The use of 16S rDNA clone libraries to describe the microbial diversity of activated sludge communities

Clone libraries were prepared from polymerase chain reaction amplified 16S rDNAs from activated sludge community DNAs. Eight different libraries from a range of samples were prepared. From each library, up to 100 clones were examined. In some libraries, the clone inserts were grouped into operational taxonomic units (OTUs) by restriction enzyme analysis (REA). Then, either the clones or representatives of OTUs were partially sequenced using either 27f or 530f conserved bacterial primers. The sequence data was phylogenettcally analysed to group the clones and the method currently gives the best insight into the activated sludge microbial community biodiversity. The method for clone library production is described and the pros and cons of the procedure are outlined. In summary, the use of clone libraries has resulted in the discovery of unimagined biodiversity in activated sludge. The abundance of some unpredicted bacterial groups (e.g. beta subclass Proteobactena) and the paucity of expected ones (e.g. Acinetobacter) highlights the inadequacy of traditional culture dependent methods that rely on sample dilution and spread plate inoculation.