Distinguishing activity decay and cell death from bacterial decay for two types of methanogens |
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Authors: | Hao Xiaodi Cai Zhengqing Fu Kunming Zhao Dongye |
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Affiliation: | a Key Laboratory of Urban Stormwater System and Water Environment, R&D Centre for Sustainable Environmental Biotechnology, Beijing University of Civil Engineering and Architecture, Ministry of Education, Beijing 100044, PR China b Environmental Engineering Program, Department of Civil Engineering, 238 Harbert Engineering Center, Auburn University, Auburn, AL 36849, USA |
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Abstract: | As bacterial decay consists of cell death and activity decay, and the corresponding information about AOB/NOB, OHO, PAOs and GAOs has been experimentally acquired, another functional type of bacteria in biological wastewater treatment, methanogens, remains to be investigated, to gather the same information, which is extremely important for such bacteria with low growth rates. With successfully selection and enrichment of both aceticlastic and hydrogenotrophic methanogens, and by means of measuring specific methane activity (SMA) and hydrogen consumption rate (HCR), a series of decay experiments and molecular techniques such as FISH verification and LIVE/DEAD staining revealed, identified and calculated the decay and death rates of both aceticlastic and hydrogenotrophic methanogens respectively. The results indicated that the decay rates of aceticlastic and hydrogenotrophic methanogens were 0.070 and 0.034 d−1 respectively, and the death rates were thus calculated at 0.022 and 0.016 d−1 respectively. For this reason, cell deaths were only responsible for 31% and 47% of the total bacterial decay of aceticlastic and hydrogenotrophic methanogens, and activity decays actually contributed significantly to the total bacterial decay, respectively at 69% and 53%. |
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Keywords: | Methanogens Bacterial decay Cell death Activity decay Specific methanogenic activity (SMA) Hydrogen consumption rate (HCR) LIVE/DEAD staining Fluorescence in situ hybridization (FISH) |
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