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Experimental evaluation of decrease in the activities of polyphosphate/glycogen‐accumulating organisms due to cell death and activity decay in activated sludge
Authors:Xiaodi Hao  Qilin Wang  Yali Cao  Mark C.M. van Loosdrecht
Affiliation:1. The R&D Centre for Sustainable Environmental Biotechnology, Beijing University of Civil Engineering and Architecture, Beijing 100044, PR of China;2. telephone: 86‐10‐8060‐4512;3. fax: 86‐10‐6832‐2128;4. Department of Biotechnology, Delft University of Technology, BC Delft, the Netherlands
Abstract:Decrease in bacterial activity (biomass decay) in activated sludge can result from cell death (reduction in the amount of active bacteria) and activity decay (reduction in the specific activity of active bacteria). The goal of this study was to experimentally differentiate between cell death and activity decay as the cause of decrease in bacterial activity. By means of measuring maximal anaerobic phosphate release rates, verifying membrane integrity by live/dead staining and verifying presence of 16S rRNA with fluorescence in situ hybridization (FISH), the decay rates and death rates of polyphosphate‐accumulating organisms (PAOs) in a biological nutrient removal (BNR) system and a laboratory phosphate removing sequencing batch reactor (SBR) system were determined, respectively, under famine conditions. In addition, the decay rate and death rate of glycogen‐accumulating organisms (GAOs) in a SBR system with an enrichment culture of GAOs were also measured under famine conditions. Hereto the maximal anaerobic volatile fatty acid uptake rates, live/dead staining, and FISH were used. The experiments revealed that in the BNR and enriched PAO‐SBR systems, activity decay contributed 58% and 80% to the decreased activities of PAOs, and that cell death was responsible for 42% and 20% of decreases in their respective activities. In the enriched GAOs system, activity decay constituted a proportion of 74% of the decreased activity of GAOs, and cell death only accounted for 26% of the decrease of their activity. Biotechnol. Bioeng. 2010; 106: 399–407. © 2010 Wiley Periodicals, Inc.
Keywords:decay rate  phosphate release rate (PRR)  volatile fatty acid (VFA) uptake rate (VFAUR)  live/dead staining  fluorescence in situ hybridization (FISH)  endogenous respiration
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