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一种针对不动杆菌属的rRNA靶向寡核苷酸探针的开发及其在活性污泥原位监测中的应用。

Development of an rRNA-targeted oligonucleotide probe specific for the genus Acinetobacter and its application for in situ monitoring in activated sludge.

作者信息

Wagner M, Erhart R, Manz W, Amann R, Lemmer H, Wedi D, Schleifer K H

机构信息

Lehrstuhl für Mikrobiologie, Technische Universität München, Germany.

出版信息

Appl Environ Microbiol. 1994 Mar;60(3):792-800. doi: 10.1128/aem.60.3.792-800.1994.

Abstract

Enhanced biological phosphate removal in an anaerobic-aerobic activated sludge system has generally been ascribed to members of the genus Acinetobacter. A genus-specific 16S rRNA-targeted oligonucleotide probe was developed to investigate the role of Acinetobacter spp. in situ. Nonisotopic dot blot hybridization to 66 reference strains, including the seven described Acinetobacter spp., demonstrated the expected probe specificity. Fluorescent derivatives were used for in situ monitoring of Acinetobacter spp. in the anaerobic and aerobic compartments of a sewage treatment plant with enhanced biological phosphate removal. Microbial community structures were further analyzed with oligonucleotide probes specific for the alpha, beta, or gamma subclasses of the class Proteobacteria, for the Cytophaga-Flavobacterium cluster, for gram-positive bacteria with a high G + C DNA content, and for all bacteria. Total cell counts were determined by 4',6-diamidino-2-phenylindole staining. In both the anaerobic and the aerobic basins, the activated sludge samples were dominated by members of the class Proteobacteria belonging to the beta subclass and by gram-positive bacteria with a high G + C DNA content. Acinetobacter spp. constituted less than 10% of all bacteria. For both basins, the microbial community structures determined with molecular techniques were compared with the compositions of the heterotrophic saprophytic microbiota determined with agar plating techniques. Isolates on nutrient-rich medium were classified by whole-cell hybridization with rRNA-targeted probes and fatty acid analysis.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在厌氧-好氧活性污泥系统中,强化生物除磷作用通常归因于不动杆菌属的成员。开发了一种针对16S rRNA的属特异性寡核苷酸探针,以研究不动杆菌属在原位的作用。对66株参考菌株(包括7种已描述的不动杆菌属菌种)进行非同位素斑点杂交,证明了预期的探针特异性。荧光衍生物用于对具有强化生物除磷功能的污水处理厂的厌氧和好氧区中的不动杆菌属进行原位监测。使用针对变形菌门的α、β或γ亚类、噬纤维菌-黄杆菌菌群、高G + C DNA含量的革兰氏阳性菌以及所有细菌的寡核苷酸探针,进一步分析微生物群落结构。通过4',6-二脒基-2-苯基吲哚染色确定总细胞数。在厌氧池和好氧池中,活性污泥样本均以属于β亚类的变形菌门成员和高G + C DNA含量的革兰氏阳性菌为主。不动杆菌属占所有细菌的比例不到10%。对于这两个池子,将通过分子技术确定的微生物群落结构与通过琼脂平板技术确定的异养腐生微生物群的组成进行了比较。用针对rRNA的探针和脂肪酸分析对在富含营养的培养基上分离出的菌株进行全细胞杂交分类。(摘要截短于250字)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d03f/201394/a0bf4a47144f/aem00020-0042-a.jpg

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