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首页> 外文期刊>Pharmaceutical Biology >Cell-based bioreporter assay coupled to HPLC micro-fractionation in the evaluation of antimicrobial properties of the basidiomycete fungus Pycnoporus cinnabarinus
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Cell-based bioreporter assay coupled to HPLC micro-fractionation in the evaluation of antimicrobial properties of the basidiomycete fungus Pycnoporus cinnabarinus

机译:基于细胞的生物报告者检测结合HPLC微分离技术评估担子菌真菌Pycnoporus cinnabarinus的抗菌特性

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Abstract Context Identification of bioactive components from complex natural product extracts can be a tedious process that aggravates the use of natural products in drug discovery campaigns. Objective This study presents a new approach for screening antimicrobial potential of natural product extracts by employing a bioreporter assay amenable to HPLC-based activity profiling. Materials and methods A library of 116 crude extracts was prepared from fungal culture filtrates by liquid–liquid extraction with ethyl acetate, lyophilised, and screened against Escherichia coli using TLC bioautography. Active extracts were studied further with a broth microdilution assay, which was, however, too insensitive for identifying the active microfractions after HPLC separation. Therefore, an assay based on bioluminescent E. coli K-12 (pTetLux1) strain was coupled with HPLC micro-fractionation. Results Preliminary screening yielded six fungal extracts with potential antimicrobial activity. A crude extract from a culture filtrate of the wood-rotting fungus, Pycnoporus cinnabarinus (Jacq.) P. Karst. (Polyporaceae), was selected for evaluating the functionality of the bioreporter assay in HPLC-based activity profiling. In the bioreporter assay, the IC50 value for the crude extract was 0.10?mg/mL. By integrating the bioreporter assay with HPLC micro-fractionation, the antimicrobial activity was linked to LC-UV peak of a compound in the chromatogram of the extract. This compound was isolated and identified as a fungal pigment phlebiarubrone. Discussion and conclusion HPLC-based activity profiling using the bioreporter-based approach is a valuable tool for identifying antimicrobial compound(s) from complex crude extracts, and offers improved sensitivity and speed compared with traditional antimicrobial assays, such as the turbidimetric measurement.
机译:摘要背景从复杂的天然产物提取物中鉴定生物活性成分可能是一个繁琐的过程,会加剧药物开发活动中天然产物的使用。目的本研究提出了一种新方法,该方法通过采用适合基于HPLC的活性分析的生物报告试剂分析方法来筛选天然产物提取物的抗菌潜力。材料和方法从真菌培养滤液中通过乙酸乙酯进行液-液萃取,制备了116种粗提物的文库,然后冻干,并使用薄层色谱生物自显影技术对大肠杆菌进行筛选。用肉汤微稀释测定法进一步研究了活性提取物,但是,对于HPLC分离后鉴定活性微馏分而言,它过于不灵敏。因此,将基于生物发光大肠杆菌K-12(pTetLux1)菌株的测定与HPLC微分离相结合。结果初步筛选得到了六种具有潜在抗菌活性的真菌提取物。从木腐真菌Pycnoporus cinnabarinus(Jacq。)P. Karst的培养滤液中提取的粗提物。选择了(Polyporaceae)(Polyporaceae)来评估基于HPLC的活性分析中生物报告基因测定的功能。在生物报告检测中,粗提取物的IC 50 值为0.10?mg / mL。通过将生物报告基因检测与HPLC微分离相结合,将抗菌活性与提取物色谱图中化合物的LC-UV峰关联。分离出该化合物并将其鉴定为真菌色素扑卢勃隆。讨论和结论使用基于生物报告者的方法进行的基于HPLC的活性分析是从复杂的原油提取物中鉴定抗菌化合物的有价值的工具,并且与诸如浊度法测量等传统抗菌分析方法相比,具有更高的灵敏度和速度。

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