首页> 外文期刊>Cytometry: The Journal of the Society for Analytical Cytology >QUANTITATIVE FLOW CYTOMETRIC DETECTION OF SPECIFIC MICROORGANISMS IN SOIL SAMPLES USING RRNA TARGETED FLUORESCENT PROBES AND ETHIDIUM BROMIDE
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QUANTITATIVE FLOW CYTOMETRIC DETECTION OF SPECIFIC MICROORGANISMS IN SOIL SAMPLES USING RRNA TARGETED FLUORESCENT PROBES AND ETHIDIUM BROMIDE

机译:RRNA靶向荧光探针和溴化乙锭定量检测生物样品中特定微生物的流式细胞仪

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Specific detection and accurate enumeration of microorganisms in the environment have been hampered by the lack of suitable techniques, A three-parameter flow cytometric method (FCM) was developed to detect quantitatively Sphingomonas sp, strain 107 inoculated into soil samples, By combining light scattering profiles (i.e., morphological properties), ethidium bromide (EtBr) influx (i.e., wall permeability), and fluorescence in situ hybridization against the 16S rRNA (i.e., detection specificity), we could accurately discriminate the bacterium of interest from the indigenous microflora and soil debris, EtBr was used, first, to determine the optimal cell wall permeabilization treatment to allow oligonucleotide probes to enter the bacterial cells and, second, to achieve clear discrimination of fixed cells from debris in soil samples. This method allowed effective qualitative and quantitative analysis by fluorescence in situ hybridization. The results showed that the detection threshold by FCM was 3 x 10(4) cells/g of dry soil. Cell counts deduced from FCM analysis mere similar to those obtained by the colony forming unit assay when soils contained fewer than 3 x 10(6) cells/g dry soil, This method should be useful for either quantitative monitoring of microorganisms inoculated in contaminated soil samples during bioremediation or detecting known bacterial strains in environmental samples. (C) Wiley-Liss, Inc. [References: 28]
机译:由于缺乏合适的技术,环境中微生物的特异性检测和精确计数受到阻碍,开发了一种三参数流式细胞术(FCM),通过结合光散射图谱定量检测接种到土壤样品中的鞘氨醇单胞菌sp。107菌株(即形态特征),溴化乙锭(EtBr)流入(即壁渗透性)和针对16S rRNA的荧光原位杂交(即检测特异性),我们可以准确地将目标细菌与本地微生物区系和土壤区分开来碎片,首先使用EtBr来确定最佳的细胞壁通透性处理,以允许寡核苷酸探针进入细菌细胞,其次,从土壤样品中的碎片中清晰区分固定细胞。这种方法可以通过荧光原位杂交进行有效的定性和定量分析。结果表明,FCM的检测阈值为3 x 10(4)细胞/ g干燥土壤。从FCM分析得出的细胞数仅类似于土壤每克干燥土壤中少于3 x 10(6)个细胞/克时通过菌落形成单位测定获得的细胞数,该方法对于定量监测污染土壤样品中接种的微生物均应有用生物修复或检测环境样品中已知细菌菌株的过程中。 (C)Wiley-Liss,Inc. [参考:28]

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