Bioenergetically constrained dynamical microbial interactions govern the performance and stability of methane-producing bioreactors.

Biogas generation from organic waste by anaerobic bioreactors as renewable energy largely depends on microbial community and species interplays involved. This microbial networking is complex and time-dependent, influencing community succession and reactor performance, but remains unexplored due to the challenges in quantifying dynamics. We employed empirical dynamic modeling to analyze daily networking from a newly established bioreactor converting sucrose to biogas. Over time, microbial interactions within the three trophic (fermentative, syntrophic, and methanogenic) groups varied substantially more than between groups. Notably, versatile syntrophic bacteria like Syntrophorhabdus exhibited stronger interaction strength (0.14 ± 0.22) to hydrogen-dependent methylotrophic Methanomassiliicoccus than strictly syntrophic bacteria associated with butyrate (0.01 ± 0.01 for Syntrophomonas) and propionate (0.00 ± 0.01 for Syntrophobacter). The time-varying interaction networks were closely linked to the system performance dynamics, particularly concerning hydrogen concentrations. As community succession progressed, the stability of interaction network increased through time, accompanied by increased complexity and higher interaction strength. Causal analyses revealed intricate feedback involving catabolic energetics, community structure, and microbial interactions. These feedback mechanisms played a crucial role in regulating anaerobic degradation processes, thereby offering strategies for manipulating microbial interactions to enhance bioreactor stability and efficiency.