Denitrification as an N2O sink

Journal Article (2019)
Author(s)

Monica Conthe (TU Delft - BT/Environmental Biotechnology)

Pawel Lycus (Norwegian University of Life Sciences (NMBU))

Magnus Arntzen (Norwegian University of Life Sciences (NMBU))

Aline Ramos da Silva (Bioclear Earth)

Åsa Frostegård (Norwegian University of Life Sciences (NMBU))

Lars R. Bakken (Norwegian University of Life Sciences (NMBU))

Robbert Kleerebezem (TU Delft - BT/Environmental Biotechnology, TU Delft - OLD BT/Cell Systems Engineering)

Mark C.M. van Loosdrecht (TU Delft - BT/Environmental Biotechnology, TU Delft - OLD BT/Cell Systems Engineering)

Research Group
BT/Environmental Biotechnology
DOI related publication
https://doi.org/10.1016/j.watres.2018.11.087
More Info
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Publication Year
2019
Language
English
Research Group
BT/Environmental Biotechnology
Volume number
151
Pages (from-to)
381-387
Reuse Rights

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Abstract

The strong greenhouse gas nitrous oxide (N2O) can be emitted from wastewater treatment systems as a byproduct of ammonium oxidation and as the last intermediate in the stepwise reduction of nitrate to N2 by denitrifying organisms. A potential strategy to reduce N2O emissions would be to enhance the activity of N2O reductase (NOS) in the denitrifying microbial community. A survey of existing literature on denitrification in wastewater treatment systems showed that the N2O reducing capacity (VmaxN2O→N2) exceeded the capacity to produce N2O (VmaxNO3→N2O) by a factor of 2–10. This suggests that denitrification can be an effective sink for N2O, potentially scavenging a fraction of the N2O produced by ammonium oxidation or abiotic reactions. We conducted a series of incubation experiments with freshly sampled activated sludge from a wastewater treatment system in Oslo and found that the ratio α = VmaxN2O→N2/VmaxNO3→N2O fluctuated between 2 and 5 in samples taken at intervals over a period of 5 weeks. Adding a cocktail of carbon substrates resulted in increasing rates, but had no significant effect on α. Based on these results – complemented with qPCR and metaproteomic data – we discuss whether the overcapacity to reduce N2O can be ascribed to gene/protein abundance ratios (nosZ/nir), or whether in-cell competition between the reductases for electrons could be of greater importance.

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