OptFill: A Tool for Infeasible Cycle-Free Gapfilling of Stoichiometric Metabolic Models

Summary: Stoichiometric metabolic modeling, particularly genome-scale models (GSMs), is now an indispensable tool for systems biology. The model reconstruction process typically involves collecting information from public databases; however, incomplete systems knowledge leaves gaps in any reconstruc...

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Main Authors: Wheaton L. Schroeder, Rajib Saha
Format: Article
Language:English
Published: Elsevier 2020-01-01
Series:iScience
Online Access:http://www.sciencedirect.com/science/article/pii/S2589004219305280
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spelling doaj-0e2e588c42ef44d1bd9e0c31fee0d31d2020-11-25T02:55:59ZengElsevieriScience2589-00422020-01-01231OptFill: A Tool for Infeasible Cycle-Free Gapfilling of Stoichiometric Metabolic ModelsWheaton L. Schroeder0Rajib Saha1Department of Chemical and Biomolecular Engineering, University of Nebraska-Lincoln, Lincoln, NE 68588, USADepartment of Chemical and Biomolecular Engineering, University of Nebraska-Lincoln, Lincoln, NE 68588, USA; Corresponding authorSummary: Stoichiometric metabolic modeling, particularly genome-scale models (GSMs), is now an indispensable tool for systems biology. The model reconstruction process typically involves collecting information from public databases; however, incomplete systems knowledge leaves gaps in any reconstruction. Current tools for addressing gaps use databases of biochemical functionalities to address gaps on a per-metabolite basis and can provide multiple solutions but cannot avoid thermodynamically infeasible cycles (TICs), invariably requiring lengthy manual curation. To address these limitations, this work introduces an optimization-based multi-step method named OptFill, which performs TIC-avoiding whole-model gapfilling. We applied OptFill to three fictional prokaryotic models of increasing sizes and to a published GSM of Escherichia coli, iJR904. This application resulted in holistic and infeasible cycle-free gapfilling solutions. In addition, OptFill can be adapted to automate inherent TICs identification in any GSM. Overall, OptFill can address critical issues in automated development of high-quality GSMs. : Metabolic Engineering; Bioinformatics; Systems Biology; Metabolic Flux Analysis Subject Areas: Metabolic Engineering, Bioinformatics, Systems Biology, Metabolic Flux Analysishttp://www.sciencedirect.com/science/article/pii/S2589004219305280
collection DOAJ
language English
format Article
sources DOAJ
author Wheaton L. Schroeder
Rajib Saha
spellingShingle Wheaton L. Schroeder
Rajib Saha
OptFill: A Tool for Infeasible Cycle-Free Gapfilling of Stoichiometric Metabolic Models
iScience
author_facet Wheaton L. Schroeder
Rajib Saha
author_sort Wheaton L. Schroeder
title OptFill: A Tool for Infeasible Cycle-Free Gapfilling of Stoichiometric Metabolic Models
title_short OptFill: A Tool for Infeasible Cycle-Free Gapfilling of Stoichiometric Metabolic Models
title_full OptFill: A Tool for Infeasible Cycle-Free Gapfilling of Stoichiometric Metabolic Models
title_fullStr OptFill: A Tool for Infeasible Cycle-Free Gapfilling of Stoichiometric Metabolic Models
title_full_unstemmed OptFill: A Tool for Infeasible Cycle-Free Gapfilling of Stoichiometric Metabolic Models
title_sort optfill: a tool for infeasible cycle-free gapfilling of stoichiometric metabolic models
publisher Elsevier
series iScience
issn 2589-0042
publishDate 2020-01-01
description Summary: Stoichiometric metabolic modeling, particularly genome-scale models (GSMs), is now an indispensable tool for systems biology. The model reconstruction process typically involves collecting information from public databases; however, incomplete systems knowledge leaves gaps in any reconstruction. Current tools for addressing gaps use databases of biochemical functionalities to address gaps on a per-metabolite basis and can provide multiple solutions but cannot avoid thermodynamically infeasible cycles (TICs), invariably requiring lengthy manual curation. To address these limitations, this work introduces an optimization-based multi-step method named OptFill, which performs TIC-avoiding whole-model gapfilling. We applied OptFill to three fictional prokaryotic models of increasing sizes and to a published GSM of Escherichia coli, iJR904. This application resulted in holistic and infeasible cycle-free gapfilling solutions. In addition, OptFill can be adapted to automate inherent TICs identification in any GSM. Overall, OptFill can address critical issues in automated development of high-quality GSMs. : Metabolic Engineering; Bioinformatics; Systems Biology; Metabolic Flux Analysis Subject Areas: Metabolic Engineering, Bioinformatics, Systems Biology, Metabolic Flux Analysis
url http://www.sciencedirect.com/science/article/pii/S2589004219305280
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