From observable fermentation data to hidden cell states: A modeling study of a mixotrophic Clostridium coculture under perfusion mode

Microbial cocultures exhibit complex population dynamics that are difficult to interpret because internal physiological states are only partially observable. In particular, active and dormant cell states can influence system-level behavior but are rarely resolved from standard fermentation measurements. In this study, we present a hybrid modeling framework that combines structured population-state reconstruction with sparse identification of nonlinear dynamics (SINDy) to analyze a Clostridium acetobutylicum - Clostridium ljungdahlii coculture under perfusion mode. The framework estimates active C a c and C l j biomass-equivalent trajectories from observable biomass and activity measurements, reconstructs dormant populations as model-constrained latent states, and uses these states to identify extracellular metabolite dynamics. After accounting for first-principles perfusion transport, SINDy identified sparse biological reaction terms associated with organic acid turnover, solvent formation, and acetone-to-isopropanol conversion. The resulting model captured active-biomass and metabolite trajectories and suggested that the coculture dynamics are consistent with acid-associated state transitions and sequential metabolic exchange. This framework provides a transparent strategy for interpreting partially observed microbial cocultures while explicitly treating dormant biomass as a latent reconstructed state.

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Journal
PLoS Computational Biology
Published
2026-09-28
DOI
https://doi.org/10.1371/journal.pcbi.1014759
Primary Topic
Microbial Metabolic Engineering and Bioproduction
Type
article
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article

From observable fermentation data to hidden cell states: A modeling study of a mixotrophic Clostridium coculture under perfusion mode

Joseph Sang‐Il Kwon, Jin Hong Mok, Hangjun Cho, Hyeongmin Seo et al.
PLoS Computational Biology
Microbial Metabolic Engineering and Bioproduction
article

From observable fermentation data to hidden cell states: A modeling study of a mixotrophic Clostridium coculture under perfusion mode

Joseph Sang‐Il Kwon, Jin Hong Mok, Hangjun Cho, Hyeongmin Seo, Juhyeon Kim
article en

Abstract

Microbial cocultures exhibit complex population dynamics that are difficult to interpret because internal physiological states are only partially observable. In particular, active and dormant cell states can influence system-level behavior but are rarely resolved from standard fermentation measurements. In this study, we present a hybrid modeling framework that combines structured population-state reconstruction with sparse identification of nonlinear dynamics (SINDy) to analyze a Clostridium acetobutylicum - Clostridium ljungdahlii coculture under perfusion mode. The framework estimates active C a c and C l j biomass-equivalent trajectories from observable biomass and activity measurements, reconstructs dormant populations as model-constrained latent states, and uses these states to identify extracellular metabolite dynamics. After accounting for first-principles perfusion transport, SINDy identified sparse biological reaction terms associated with organic acid turnover, solvent formation, and acetone-to-isopropanol conversion. The resulting model captured active-biomass and metabolite trajectories and suggested that the coculture dynamics are consistent with acid-associated state transitions and sequential metabolic exchange. This framework provides a transparent strategy for interpreting partially observed microbial cocultures while explicitly treating dormant biomass as a latent reconstructed state.

PLoS Computational BiologyVol. 22(9)
University of Iowa (US), Dongguk University (KR), Kongju National University (KR), The Ohio State University (US), Texas A&M University (US)
Openalex Percentile: Top 19%
Microbial Metabolic Engineering and Bioproduction
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From observable fermentation data to hidden cell states: A modeling study of a mixotrophic Clostridium coculture under perfusion mode — Joseph Sang‐Il Kwon, Jin Hong Mok, et al. · PLoS Computational Biology (2026) | TGRS Research Map | TGRS