Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/11844
DC FieldValueLanguage
dc.contributor.authorTsipa, Argyro-
dc.contributor.authorKoutinas, Michalis-
dc.contributor.authorUsaku, Chonlatep-
dc.contributor.authorMantalaris, Athanasios A.-
dc.date.accessioned2018-07-05T11:20:36Z-
dc.date.available2018-07-05T11:20:36Z-
dc.date.issued2018-07-
dc.identifier.citationMetabolic Engineering, 2018, vol.48, pp. 129-137en_US
dc.identifier.issn10967176-
dc.description.abstractCurrently, design and optimisation of biotechnological bioprocesses is performed either through exhaustive experimentation and/or with the use of empirical, unstructured growth kinetics models. Whereas, elaborate systems biology approaches have been recently explored, mixed-substrate utilisation is predominantly ignored despite its significance in enhancing bioprocess performance. Herein, bioprocess optimisation for an industrially-relevant bioremediation process involving a mixture of highly toxic substrates, m-xylene and toluene, was achieved through application of a novel experimental-modelling gene regulatory network – growth kinetic (GRN-GK) hybrid framework. The GRN model described the TOL and ortho-cleavage pathways in Pseudomonas putida mt-2 and captured the transcriptional kinetics expression patterns of the promoters. The GRN model informed the formulation of the growth kinetics model replacing the empirical and unstructured Monod kinetics. The GRN-GK framework's predictive capability and potential as a systematic optimal bioprocess design tool, was demonstrated by effectively predicting bioprocess performance, which was in agreement with experimental values, when compared to four commonly used models that deviated significantly from the experimental values. Significantly, a fed-batch biodegradation process was designed and optimised through the model-based control of TOL Pr promoter expression resulting in 61% and 60% enhanced pollutant removal and biomass formation, respectively, compared to the batch process. This provides strong evidence of model-based bioprocess optimisation at the gene level, rendering the GRN-GK framework as a novel and applicable approach to optimal bioprocess design. Finally, model analysis using global sensitivity analysis (GSA) suggests an alternative, systematic approach for model-driven strain modification for synthetic biology and metabolic engineering applications.en_US
dc.language.isoenen_US
dc.relation.ispartofMetabolic engineeringen_US
dc.rights© Elsevier Inc.en_US
dc.subjectBioprocess optimisationen_US
dc.subjectGene regulatory networken_US
dc.subjectMixed-substrateen_US
dc.subjectFed-batchen_US
dc.subjectMonod Kineticsen_US
dc.titleOptimal bioprocess design through a gene regulatory network – growth kinetic hybrid model: towards replacing Monod kineticsen_US
dc.typeArticleen_US
dc.collaborationImperial College Londonen_US
dc.collaborationCyprus University of Technologyen_US
dc.collaborationSilpakorn Universityen_US
dc.subject.categoryBiological Sciencesen_US
dc.journalsHybrid Open Accessen_US
dc.countryUnited Kingdomen_US
dc.countryCyprusen_US
dc.countryThailanden_US
dc.subject.fieldNatural Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1016/j.ymben.2018.04.023en_US
dc.relation.volume48en_US
cut.common.academicyear2017-2018en_US
dc.identifier.spage129en_US
dc.identifier.epage137en_US
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypearticle-
crisitem.author.deptDepartment of Chemical Engineering-
crisitem.author.facultyFaculty of Geotechnical Sciences and Environmental Management-
crisitem.author.orcid0000-0002-5371-4280-
crisitem.author.parentorgFaculty of Geotechnical Sciences and Environmental Management-
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