Abstract:dCurrently, nitritation-anammox (anaerobic ammonium oxidation) bioreactors are designed to treat wastewaters with high ammonium concentrations at mesophilic temperatures (25 to 40°C). The implementation of this technology at ambient temperatures for nitrogen removal from municipal wastewater following carbon removal may lead to more-sustainable technology with energy and cost savings. However, the application of nitritation-anammox bioreactors at low temperatures (characteristic of municipal wastewaters except… Show more
“…This indicates that the optimum temperature, for anammox biomass cultivated at 30°C, 25°C and 20°C, is equal to or higher than the maximum temperature (=30°C) tested in these experiments. A change in temperature optimum for anammox bacteria, cultivated at different temperatures, has been reported in literature for a C. Brocadia fulgida-like strain and a marine anammox strain [29,35]. Nonetheless, this observation was not confirmed in other studies [34].…”
Section: Combination Of Long-and Short-term Effect Of Temperaturementioning
The implementation of autotrophic nitrogen removal in the mainstream of a municipal wastewater treatment plant is currently pursued. Among the crucial unknown factors are the kinetic properties of anaerobic ammonium oxidising (anammox) bacteria at low temperatures. In this study we investigated the adaptation of a fast-growing anammox culture to a lower temperature. In a membrane bioreactor a highly enriched anammox community was obtained at 30°C, 25°C and 20°C. This culture was exposed to long-and short-term temperature changes. In short-term experiments the decrease in biomass-specific activity due to decrease in temperature can be described by an activation energy of 64 ± 28 kJ mol −1 . Prolonged cultivation (months) implies that cultivation at low temperatures resulted in deterioration of biomass-specific activity (Ea The reason for the deterioration of the system was related to the required long SRT in the system. The long SRT leads to an increase of non-active and non-anammox cells in the reactor, thereby decreasing the biomass-specific activity.ARTICLE HISTORY
“…This indicates that the optimum temperature, for anammox biomass cultivated at 30°C, 25°C and 20°C, is equal to or higher than the maximum temperature (=30°C) tested in these experiments. A change in temperature optimum for anammox bacteria, cultivated at different temperatures, has been reported in literature for a C. Brocadia fulgida-like strain and a marine anammox strain [29,35]. Nonetheless, this observation was not confirmed in other studies [34].…”
Section: Combination Of Long-and Short-term Effect Of Temperaturementioning
The implementation of autotrophic nitrogen removal in the mainstream of a municipal wastewater treatment plant is currently pursued. Among the crucial unknown factors are the kinetic properties of anaerobic ammonium oxidising (anammox) bacteria at low temperatures. In this study we investigated the adaptation of a fast-growing anammox culture to a lower temperature. In a membrane bioreactor a highly enriched anammox community was obtained at 30°C, 25°C and 20°C. This culture was exposed to long-and short-term temperature changes. In short-term experiments the decrease in biomass-specific activity due to decrease in temperature can be described by an activation energy of 64 ± 28 kJ mol −1 . Prolonged cultivation (months) implies that cultivation at low temperatures resulted in deterioration of biomass-specific activity (Ea The reason for the deterioration of the system was related to the required long SRT in the system. The long SRT leads to an increase of non-active and non-anammox cells in the reactor, thereby decreasing the biomass-specific activity.ARTICLE HISTORY
“…Although the measurement of the organic matter content in the influent and effluent of the SBR-Anammox system was not performed, the previous characterization of the pretreated pig slurry used to fed the CSTR-partial nitritation reactor indicated that some slowly biodegradable organic matter was present (around 100 mg C·L -1 ) which could be used for denitrification. Another reason of the lower nitrate production respect to the ammonia consumption could be attributed also to the moderate temperatures, since Hu et al [10] observed that the NO 3 -/NH 4 + ratio for the anammox bacteria in a nitritation-anammox SBR decreased from 0.18 to 0.04 when the operational temperature was decreased from 25 to 12 °C.…”
Section: Anammox Processmentioning
confidence: 99%
“…Despite the fact that the optimum performance of Anammox bacteria is obtained at 30-40 ºC [8], some studies demonstrated that it is possible the operation of Anammox systems at lower temperatures [9][10][11]. In fact this occurs naturally in the environment, since Anammox bacteria have been detected in various marine and freshwater mediums at low temperatures [12].…”
The Anammox based processes are suitable for the treatment of wastewaters characterized by a low carbon to nitrogen (C/N) ratio. The application of the Anammox process requires the availability of an effluent with a NO 2 --N/NH 4 + -N ratio composition around 1 g·g -1 , which involves the necessity of a previous step where the partial nitrification is performed. In this step the inhibition of the nitrite oxidizing bacteria (NOB) is crucial. In the present work a combined partial nitrification-Anammox two units system operated at room temperature (20 ºC) has been tested for the nitrogen removal of pre-treated pig slurry. To achieve the successful partial nitrification and inhibit the NOB activity different ammonium/inorganic carbon (NH 4 + /IC) ratios were assayed from 1.19 to 0.82 g NH 4 + -N·g -1 HCO 3 -C. This procedure provoked a decrease of the pH value to 6.0 to regulate the inhibitory effect over ammonia oxidizing bacteria (AOB) caused by free ammonia (FA). Simultaneously the NOB experienced the inhibitory effect of free nitrous acid (FNA) which avoided the presence of nitrate in the effluent. The NH 4 + /IC ratio which allowed the obtaining of the desired effluent composition (50% of both ammonium and nitrite) was of 0.82±0.02 g NH 4 + -N g -1 HCO 3 --C. The Anammox reactor was fed with the effluent of the partial nitrification unit containing a NO 2 --N/ NH 4 + -N ratio of 1 g·g -1 where a nitrogen loading rate (NLR) of 0.1 g N·L -1 ·d -1 was efficiently removed.
KeywordsAmmonium/inorganic carbon (NH 4 + /IC) ratio, Anammox, free ammonia (FA), free nitrous acid (FNA), partial nitrification.
“…If they were not completely lysed after incubation, the lysozyme-treated cells were pelleted by centrifugation for 5 min at 1,200 ϫ g. Then, the pellet was washed with 10 ml of synthetic medium (37) without substrates 3 times or until it was free of EDTA and lysozyme. The cells were resuspended in 10 ml synthetic medium containing 2 mM ammonium and nitrite, followed by anammox activity tests, as previously described (38), with modifications. In short, 10 ml cells was transferred to a 30-ml serum bottle after the pH was adjusted to 7.3.…”
bAnaerobic ammonium-oxidizing (anammox) planctomycetes oxidize ammonium in the absence of molecular oxygen with nitrite as the electron acceptor. Although planctomycetes are generally assumed to lack peptidoglycan in their cell walls, recent genome data imply that the anammox bacteria have the genes necessary to synthesize peptidoglycan-like cell wall structures. In this study, we investigated the effects of two antibacterial agents that target the integrity and synthesis of peptidoglycan (lysozyme and penicillin G) on the anammox bacterium Kuenenia stuttgartiensis. The effects of these compounds were determined in both short-term batch incubations and long-term (continuous-cultivation) growth experiments in membrane bioreactors. Lysozyme at 1 g/liter (20 mM EDTA) lysed anammox cells in less than 60 min, whereas penicillin G did not have any observable short-term effects on anammox activity. Penicillin G (0.5, 1, and 5 g/liter) reversibly inhibited the growth of anammox bacteria in continuous-culture experiments. Furthermore, transcriptome analyses of the penicillin G-treated reactor and the control reactor revealed that penicillin G treatment resulted in a 10-fold decrease in the ribosome levels of the cells. One of the cell division proteins (Kustd1438) was downregulated 25-fold. Our results suggested that anammox bacteria contain peptidoglycan-like components in their cell wall that can be targeted by lysozyme and penicillin G-sensitive proteins were involved in their synthesis. Finally, we showed that a continuous membrane reactor system with free-living planktonic cells was a very powerful tool to study the physiology of slow-growing microorganisms under physiological conditions.
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