dc.contributorUniversidade Federal de São Carlos (UFSCar)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:24:03Z
dc.date.available2014-05-20T15:24:03Z
dc.date.created2014-05-20T15:24:03Z
dc.date.issued2001-01-01
dc.identifierChemical Engineering Science. Oxford: Pergamon-Elsevier B.V., v. 56, n. 2, p. 419-425, 2001.
dc.identifier0009-2509
dc.identifierhttp://hdl.handle.net/11449/34710
dc.identifier10.1016/S0009-2509(00)00244-X
dc.identifierWOS:000167291200018
dc.description.abstractViable cells immobilized in inert supports are currently studied for a wide range of bioprocesses. The intrinsic advantages of such systems over suspended cultures incite new research, including studies on fundamental aspects as well as on the industrial viability of these non-conventional processes. In aerobic culture of filamentous fungi, scale-up is hindered by oxygen mass transfer limitation through the support material and bioprocess kinetics must be studied together with mass transfer limitation. In this work, experimental and simulated data of cephalosporin C production were compared. Concentrations in the bulk fermentation medium and cellular mass profiles inside the bioparticles are focused. Immobilized cells were used in a tower bioreactor, operated in fed-batch mode. To describe the radial variation of oxygen concentration within the pellet, a dead core model was used. Despite the extremely low sugar concentrations, bioreaction rates in the pellets were limited by the dissolved oxygen concentration. Cell growth occurs only in the outer layers, a result also confirmed by scanning electron microscopy. (C) 2001 Elsevier B.V. Ltd. All rights reserved.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationChemical Engineering Science
dc.relation3.306
dc.relation1,043
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectcephalosporin C
dc.subjectbeta-lactam
dc.subjectCephalosporium acremonium
dc.subjectdead core model
dc.subjectfed-batch
dc.titleThe dead core model applied to beads with immobilized cells in a fed-batch cephalosporin C production bioprocess
dc.typeArtículos de revistas


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