Optimizing Strategies for Bio-Based Ethanol Production Using Genome-Scale Metabolic Modeling of the Hyperthermophilic Archaeon, Pyrococcus furiosus.

Archaea CO dehydrogenase Pyrococcus furiosus ethanol genome-scale modeling thermophiles

Journal

Applied and environmental microbiology
ISSN: 1098-5336
Titre abrégé: Appl Environ Microbiol
Pays: United States
ID NLM: 7605801

Informations de publication

Date de publication:
28 06 2023
Historique:
medline: 30 6 2023
pubmed: 8 6 2023
entrez: 8 6 2023
Statut: ppublish

Résumé

A genome-scale metabolic model, encompassing a total of 623 genes, 727 reactions, and 865 metabolites, was developed for Pyrococcus furiosus, an archaeon that grows optimally at 100°C by carbohydrate and peptide fermentation. The model uses subsystem-based genome annotation, along with extensive manual curation of 237 gene-reaction associations including those involved in central carbon metabolism, amino acid metabolism, and energy metabolism. The redox and energy balance of P. furiosus was investigated through random sampling of flux distributions in the model during growth on disaccharides. The core energy balance of the model was shown to depend on high acetate production and the coupling of a sodium-dependent ATP synthase and membrane-bound hydrogenase, which generates a sodium gradient in a ferredoxin-dependent manner, aligning with existing understanding of P. furiosus metabolism. The model was utilized to inform genetic engineering designs that favor the production of ethanol over acetate by implementing an NADPH and CO-dependent energy economy. The P. furiosus model is a powerful tool for understanding the relationship between generation of end products and redox/energy balance at a systems-level that will aid in the design of optimal engineering strategies for production of bio-based chemicals and fuels.

Identifiants

pubmed: 37289085
doi: 10.1128/aem.00563-23
pmc: PMC10304669
doi:

Substances chimiques

Ethanol 3K9958V90M
Acetates 0

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0056323

Subventions

Organisme : NIGMS NIH HHS
ID : T32 GM133366
Pays : United States

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Jason L Vailionis (JL)

Department of Cell and Molecular Biology, College of the Environment and Life Sciences, University of Rhode Island, Kingston, Rhode Island, USA.

Weishu Zhao (W)

Department of Cell and Molecular Biology, College of the Environment and Life Sciences, University of Rhode Island, Kingston, Rhode Island, USA.

Ke Zhang (K)

Department of Cell and Molecular Biology, College of the Environment and Life Sciences, University of Rhode Island, Kingston, Rhode Island, USA.

Dmitry A Rodionov (DA)

Sanford-Burnham-Prebys Medical Discovery Institute, La Jolla, California, USA.

Gina L Lipscomb (GL)

Department of Biochemistry and Molecular Biology, University of Georgia, Athens, Georgia, USA.

Tania N N Tanwee (TNN)

Department of Biochemistry and Molecular Biology, University of Georgia, Athens, Georgia, USA.

Hailey C O'Quinn (HC)

Department of Biochemistry and Molecular Biology, University of Georgia, Athens, Georgia, USA.

Ryan G Bing (RG)

Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina, USA.

Robert M Kelly (RM)

Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina, USA.

Michael W W Adams (MWW)

Department of Biochemistry and Molecular Biology, University of Georgia, Athens, Georgia, USA.

Ying Zhang (Y)

Department of Cell and Molecular Biology, College of the Environment and Life Sciences, University of Rhode Island, Kingston, Rhode Island, USA.

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Classifications MeSH