Friedrich Udo, Prior Karola, Altendorf Karlheinz, Lipski André
Abteilung Mikrobiologie, Fachbereich Biologie/Chemie, Universität Osnabrück, 49069 Osnabrück, Germany.
Environ Microbiol. 2002 Nov;4(11):721-34. doi: 10.1046/j.1462-2920.2002.00349.x.
The bacterial diversity of an industrial biofilter used for waste gas abatement in an animal-rendering plant was investigated. A 16S rDNA clone library was generated and 444 clones were screened using computer-aided amplified ribosomal DNA restriction analysis (ARDRA). Of the screened clones, 60.8% showed unique ARDRA patterns and the remaining 174 clones were clustered into 65 groups. Almost full-length 16S rDNA sequences of 106 clones were determined and 90.5% of the clones were affiliated with the two phyla Proteobacteria and Bacteroidetes. Alpha-, Beta-, and Gammaproteobacteria accounted for 22.1, 17.6 and 18.6% respectively. Minor portions were affiliated with the Actinobacteria (2.0%), Firmicutes and Verrucomicrobia (both 1.0%), and the Deltaproteobacteria and Thermomicrobia (each 0.5%). Only six out of the 106 16S rDNA sequences exhibited similarities of more than 97% to classified bacterial species indicating that a substantial fraction of the clone sequences were derived from unknown taxa. It was also evaluated whether a database containing 281 computer-simulated bacterial rDNA fragment patterns generated from published reference sequences can be used for identification purposes. The data analysis demonstrated that this was possible only for a small number of clones, which were closely related to described bacterial strains. Rarefaction analysis of ARDRA clusters demonstrated that the 444 clones screened are insufficient to describe the entire diversity of the clone library.
对一家动物屠宰厂用于废气净化的工业生物滤池的细菌多样性进行了研究。构建了一个16S rDNA克隆文库,并使用计算机辅助的扩增核糖体DNA限制性分析(ARDRA)筛选了444个克隆。在筛选出的克隆中,60.8%显示出独特的ARDRA模式,其余174个克隆被聚类为65个组。测定了106个克隆的几乎全长16S rDNA序列,90.5%的克隆隶属于变形菌门和拟杆菌门这两个门。α-、β-和γ-变形菌分别占22.1%、17.6%和18.6%。较小部分隶属于放线菌门(2.0%)、厚壁菌门和疣微菌门(均为1.0%),以及δ-变形菌门和嗜热放线菌门(各为0.5%)。在106个16S rDNA序列中,只有6个与已分类细菌物种的相似性超过97%,这表明相当一部分克隆序列来自未知分类群。还评估了一个包含从已发表参考序列生成的281个计算机模拟细菌rDNA片段模式的数据库是否可用于鉴定目的。数据分析表明,这仅对少数与已描述细菌菌株密切相关的克隆可行。对ARDRA聚类的稀疏分析表明,筛选出的444个克隆不足以描述克隆文库的全部多样性。