Sørensen A H, Ahring B K
Institute of Environmental Science and Engineering, Technical University of Denmark, Lyngby, Denmark.
Appl Environ Microbiol. 1997 May;63(5):2001-6. doi: 10.1128/aem.63.5.2001-2006.1997.
An enzyme-linked immunosorbent assay was developed for the detection of whole cells of methanogens in samples from anaerobic continuously stirred tank digesters treating slurries of solid waste. The assay was found to allow for quantitative analysis of the most important groups of methanogens in samples from anaerobic digesters in a reproducible manner. Polyclonal antisera against eight strains of methanogens were employed in the test. The specificities of the antisera were increased by adsorption with cross-reacting cells. The reproducibility of the assay depended on the use of high-quality microtiter plates and the addition of dilute hydrochloric acid to the samples. In an experiment on different digester samples, the test demonstrated a unique pattern of different methanogenic strains present in each sample. The limited preparatory work required for the assay and the simple assay design make the test well suited for routine analysis of large numbers of samples and thus for process surveillance during operation of biogas digesters.
开发了一种酶联免疫吸附测定法,用于检测处理固体废物浆液的厌氧连续搅拌槽式消化器样品中的产甲烷菌全细胞。结果发现该测定法能够以可重复的方式对厌氧消化器样品中最重要的产甲烷菌群进行定量分析。试验中使用了针对8株产甲烷菌的多克隆抗血清。通过与交叉反应细胞吸附提高了抗血清的特异性。该测定法的可重复性取决于使用高质量的微量滴定板以及向样品中添加稀盐酸。在一项针对不同消化器样品的实验中,该试验显示出每个样品中存在的不同产甲烷菌株的独特模式。该测定法所需的准备工作有限且测定设计简单,使其非常适合对大量样品进行常规分析,从而适用于沼气消化器运行期间的过程监测。