Abstract

BackgroundMicrobial communities are ubiquitous in nature and play a major role in ecology, medicine, and various industrial processes. In this study, we used stoichiometric metabolic modeling to investigate a community of three species, Desulfovibrio vulgaris, Methanococcus maripaludis, and Methanosarcina barkeri, which are involved in acetogenesis and methanogenesis in anaerobic digestion for biogas production.ResultsWe first constructed and validated stoichiometric models of the core metabolism of the three species which were then assembled to community models. The community was simulated by applying the previously described concept of balanced growth demanding that all organisms of the community grow with equal specific growth rate. For predicting community compositions, we propose a novel hierarchical optimization approach: first, similar to other studies, a maximization of the specific community growth rate is performed which, however, often leads to a wide range of optimal community compositions. In a secondary optimization, we therefore also demand that all organisms must grow with maximum biomass yield (optimal substrate usage) reducing the range of predicted optimal community compositions. Simulating two-species as well as three-species communities of the three representative organisms, we gained several important insights. First, using our new optimization approach we obtained predictions on optimal community compositions for different substrates which agree well with measured data. Second, we found that the ATP maintenance coefficient influences significantly the predicted community composition, especially for small growth rates. Third, we observed that maximum methane production rates are reached under high-specific community growth rates and if at least one of the organisms converts its substrate(s) with suboptimal biomass yield. On the other hand, the maximum methane yield is obtained at low community growth rates and, again, when one of the organisms converts its substrates suboptimally and thus wastes energy. Finally, simulations in the three-species community clarify exchangeability and essentiality of the methanogens in case of alternative substrate usage and competition scenarios.ConclusionsIn summary, our study presents new methods for stoichiometric modeling of microbial communities in general and provides valuable insights in interdependencies of bacterial species involved in the biogas process.Electronic supplementary materialThe online version of this article (doi:10.1186/s13068-016-0429-x) contains supplementary material, which is available to authorized users.

Highlights

  • Microbial communities are ubiquitous in nature and play a major role in ecology, medicine, and various industrial processes

  • We investigate a two-species community consisting of D. vulgaris and M. maripaludis, and a threespecies community taking into account M. barkeri (Fig. 1)

  • Even though a plateau of maximum community growth rates for different biomass fractions exists, we argue that the single point (FDV = 0.63, FMM = 0.37) where both organisms grow with maximum biomass yield and can behave “selfish” will be the final attractor of this system

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Summary

Introduction

Microbial communities are ubiquitous in nature and play a major role in ecology, medicine, and various industrial processes. We used stoichiometric metabolic modeling to investigate a community of three species, Desulfovibrio vulgaris, Methanococcus maripaludis, and Methanosarcina barkeri, which are involved in acetogenesis and methanogenesis in anaerobic digestion for biogas production. Different strategies for modeling have been developed to investigate factors that shape microbial communities and to predict relevant interactions under different growth conditions. One of those methods is stoichiometric and constraint-based metabolic modeling that has been successfully applied for analyzing genome-scale metabolic networks of single-species [8,9,10] and was extended to the community level in recent years [11,12,13,14,15]. Stoichiometric metabolic models have been analyzed with dynamic flux balance analysis (FBA) [15, 19,20,21]

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