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使用荧光rRNA靶向寡核苷酸探针原位鉴定活性污泥中的诺卡氏放线菌。

In situ identification of nocardioform actinomycetes in activated sludge using fluorescent rRNA-targeted oligonucleotide probes.

作者信息

Schuppler Markus, Wagner Michael, Schön Georg, Göbel Ulf B

机构信息

Institut für Medizinische Mikrobiologie und Hygiene, Klinikum der Albert-Ludwigs-Universität Freiburg, Hermann-Herder-Straße 11, D-79104 Freiburg, Germany.

Lehrstuhl für Mikrobiologie, Technische Universität München, ArcisStraße 16, D-80290 München, Germany.

出版信息

Microbiology (Reading). 1998 Jan;144 ( Pt 1):249-259. doi: 10.1099/00221287-144-1-249.

Abstract

Hitherto, few environmental samples have been investigated by a 'full cycle rRNA analysis'. Here the results of in situ hybridization experiments with specific rRNA-targeted oligonucleotide probes developed on the basis of new sequences derived from a previously described comparative 16S rRNA analysis of nocardioform actinomycetes in activated sludge are reported. Application of the specific probes enabled identification and discrimination of the distinct populations of nocardioform actinomycetes in activated sludge. One of the specific probes (DLP) detected rod-shaped bacteria which were found in 13 of the 16 investigated sludge samples from various wastewater treatment plants, suggesting their importance in the wastewater treatment process. Another probe (GLP2) hybridized with typically branched filaments of nocardioforms mainly found in samples from enhanced biological phosphorus removal plants, suggesting that these bacteria are involved in sludge foaming. The combination of in situ hybridization with fluorescently labelled rRNA-targeted oligonucleotide probes and confocal laser scanning microscopy improved the detection of nocardioform actinomycetes, which often showed only weak signals inside the activated-sludge flocs.

摘要

迄今为止,很少有环境样本通过“全周期rRNA分析”进行研究。本文报道了基于先前描述的活性污泥中诺卡氏放线菌比较16S rRNA分析得出的新序列开发的特定rRNA靶向寡核苷酸探针的原位杂交实验结果。特异性探针的应用能够识别和区分活性污泥中不同的诺卡氏放线菌种群。其中一种特异性探针(DLP)检测到杆状细菌,在来自不同污水处理厂的16个调查污泥样本中的13个中发现了这种细菌,表明它们在废水处理过程中具有重要性。另一种探针(GLP2)与主要在强化生物除磷厂的样本中发现的典型分支丝状诺卡氏菌杂交,表明这些细菌与污泥膨胀有关。原位杂交与荧光标记的rRNA靶向寡核苷酸探针以及共聚焦激光扫描显微镜的结合改进了对诺卡氏放线菌的检测,这些细菌在活性污泥絮体内部通常仅显示微弱信号。

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