首页> 外文期刊>亚太热带生物医学杂志(英文版) >Isolation of a small molecule with anti-MRSA activity from a mangrove symbiont Streptomyces sp. PVRK-1 and its biomedical studies inZebrafish embryos
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Isolation of a small molecule with anti-MRSA activity from a mangrove symbiont Streptomyces sp. PVRK-1 and its biomedical studies inZebrafish embryos

机译:从红树林共生链霉菌中分离出具有抗MRSA活性的小分子。 PVRK-1及其在斑马鱼胚胎中的生物医学研究

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Objective: The aim of the present study was to isolate the anti-MRSA (Methicillin ResistantStaphylococcus aureus ) molecule from the Mangrove symbiont Streptomyces and its biomedical studies in Zebrafish embryos. Methods: MRSA was isolated from the pus samples of Colachal hospitals and confirmed by amplification of mecA gene. Anti-MRSA molecule producing strain was identified by 16s rRNA gene sequencing. Anti-MRSA compound production was optimized by Solid State Fermentation (SSF) and the purification of the active molecule was carried out by TLC and RP-HPLC. The inhibitory concentration and LC50 were calculated using Statistical software SPSS. The Biomedical studies including the cardiac assay and organ toxicity assessment were carried out in Zebrafish. Results: The bioactive anti-MRSA small molecule A2 was purified by TLC with Rf value of 0.37 with 1.389 retention time at RP-HPLC. The Inhibitory Concentration of the purified molecule A2 was 30 μg/mL but, the inhibitory concentration of the MRSA in the infected embryo was 32-34 μg/mL for TLC purified molecule A2 with LC50 mean value was 61.504 μg/mL. Zebrafish toxicity was assessed in 48-60 μg/mL by observing the physiological deformities and the heart beat rates (HBR) of embryos for anti MRSA molecule showed the mean of 41.33-41.67 HBR/15 seconds for 40 μg/mL and control was 42.33-42.67 for 15 seconds which significantly showed that the anti-MRSA molecule A2 did not affected the HBR. Conclusions:Anti-MRSA molecule from Streptomyces sp PVRK-1 was isolated and biomedical studies in Zebrafish model assessed that the molecule was non toxic at the minimal inhibitory concentration of MRSA.
机译:目的:本研究的目的是从红树林共生链霉菌中分离出抗MRSA(抗甲氧西林金黄色葡萄球菌)分子,并在斑马鱼胚胎中进行生物医学研究。方法:从Colachal医院的脓液样本中分离出MRSA,并通过mecA基因扩增进行确认。通过16s rRNA基因测序鉴定产生抗MRSA分子的菌株。通过固态发酵(SSF)优化了抗MRSA化合物的生产,并通过TLC和RP-HPLC进行了活性分子的纯化。使用统计软件SPSS计算抑制浓度和LC50。在斑马鱼中进行了包括心脏测定和器官毒性评估在内的生物医学研究。结果:在RP-HPLC中,通过TLC法纯化Rf值为0.37的生物活性抗MRSA小分子A2,保留时间为1.389。纯化的分子A2的抑制浓度为30μg/ mL,但是对于TLC纯化的分子A2的LC50平均值为61.504μg/ mL,感染的胚胎中MRSA的抑制浓度为32-34μg/ mL。通过观察生理畸形,在48-60μg/ mL中评估了斑马鱼的毒性,抗MRSA分子的胚胎心跳率(HBR)显示40μg/ mL的平均值为41.33-41.67 HBR / 15秒,对照为42.33 -42.67持续15秒,这明显表明抗MRSA分子A2不影响HBR。结论:从链霉菌PVRK-1中分离了抗MRSA分子,并在斑马鱼模型中进行了生物医学研究,评估了该分子在最小抑制浓度下对MRSA无毒。

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  • 来源
    《亚太热带生物医学杂志(英文版)》 |2011年第5期|341-347|共7页
  • 作者单位

    International Centre for Nanobiotechnology ICN, Centre for Marine Science and Technology CMST, Manonmaniam Sundaranar University, Rajakkamangalam, Kanyakumari Dist-629502, TN, India;

    Xpression Biotek Pvt. Ltd, Pammam, Marthandam, Kanyakumari Dist, TN, India;

    International Centre for Nanobiotechnology ICN, Centre for Marine Science and Technology CMST, Manonmaniam Sundaranar University, Rajakkamangalam, Kanyakumari Dist-629502, TN, India;

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