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来自一家普通污水处理厂的活性生物质的真细菌多样性。

Eubacterial diversity of activated biomass from a common effluent treatment plant.

作者信息

Kapley Atya, De Baere Thierry, Purohit Hemant J

机构信息

Environmental Genomics Unit, National Environmental Engineering Research Institute, Nehru Marg, Nagpur 440 020, India.

出版信息

Res Microbiol. 2007 Jul-Aug;158(6):494-500. doi: 10.1016/j.resmic.2007.04.004. Epub 2007 Apr 27.

Abstract

A common effluent treatment plant (CETP) is a biological wastewater treatment facility that receives wastewater from different industries. The activated biomass in the CETP survives on a wide range of chemicals with no fixed wastewater characteristics. We carried out a diversity analysis of this activated biomass using culture as well as culture-independent techniques. Using culture-based techniques, strains belonging to 26 different genera from the phyla Proteobacteria, Actinobacteria and Firmicutes were isolated. The gamma-proteobacteria was the best represented class, with 36.5% of the isolates. Bacterial diversity was also analyzed culture-independently by means of sequence determination of cloned 16S rRNA genes. Twenty-one different genera from the phyla Proteobacteria, Firmicutes, Planctomycetes and Bacteroidetes were identified. The total diversity of the activated biomass was composed of members of five known phyla, represented by 37 genera, with the Proteobacteria constituting the most abundant phylum detected. However, a very large fraction of the diversity represented a hitherto unidentified bacterial population. More than half (50.2%) of the 16S rDNA clones represented unidentified non-culturable bacteria, underlining the vast untapped diversity of CETP communities. Our results also indicate that both culture-based and culture-independent techniques should be combined to cover the microbial diversity of complex ecosystems.

摘要

通用污水处理厂(CETP)是一种接收来自不同行业废水的生物废水处理设施。CETP中的活性生物质能在多种化学物质上生存,废水特性并无固定模式。我们使用培养技术以及非培养技术对这种活性生物质进行了多样性分析。运用基于培养的技术,从变形菌门、放线菌门和厚壁菌门中分离出了属于26个不同属的菌株。γ-变形菌是占比最大的类群,占分离菌株的36.5%。还通过对克隆的16S rRNA基因进行序列测定,以非培养方式分析了细菌多样性。确定了来自变形菌门、厚壁菌门、浮霉菌门和拟杆菌门的21个不同属。活性生物质的总多样性由五个已知门的成员组成,由37个属代表,其中变形菌门是检测到的最丰富的门。然而,很大一部分多样性代表了迄今未鉴定的细菌种群。16S rDNA克隆中超过一半(50.2%)代表未鉴定的不可培养细菌,这突出了CETP群落中大量未开发的多样性。我们的结果还表明,应将基于培养的技术和非培养技术结合起来,以涵盖复杂生态系统的微生物多样性。

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