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Model selection for microbial nutrient uptake using a cost-benefit approach.

J Müller1, B A Hense2, S Marozava3

  • 1Centre for Mathematical Sciences, TU München, Boltzmannstraße 3, D-85747 Garching, Germany; Institute of Computational Biology, Helmholtz Zentrum München, D-85764 Neuherberg, Germany.

Mathematical Biosciences
|July 1, 2014
PubMed
Summary
This summary is machine-generated.

Microbial carbon source uptake is modeled using four assumptions, revealing three distinct consumption patterns: simultaneous uptake, preferred substrate repression (catabolite repression), or exclusive uptake leading to specialized subpopulations. This model quantitatively describes microbial uptake dynamics.

Keywords:
Bacterial substrate utilizationBistable nutrient uptakeCatabolite repressionHeterogeneous nutrient uptakeOptimization

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Area of Science:

  • Microbial Physiology
  • Biochemistry
  • Systems Biology

Background:

  • Microbial nutrient uptake is crucial for growth and metabolism.
  • Understanding substrate utilization dynamics is key to predicting microbial behavior.
  • Existing models often simplify the complex regulatory mechanisms of nutrient uptake.

Purpose of the Study:

  • To develop a mathematical model for microbial carbon source uptake based on fundamental assumptions.
  • To identify distinct behavioral patterns in microbial substrate utilization when presented with multiple carbon sources.
  • To validate the model's predictive capability using experimental data.

Main Methods:

  • Formulated mathematical models based on four core assumptions: saturation kinetics, cost-benefit of processing, controlled uptake, and evolutionary optimization.
  • Analyzed model predictions for two-substrate scenarios.
  • Applied batch-culture and retentostat data from Geobacter metallireducens for model validation.

Main Results:

  • Identified three distinct microbial substrate uptake patterns: simultaneous consumption, preferential consumption with repression (catabolite repression), and exclusive consumption leading to population specialization.
  • Demonstrated that the model structure can quantitatively describe uptake dynamics.
  • Showcased model applicability using experimental data for toluene, benzoate, and acetate uptake.

Conclusions:

  • The developed mathematical framework provides a robust description of microbial carbon source uptake strategies.
  • The model accurately predicts diverse substrate utilization behaviors, including catabolite repression and population specialization.
  • Experimental validation confirms the model's utility for quantitative analysis of microbial metabolism.