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首页> 外文期刊>Canadian Journal of Chemistry >Rapid screening and analysis of alcohol dehydrogenase binders from Glycyrrhiza uralensis root extract using functionalized magnetic nanoparticles coupled wilft HPLC-MS/MS
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Rapid screening and analysis of alcohol dehydrogenase binders from Glycyrrhiza uralensis root extract using functionalized magnetic nanoparticles coupled wilft HPLC-MS/MS

机译:利用功能化磁性纳米粒子耦合野生型HPLC-MS / MS快速筛选和分析甘草根提取物中的乙醇脱氢酶结合剂

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Alcohol dehydrogenase (ADH) is a key enzyme that converts ethanol into acetaldehyde. Its binders could be used to efficiently treat human toxic alcohol poisoning and suppress the acetaldehyde accumulation in alcohol hypersensitive alcoholics. In the present study, a new assay based on ADH-functionalized magnetic nanoparticles coupled with high-performance liquid chromatography - tandem mass spectrometry (HPLC-MS/MS) was developed for the rapid screening and identification of ADH binders. ADH was immobilized on silica-coated Fe3O4 magnetic nanoparticles via covalent bonds and the synthesized nanoparticles were characterized by TEM, XRD, FT-IR, and VSM. The amount of bound ADH onto magnetic nanoparticles was 80.6 μg/mg. The optimum temperature and pH for the enzymatic activity of immobilized ADH were 25 °C and 7.0, respectively. The relative activity of immobilized ADH remained 68.14% after 10 times of recycle, which exhibited good durability. Nine compounds with ADH-binding activity were screened and identified in Glycyrrhiza uralensis root extracts, among which seven compounds were first screened and identified. Experimental results proved that the proposed method could rapidly screen ADH binders from complex mixtures.
机译:酒精脱氢酶(ADH)是将乙醇转化为乙醛的关键酶。它的粘合剂可用于有效治疗人类有毒酒精中毒并抑制乙醛在酒精过敏性酒精中的积累。在本研究中,开发了一种基于ADH功能化磁性纳米颗粒与高效液相色谱-串联质谱(HPLC-MS / MS)结合的新测定法,用于快速筛选和鉴定ADH结合剂。通过共价键将ADH固定在二氧化硅包覆的Fe3O4磁性纳米颗粒上,并通过TEM,XRD,FT-IR和VSM对合成的纳米颗粒进行表征。结合到磁性纳米颗粒上的ADH的量为80.6μg/ mg。固定化ADH的酶促活性的最佳温度和pH分别为25°C和7.0。固定化ADH的相对活性在10次循环后仍保持68.14%,表现出良好的耐久性。在甘草根提取物中筛选并鉴定了9种具有ADH结合活性的化合物,其中首先筛选并鉴定了7种化合物。实验结果证明,该方法可以从复杂混合物中快速筛选出ADH结合剂。

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