Dong, Liang F.; Smith, Cindy J.; Papaspyrou, Sokratis; Stott, Andrew; Osborn, A. Mark; Nedwell, David B.. 2009 Changes in Benthic Denitrification, Nitrate Ammonification, and Anammox Process Rates and Nitrate and Nitrite Reductase Gene Abundances along an Estuarine Nutrient Gradient (the Colne Estuary, United Kingdom). Applied and Environmental Microbiology, 75. 3171-3179. 10.1128/AEM.02511-08
Abstract
Estuarine sediments are the location for significant bacterial removal of anthropogenically derived inorganic
nitrogen, in particular nitrate, from the aquatic environment. In this study, rates of benthic denitrification
(DN), dissimilatory nitrate reduction to ammonium (DNRA), and anammox (AN) at three sites along a nitrate
concentration gradient in the Colne estuary, United Kingdom, were determined, and the numbers of functional
genes (narG, napA, nirS, and nrfA) and corresponding transcripts encoding enzymes mediating nitrate reduction
were determined by reverse transcription-quantitative PCR. In situ rates of DN and DNRA decreased
toward the estuary mouth, with the findings from slurry experiments suggesting that the potential for DNRA
increased while the DN potential decreased as nitrate concentrations declined. AN was detected only at the
estuary head, accounting for ca 30% of N2 formation, with 16S rRNA genes from anammox-related bacteria also
detected only at this site. Numbers of narG genes declined along the estuary, while napA gene numbers were
stable, suggesting that NAP-mediated nitrate reduction remained important at low nitrate concentrations. nirS
gene numbers (as indicators of DN) also decreased along the estuary, whereas nrfA (an indicator for DNRA)
was detected only at the two uppermost sites. Similarly, nitrate and nitrite reductase gene transcripts were
detected only at the top two sites. A regression analysis of log(n plus 1) process rate data and log(n plus 1) mean
gene abundances showed significant relationships between DN and nirS and between DNRA and nrfA. Although
these log-log relationships indicate an underlying relationship between the genetic potential for nitrate
reduction and the corresponding process activity, fine-scale environmentally induced changes in rates of
nitrate reduction are likely to be controlled at cellular and protein levels.
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