4.7 Article

Biochemical modeling of microbial memory effects and catabolite repression on soil organic carbon compounds

Journal

SOIL BIOLOGY & BIOCHEMISTRY
Volume 128, Issue -, Pages 1-12

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.soilbio.2018.10.003

Keywords

Diawdc growth; Catabolite repression; Substrate preferential consumption; Michaelis-menten-monod; Carbon; Soil organic matter

Categories

Funding

  1. Sydney Research Excellence Initiative (SREI 2020) of The University of Sydney
  2. Mid Career Research Award of The University of Sydney
  3. Sydney Research Accelerator Fellowship (SOAR) by The University of Sydney
  4. Office of Science, Office of Biological and Environmental Research of the U.S. Department of Energy [DE-AC02-05CH11231]

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Microbial decomposition of Soil Organic Matter (SOM) is largely controlled by environmental and edaphic factors such as temperature, pH, and moisture. However, microbial metabolism is controlled by catabolite repression, which leads microbes to grow on preferred nutrient and energy sources first. In particular, Catabolite Repression for Carbon (CR-C) defines the hierarchical preference of bacteria for particular C sources. This control depends on the presence of signal molecules conferring bacteria a memory for recent growth conditions on less preferred C sources. The combined effect of catabolite repression and microbial memory (called here Memory Associated Catabolite Repression for Carbon, MACR-C) has not yet been investigated in detail. First, we use observations and a numerical model to test the hypothesis that MACR-C explains substrate preferential consumption in a simple, 2-C substrate system, whereas Michaelis-Menten-Monod kinetics of competitive substrate consumption, non-competitive inhibition, or their combination, do not. Next, we carry out numerical analyses to explore the sensitivity of (1) estimated parameters to experimental observations and (2) model structure to steady-state substrate concentration under pulse or continuous substrate application. Our results show that MACR-C substantially affected substrate consumption and microbial readiness to switch between C sources.

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