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The link between the microbial ecology, gene expression, and biokinetics of denitrifying polyphosphate-accumulating systems under different electron acceptor combinations
- Vieira, A., Ribera-Guardia, A., Marques, R., Barreto Crespo, M. T., Oehmen, A., Carvalho, G.
- Applied microbiology and biotechnology 2018 v.102 no.15 pp. 6725-6737
- Thauera, chemical analysis, denitrification, gene expression, genetic markers, greenhouse gas emissions, greenhouse gases, high-throughput nucleotide sequencing, microbial ecology, nitrates, nitrite reductase, nitrites, nitrogen, nitrous oxide, nitrous-oxide reductase, phosphates, phosphorus, phylogeny, quantitative polymerase chain reaction, reverse transcriptase polymerase chain reaction, wastewater treatment
- The emission of the greenhouse gas nitrous oxide (N₂O) can occur during biological nutrient removal. Denitrifying enhanced biological phosphorus removal (d-EBPR) systems are an efficient means of removing phosphate and nitrogen, performed by denitrifying polyphosphate-accumulating organisms (d-PAOs). The aim of this work was to study the effect of various combinations of electron acceptors, nitrate (NO₃⁻), nitrite (NO₂⁻), and N₂O, on the denitrification pathway of a d-EBPR system. Batch tests were performed with different electron acceptor combinations, to explore the denitrification pathway. Reverse transcriptase-qPCR (RT-qPCR) and high-throughput sequencing, combined with chemical analysis, were used to study gene expression, microbial diversity, and denitrification kinetics. The potential for N₂O production was greater than the potential for its reduction in most tests. A strong correlation was observed between the N₂O reduction rate and the relative gene expression of nitrous oxide reductase per nitrite reductase (nosZ/(nirS + nirK)), suggesting that the expression of denitrifying marker genes is a strong predictor of the N₂O reduction rate. The d-EBPR community maintained a core population with low variations throughout the study. Furthermore, phylogenetic analyses of the studied marker genes revealed that the organisms actively involved in denitrification were closely related to Thauera sp., Candidatus Accumulibacter phosphatis, and Candidatus Competibacter denitrificans. Moreover, Competibacter-related OTUs seem to be important contributors to the N₂O reduction capacity of the system, likely scavenging the N₂O produced by other organisms. Overall, this study contributes to a better understanding of the microbial biochemistry and the genetics involving biological denitrification removal, important to minimize N₂O emissions in wastewater treatment plants.