ArticleBMC systems biology2008
Metabolic modelling of polyhydroxyalkanoate copolymers production by mixed microbial cultures.
Article in BMC systems biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 92 citations in OpenAlex.
- Biodegradation of benzalkonium chloride: effect of carbon substrate on microbial community structure and antimicrobial susceptibility.Biodegradation · 2026Article
- Tailoring PHA copolymer types via amino acid supplementation in dairy byproduct media.Scientific reports · 2025Article
- Article
- Challenges and Perspectives of Polyhydroxyalkanoate Production From Microalgae/Cyanobacteria and Bacteria as Microbial Factories: An Assessment of Hybrid Biological System.Frontiers in bioengineering and biotechnology · 2021Review
- The Evolution of Polymer Composition during PHA Accumulation: The Significance of Reducing Equivalents.Bioengineering (Basel, Switzerland) · 2017Article
- Microbial Cometabolism and Polyhydroxyalkanoate Co-polymers.Indian journal of microbiology · 2017Review
- Metabolic Network Modeling of Microbial Interactions in Natural and Engineered Environmental Systems.Frontiers in microbiology · 2016Review
- Link between microbial composition and carbon substrate-uptake preferences in a PHA-storing community.The ISME journal · 2013Article
- OptCom: a multi-level optimization framework for the metabolic modeling and analysis of microbial communities.PLoS computational biology · 2012Article
- Microbial Consortia Engineering for Cellular Factories: in vitro to in silico systems.Computational and structural biotechnology journal · 2012Review
Corrections and comments
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Authors and funding
6 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundThis paper presents a metabolic model describing the production of polyhydroxyalkanoate (PHA) copolymers in mixed microbial cultures, using mixtures of acetic and propionic acid as carbon source material. Material and energetic balances were established on the basis of previously elucidated metabolic pathways. Equations were derived for the theoretical yields for cell growth and PHA production on mixtures of acetic and propionic acid as functions of the oxidative phosphorylation efficiency, P/O ratio. The oxidative phosphorylation efficiency was estimated from rate measurements, which in turn allowed the estimation of the theoretical yield coefficients.
resultsThe model was validated with experimental data collected in a sequencing batch reactor (SBR) operated under varying feeding conditions: feeding of acetic and propionic acid separately (control experiments), and the feeding of acetic and propionic acid simultaneously. Two different feast and famine culture enrichment strategies were studied: (i) either with acetate or (ii) with propionate as carbon source material. Metabolic flux analysis (MFA) was performed for the different feeding conditions and culture enrichment strategies. Flux balance analysis (FBA) was used to calculate optimal feeding scenarios for high quality PHA polymers production, where it was found that a suitable polymer would be obtained when acetate is fed in excess and the feeding rate of propionate is limited to approximately 0.17 C-mol/(C-mol.h). The results were compared with published pure culture metabolic studies.
conclusionAcetate was more conducive toward the enrichment of a microbial culture with higher PHA storage fluxes and yields as compared to propionate. The P/O ratio was not only influenced by the selected microbial culture, but also by the carbon substrate fed to each culture, where higher P/O ratio values were consistently observed for acetate than propionate. MFA studies suggest that when mixtures of acetate and propionate are fed to the cultures, the catabolic activity is primarily guaranteed through acetate uptake, and the characteristic P/O ratio of acetate prevails over that of propionate. This study suggests that the PHA production process by mixed microbial cultures has the potential to be comparable or even more favourable than pure cultures.
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