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dc.contributor.authorSchulze, Markus
dc.contributor.authorNiemann, Julia
dc.contributor.authorWijffels, Rene Hubertus
dc.contributor.authorMatuszczyk, Jens
dc.contributor.authorMartens, Dirk E.
dc.date.accessioned2022-07-12T20:00:57Z
dc.date.available2022-07-12T20:00:57Z
dc.date.created2021-10-11T10:46:47Z
dc.date.issued2021
dc.identifier.citationSchulze, M., Niemann, J., Wijffels, R. H., Matuszczyk, J. & Martens, D. E. (2021). Rapid intensification of an established CHO cell fed-batch process. Biotechnology Progress, 38(1): e3213. doi:en_US
dc.identifier.issn1520-6033
dc.identifier.urihttps://hdl.handle.net/11250/3004951
dc.description.abstractCurrently, the mammalian biomanufacturing industry explores process intensification (PI) to meet upcoming demands of biotherapeutics while keeping production flexible but, more importantly, as economic as possible. However, intensified processes often require more development time compared with conventional fed-batches (FBs) preventing their implementation. Hence, rapid and efficient, yet straightforward strategies for PI are needed. In this study we demonstrate such a strategy for the intensification of an N-stage FB by implementing N-1 perfusion cell culture and high inoculum cell densities resulting in a robust intensified FB (iFB). Furthermore, we show successful combination of such an iFB with the addition of productivity enhancers, which has not been reported so far. The conventional CHO cell FB process was step-wise improved and intensified rapidly in multi-parallel small-scale bioreactors using N-1 perfusion. The iFBs were performed in 15 and 250 ml bioreactors and allowed to evaluate the impact on key process indicators (KPI): the space–time yield (STY) was successfully doubled from 0.28 to 0.55 g/L d, while product quality was maintained. This gain was generated by initially increasing the inoculation density, thus shrinking process time, and second supplementation with butyric acid (BA), which reduced cell growth and enhanced cell-specific productivity from ~25 to 37 pg/(cell d). Potential impacts of PI on cell metabolism were evaluated using flux balance analysis. Initial metabolic differences between the standard and intensified process were observed but disappeared quickly. This shows that PI can be achieved rapidly for new as well as existing processes without introducing sustained changes in cellular and metabolic behavior.en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleRapid intensification of an established CHO cell fed-batch processen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2021 The Authorsen_US
dc.subject.nsiVDP::Matematikk og Naturvitenskap: 400::Basale biofag: 470::Molekylærbiologi: 473en_US
dc.subject.nsiVDP::Teknologi: 500::Medisinsk teknologi: 620en_US
dc.subject.nsiVDP::Teknologi: 500::Bioteknologi: 590en_US
dc.source.pagenumber15en_US
dc.source.volume38en_US
dc.source.journalBiotechnology progressen_US
dc.source.issue1en_US
dc.identifier.doi10.1002/btpr.3213
dc.identifier.cristin1944806
dc.source.articlenumbere3213en_US


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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