Dataset Information

Nitrogen isotope fractionation in a continuous culture system containing phytoplankton and blue mussels.

ABSTRACT: An experiment was conducted to examine the fractionation of nitrogen stable isotopes in a continuous culture system containing field collected estuarine phytoplankton and blue mussels, Mytilus edulis. Nitrate and phosphate were added to culture vessels at concentrations above ambient levels and nitrogen isotope ratios (?¹⁵N) were measured in particulate matter (PM) and blue mussels over the course of the 15-day experiment. The added nutrients resulted in large productivity and chlorophyll increases in the system. Study results indicate that rapid and significant nitrogen isotope fractionation can occur during incorporation by phytoplankton grown under conditions of excess dissolved inorganic nitrogen, as shown by ?¹⁵N values depleted by as much as 9‰ in PM from the higher nutrient treatments. These lower ?¹⁵N values were also reflected in mussels exposed to culture vessels effluents. Therefore, nitrogen concentration needs to be considered when using ?¹⁵N values in biota as indicators of anthropogenic nitrogen inputs.

SUBMITTER: Pruell RJ

PROVIDER: S-EPMC7036703 | biostudies-literature | 2020 Jan

REPOSITORIES: biostudies-literature

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Nitrogen isotope fractionation in a continuous culture system containing phytoplankton and blue mussels.

Pruell Richard J RJ Taplin Bryan K BK Oczkowski Autumn J AJ Grear Jason S JS Mendoza Wilson G WG Pimenta Adam R AR Hanson Alana R AR Miller Kenneth M KM

Marine pollution bulletin 20191126

An experiment was conducted to examine the fractionation of nitrogen stable isotopes in a continuous culture system containing field collected estuarine phytoplankton and blue mussels, Mytilus edulis. Nitrate and phosphate were added to culture vessels at concentrations above ambient levels and nitrogen isotope ratios (δ<sup>15</sup>N) were measured in particulate matter (PM) and blue mussels over the course of the 15-day experiment. The added nutrients resulted in large productivity and chlorop ...[more]

PMID: 31784266

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Project description:The naturally occurring nitrogen (N) isotopes, 15N and 14N, exhibit different reaction rates during many microbial N transformation processes, which results in N isotope fractionation. Such isotope effects are critical parameters for interpreting natural stable isotope abundances as proxies for biological process rates in the environment across scales. The kinetic isotope effect of ammonia oxidation (AO) to nitrite (NO2 -), performed by ammonia-oxidizing archaea (AOA) and ammonia-oxidizing bacteria (AOB), is generally ascribed to the enzyme ammonia monooxygenase (AMO), which catalyzes the first step in this process. However, the kinetic isotope effect of AMO, or ε A M O , has been typically determined based on isotope kinetics during product formation (cumulative product, NO2 -) alone, which may have overestimated ε A M O due to possible accumulation of chemical intermediates and alternative sinks of ammonia/ammonium (NH3/NH4 +). Here, we analyzed 15N isotope fractionation during archaeal ammonia oxidation based on both isotopic changes in residual substrate (RS, NH4 +) and cumulative product (CP, NO2 -) pools in pure cultures of the soil strain Nitrososphaera viennensis EN76 and in highly enriched cultures of the marine strain Nitrosopumilus adriaticus NF5, under non-limiting substrate conditions. We obtained ε A M O values of 31.9-33.1‰ for both strains based on RS (δ15NH4 +) and showed that estimates based on CP (δ15NO2 -) give larger isotope fractionation factors by 6-8‰. Complementary analyses showed that, at the end of the growth period, microbial biomass was 15N-enriched (10.1‰), whereas nitrous oxide (N2O) was highly 15N depleted (-38.1‰) relative to the initial substrate. Although we did not determine the isotope effect of NH4 + assimilation (biomass formation) and N2O production by AOA, our results nevertheless show that the discrepancy between ε A M O estimates based on RS and CP might have derived from the incorporation of 15N-enriched residual NH4 + after AMO reaction into microbial biomass and that N2O production did not affect isotope fractionation estimates significantly.

Project description:Nitrogen is essential for microbial growth and its importance is demonstrated by the complex regulatory systems used to control the transport, assimilation and metabolism of nitrogen. Recent studies are beginning to shed light on how mycobacteria respond to nitrogen limitation and several regulators (e.g., GlnR, PII) have been characterized at a molecular level. However, despite this progress, our knowledge of the transcriptional response of mycobacteria to nitrogen limitation and its regulation is confined to batch culture.To gain further insight into the response of mycobacteria to nitrogen limitation, we developed a nitrogen-limited chemostat. We compared the transcriptional response of nitrogen-limited cells to carbon-limited cells using RNA-seq analysis in a continuous culture model at a constant growth rate.Our findings revealed significant changes in the expression of 357 genes (208 upregulated, 149 downregulated; >2-fold change, false discovery rate <5 %) in response to nitrogen limitation in continuous culture. The vast majority of the GlnR regulon (68 %) was differentially expressed under nitrogen limitation in continuous culture and approximately 52 % of the 357 genes overlapped with a previously published study investigating the response of M. smegmatis to nitrogen limitation in batch culture, while expression of only 17 % of the genes identified in batch culture were affected in our chemostat model. Moreover, we identified a unique set of 45 genes involved in the uptake and metabolism of nitrogen that were exclusive to our chemostat model. We observed strong downregulation of pathways for amino acid catabolism (i.e., alanine, aspartate, valine, proline and lysine), suggesting preservation of these amino acids for critical cellular function. We found 16 novel transcriptional regulators that were directly or indirectly involved in the global transcriptomic response of M. smegmatis to nitrogen limitation and identified several non-coding RNAs that might be involved in the transcriptional or post-transcriptional regulation of nitrogen-regulated gene expression.Using nitrogen-limited continuous culture we identified the nitrogen-responsive transcriptome of M. smegmatis, including a number of small non-coding RNAs implicated in controlling nitrogen-regulated gene expression.

Dataset Information

Nitrogen isotope fractionation in a continuous culture system containing phytoplankton and blue mussels.

Publications

Nitrogen isotope fractionation in a continuous culture system containing phytoplankton and blue mussels.

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