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      Biases during DNA extraction of activated sludge samples revealed by high throughput sequencing

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          Abstract

          Standardization of DNA extraction is a fundamental issue of fidelity and comparability in investigations of environmental microbial communities. Commercial kits for soil or feces are often adopted for studies of activated sludge because of a lack of specific kits, but they have never been evaluated regarding their effectiveness and potential biases based on high throughput sequencing. In this study, seven common DNA extraction kits were evaluated, based on not only yield/purity but also sequencing results, using two activated sludge samples (two sub-samples each, i.e. ethanol-fixed and fresh, as-is). The results indicate that the bead-beating step is necessary for DNA extraction from activated sludge. The two kits without the bead-beating step yielded very low amounts of DNA, and the least abundant operational taxonomic units (OTUs), and significantly underestimated the Gram-positive Actinobacteria, Nitrospirae, Chloroflexi, and Alphaproteobacteria and overestimated Gammaproteobacteria, Deltaproteobacteria, Bacteroidetes, and the rare phyla whose cell walls might have been readily broken. Among the other five kits, FastDNA @ SPIN Kit for Soil extracted the most and the purest DNA. Although the number of total OTUs obtained using this kit was not the highest, the abundant OTUs and abundance of Actinobacteria demonstrated its efficiency. The three MoBio kits and one ZR kit produced fair results, but had a relatively low DNA yield and/or less Actinobacteria-related sequences. Moreover, the 50 % ethanol fixation increased the DNA yield, but did not change the sequenced microbial community in a significant way. Based on the present study, the FastDNA SPIN kit for Soil is recommended for DNA extraction of activated sludge samples. More importantly, the selection of the DNA extraction kit must be done carefully if the samples contain dominant lysing-resistant groups, such as Actinobacteria and Nitrospirae.

          Electronic supplementary material

          The online version of this article (doi:10.1007/s00253-012-4244-4) contains supplementary material, which is available to authorized users.

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          Author and article information

          Contributors
          +852-28-578551 , +852-25-595337 , zhangt@hkucc.hku.hk
          Journal
          Appl Microbiol Biotechnol
          Appl. Microbiol. Biotechnol
          Applied Microbiology and Biotechnology
          Springer-Verlag (Berlin/Heidelberg )
          0175-7598
          1432-0614
          4 July 2012
          4 July 2012
          May 2013
          : 97
          : 10
          : 4607-4616
          Affiliations
          Environmental Biotechnology Laboratory, Department of Civil Engineering, The University of Hong Kong, Pokfulam Road, Hong Kong, SAR China
          Article
          4244
          10.1007/s00253-012-4244-4
          3647099
          22760785
          c3dc54cf-31bf-4069-b10b-64f50c9e2b24
          © The Author(s) 2012
          History
          : 17 April 2012
          : 12 June 2012
          : 14 June 2012
          Categories
          Environmental Biotechnology
          Custom metadata
          © Springer-Verlag 2013

          Biotechnology
          dna extraction,bacteria,activated sludge,high throughput sequencing,commercial kit
          Biotechnology
          dna extraction, bacteria, activated sludge, high throughput sequencing, commercial kit

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