values of the strainMJM10778 extract onDPPH,NO, andABTS radicals were identified to be92.8 μg/mL,0.02 μg/mL, and134.9 μg/mL, respectively.The ethyl acetate extract of the strainMJM10778 showed an81.50% of cell viability at100 μg/mL inRaw264.7 cell viability assay.Conclusions:The results obtained suggest that the ethyl acetate extract ofStreptomyces sp. strainMJM10778 could be considered as a potential source of drug for the diseases that is caused by free radicals with its anti-oxidant activities and low cytotoxicity.
机译:目的:研究土壤传播放线菌的抗氧化活性。方法:测定乙酸乙酯提取物中总酚含量,DPPH自由基清除活性,NO清除活性和ABTS自由基清除活性的抗氧化能力。结果:16S rDNA序列分析表明链霉菌属。分离自韩国汉巴克山的MJM10778菌株与米链霉菌NBRC13063有99.9%的相似性。生理和形态学测试表明,该菌株MJM10778与NBRC13063菌株具有不同的特性。用乙酸乙酯提取物进行的整个抗氧化剂测定均显示出良好的自由基清除活性。菌株MJM10778提取物在DPPH,NO和ABTS自由基上的IC50值分别为92.8μg/ mL,0.02μg/ mL和134.9μg/ mL。在Raw264.7细胞活力试验中,菌株MJM10778的乙酸乙酯提取物在100μg/ mL下显示出81.50%的细胞活力。结论:所得结果表明链霉菌属的乙酸乙酯提取物。 MJM10778菌株可以被认为是由自由基引起的疾病的潜在药物,它具有抗氧化活性和低细胞毒性。

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  • 来源
    《亚太热带医药杂志(英文版)》 |2014年第012期|962-967|共6页
  • 作者单位

    Division of Bioscience and Bioinformatics, Myongji University, Youngin-si, Gyeonggi-do 449728, Korea;

    Center for Neutraceutical and Pharmaceutical Materials, Myongji University, Yongin-si, Gyeonggi-do 449728, Korea;

    Center for Neutraceutical and Pharmaceutical Materials, Myongji University, Yongin-si, Gyeonggi-do 449728, Korea;

    Center for Neutraceutical and Pharmaceutical Materials, Myongji University, Yongin-si, Gyeonggi-do 449728, Korea;

    Center for Neutraceutical and Pharmaceutical Materials, Myongji University, Yongin-si, Gyeonggi-do 449728, Korea;

    Center for Neutraceutical and Pharmaceutical Materials, Myongji University, Yongin-si, Gyeonggi-do 449728, Korea;

    Division of Bioscience and Bioinformatics, Myongji University, Youngin-si, Gyeonggi-do 449728, Korea;

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  • 入库时间 2022-08-19 03:58:25
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