4.7 Article

15N-amino sugar stable isotope probing (15N-SIP) to trace the assimilation of fertiliser-N by soil bacterial and fungal communities

Journal

SOIL BIOLOGY & BIOCHEMISTRY
Volume 138, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.soilbio.2019.107599

Keywords

N-15-stable isotope probing; Microbial immobilization; Nitrogen uptake; Nutrient cycling; Organic matter cycling

Categories

Funding

  1. Wessex Water [NE/J017523/1]
  2. NERC [R8/H10/63, NE/K010689/1]
  3. UK Biotechnology and Biological Sciences Research Council (BBSRC)
  4. BBSRC [BB/P004539/1] Funding Source: UKRI

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Although amino sugars represent a major component of soil organic nitrogen (ON), the assimilation of nitrate (NO3-) and ammonium (NH4+) into amino sugars (AS) by soil bacteria and fungi represents a neglected aspect of the global N cycle. A deeper knowledge of AS responses to N fertiliser addition may help enhance N use efficiency (NUE) within agricultural systems. Our aim was to extend a sensitive compound-specific N-15-stable isotope probing (SIP) approach developed for amino acids (AAs) to investigate the immobilization of inorganic N into a range of amino sugars (muramic acid, glucosamine, galactosamine, mannosamine). Laboratory incubations using N-15-ammonium and N-15-nitrate applied at agriculturally relevant rates (190 and 100 kg N ha(-1) for (NH4+)-N-15 and (NO3-)-N-15, respectively) were carried out to obtain quantitative measures of N-assimilation into the AS pool of a grassland soil over a 32-d period. Using gas chromatography-combustion-isotope ratio mass spectrometry (GC-C-IRMS) we found that delta N-15 values for individual AS reflected differences in routing of the applied ammonium and nitrate. The contrasting N-assimilation dynamics of bacterial and fungal communities were demonstrated through determinations of percentage N-15 incorporation into diagnostic AS. N-assimilation dynamics of the bacterial community were altered with the applied substrate whilst fungal N-assimilation dynamics were unaffected. Rates and fluxes of the applied N-substrates into the bacterial AS pool reflected known biosynthetic pathways for AS, with fungal glucosamine appearing to be biosynthetically further from the applied substrates than bacterial glucosamine due to different turnover rates. This sensitive and specific compound-specific N-15-SIP approach using AS, building on existing approaches with AAs, enables differentiation of N-assimilation dynamics within the microbial community and assessment of microbial NUE with agriculturally relevant fertilisation rates.

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