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Nitrogen and oxygen isotope fractionation during dissimilatory nitrate reduction by denitrifying bacteria
Journal
Limnology and Oceanography
Volume
53
Number
6
Pages / Article-Number
2533-2545
Abstract
We report the first measurements of coupled nitrogen (N) and oxygen (O) isotope fractionation of nitrate by laboratory cultures of denitrifying bacteria. Two seawater strains (Pseudomonas stutzeri, Ochrobactrum sp.) and three freshwater strains (Paracoccus denitrificans, Pseudomonas chlororaphis, Rhodobacter sphaeroides) were examined. Among four strains of facultative anaerobic denitrifiers, N and O isotope effects were variable, ranging from 5 parts per thousand to 25 parts per thousand, with evidence for a drop in the isotope effects as nitrate concentrations approached the half-saturation constant for nitrate transport. O isotope effects were similar to their corresponding N isotope effect, such that the progressive increase in nitrate delta O-18, when plotted against that in delta N-15 (where delta O-18(sample) = [(O-18 : O-16) sample/(O-18 : O-16)(reference) - 1] x 1000, and delta N-15(sample) = [(N-15 : N-14)(sample)/(N-15 : N-14)(reference) - 1] x 1000), yielded slopes of 0.86 to 1.02, with a mean value of 0.96. R. sphaeroides, a photo-heterotroph that possesses only a periplasmic (nonrespiring) dissimilatory nitrate reductase, showed less variability in nitrate N isotope effects, between 13 parts per thousand and 20 parts per thousand, with a modal value of similar to 15 parts per thousand. In contrast to the respiratory denitrifiers, R. sphaeroides consistently showed a distinct ratio of delta O-18 to delta N-15 change of similar to 0.62. We hypothesize that heavy N and O isotope discrimination during respiratory denitrification occurs during the intracellular reduction of nitrate by the respiratory nitrate reductase, and the observed magnitude of fractionation is likely regulated by the ratio of cellular nitrate efflux relative to uptake. The data for R. sphaeroides are consistent with isotope discrimination directly reflecting the N and O isotope effects of the periplasmic nitrate reductase NAP, without modification by nitrate uptake and efflux.
