Diversity of Nitrite Reductase Genes in “ Candidatus Accumulibacter phosphatis”-Dominated Cultures Enriched by Flow-Cytometric Sorting
- 15 August 2007
- journal article
- Published by American Society for Microbiology in Applied and Environmental Microbiology
- Vol. 73 (16) , 5331-5337
- https://doi.org/10.1128/aem.00175-07
Abstract
“ Candidatus Accumulibacter phosphatis” is considered a polyphosphate-accumulating organism (PAO) though it has not been isolated yet. To reveal the denitrification ability of this organism, we first concentrated this organism by flow cytometric sorting following fluorescence in situ hybridization (FISH) using specific probes for this organism. The purity of the target cells was about 97% of total cell count in the sorted sample. The PCR amplification of the nitrite reductase genes ( nirK and nirS ) from unsorted and sorted cells was performed. Although nirK and nirS were amplified from unsorted cells, only nirS was detected from sorted cells, indicating that “ Ca . Accumulibacter phosphatis” has nirS . Furthermore, nirS fragments were cloned from unsorted (Ba clone library) and sorted (Bd clone library) cells and classified by restriction fragment length polymorphism analysis. The most dominant clone in clone library Ba, which represented 62% of the total number of clones, was not found in clone library Bd. In contrast, the most dominant clone in clone library Bd, which represented 59% of the total number of clones, represented only 2% of the total number of clones in clone library Ba, indicating that this clone could be that of “ Ca . Accumulibacter phosphatis.” The sequence of this nirS clone exhibited less than 90% similarity to the sequences of known denitrifying bacteria in the database. The recovery of the nirS genes makes it likely that “ Ca . Accumulibacter phosphatis” behaves as a denitrifying PAO capable of utilizing nitrite instead of oxygen as an electron acceptor for phosphorus uptake.Keywords
This publication has 41 references indexed in Scilit:
- Metagenomic analysis of two enhanced biological phosphorus removal (EBPR) sludge communitiesNature Biotechnology, 2006
- Environmental Whole-Genome Amplification To Access Microbial Populations in Contaminated SedimentsApplied and Environmental Microbiology, 2006
- Characterization of denitrifying polyphosphate-accumulating organisms in activated sludge based on nitrite reductase geneJournal of Bioscience and Bioengineering, 2005
- Flow Sorting of Marine Bacterioplankton after Fluorescence In Situ HybridizationApplied and Environmental Microbiology, 2004
- Quantitative Assessment of Picoeukaryotes in the Natural Environment by Using Taxon-Specific Oligonucleotide Probes in Association with Tyramide Signal Amplification-Fluorescence In Situ Hybridization and Flow CytometryApplied and Environmental Microbiology, 2003
- Phosphorus and nitrogen removal with minimal COD requirement by integration of denitrifying dephosphatation and nitrification in a two-sludge systemPublished by Elsevier ,1999
- Nitrous oxide reductase (nosZ) gene-specific PCR primers for detection of denitrifiers and threenosZgenes from marine sedimentsFEMS Microbiology Letters, 1998
- Occurrence of denitrifying phosphorus removing bacteria in modified UCT-type wastewater treatment plantsWater Research, 1997
- CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choiceNucleic Acids Research, 1994
- Biological phosphorus uptake under anoxic and aerobic conditionsWater Research, 1993