Journal cover Journal topic
Biogeosciences An interactive open-access journal of the European Geosciences Union
Journal topic
Volume 14, issue 2
Biogeosciences, 14, 271-283, 2017
https://doi.org/10.5194/bg-14-271-2017
© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 3.0 License.
Biogeosciences, 14, 271-283, 2017
https://doi.org/10.5194/bg-14-271-2017
© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 18 Jan 2017

Research article | 18 Jan 2017

Turnover of microbial groups and cell components in soil: 13C analysis of cellular biomarkers

Anna Gunina1,2, Michaela Dippold1, Bruno Glaser3, and Yakov Kuzyakov1,4,5 Anna Gunina et al.
  • 1Department of Agricultural Soil Science, Georg August University of Göttingen, Büsgenweg 2, 37077 Göttingen, Germany
  • 2Department of Soil Biology and Biochemistry, Dokuchaev Soil Science Institute, 119017 Moscow, Russia
  • 3Department of Soil Biogeochemistry, Institute of Agricultural and Nutritional Science, Martin Luther University Halle-Wittenberg, von-Seckendorff-Platz 3, 06120 Halle (Saale), Germany
  • 4Department of Soil Science of Temperate Ecosystems, Georg August University of Göttingen, Büsgenweg 2, 37077 Göttingen, Germany
  • 5Institute of Environmental Sciences, Kazan Federal University, 420049 Kazan, Russia

Abstract. Microorganisms regulate the carbon (C) cycle in soil, controlling the utilization and recycling of organic substances. To reveal the contribution of particular microbial groups to C utilization and turnover within the microbial cells, the fate of 13C-labelled glucose was studied under field conditions. Glucose-derived 13C was traced in cytosol, amino sugars and phospholipid fatty acid (PLFA) pools at intervals of 3, 10 and 50 days after glucose addition into the soil.

13C enrichment in PLFAs ( ∼ 1.5% of PLFA C at day 3) was an order of magnitude greater than in cytosol, showing the importance of cell membranes for initial C utilization. The 13C enrichment in amino sugars of living microorganisms at day 3 accounted for 0.57% of total C pool; as a result, we infer that the replacement of C in cell wall components is 3 times slower than that of cell membranes. The C turnover time in the cytosol (150 days) was 3 times longer than in PLFAs (47 days). Consequently, even though the cytosol pool has the fastest processing rates compared to other cellular compartments, intensive recycling of components here leads to a long C turnover time.

Both PLFA and amino-sugar profiles indicated that bacteria dominated in glucose utilization. 13C enrichment decreased with time for bacterial cell membrane components, but it remained constant or even increased for filamentous microorganisms. 13C enrichment of muramic acid was the 3.5 times greater than for galactosamine, showing a more rapid turnover of bacterial cell wall components compared to fungal. Thus, bacteria utilize a greater proportion of low-molecular-weight organic substances, whereas filamentous microorganisms are responsible for further C transformations.

Thus, tracing 13C in cellular compounds with contrasting turnover rates elucidated the role of microbial groups and their cellular compartments in C utilization and recycling in soil. The results also reflect that microbial C turnover is not restricted to the death or growth of new cells. Indeed, even within living cells, highly polymeric cell compounds are constantly replaced and renewed. This is especially important for assessing C fluxes in soil and the contribution of C from microbial residues to soil organic matter.

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