dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorAlmeida, RMRG
dc.creatorCruz, AJG
dc.creatorAraujo, MLGC
dc.creatorGiordano, R. C.
dc.creatorHokka, C. O.
dc.date2014-05-20T15:24:03Z
dc.date2016-10-25T17:58:08Z
dc.date2014-05-20T15:24:03Z
dc.date2016-10-25T17:58:08Z
dc.date2001-03-01
dc.date.accessioned2017-04-05T23:45:09Z
dc.date.available2017-04-05T23:45:09Z
dc.identifierApplied Biochemistry and Biotechnology. Totowa: Humana Press Inc., v. 91-3, p. 537-549, 2001.
dc.identifier0273-2289
dc.identifierhttp://hdl.handle.net/11449/34714
dc.identifierhttp://acervodigital.unesp.br/handle/11449/34714
dc.identifier10.1385/ABAB:91-93:1-9:537
dc.identifierWOS:000168567100050
dc.identifierhttp://dx.doi.org/10.1385/ABAB:91-93:1-9:537
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/878583
dc.descriptionImmobilized cell utilization in tower-type bioreactor is one of the main alternatives being studied to improve the industrial bioprocess. Other alternatives for the production of beta -lactam antibiotics, such as a cephalosporin C fed-batch p recess in an aerated stirred-tank bioreactor with free cells of Cepha-losporium acremonium or a tower-type bioreactor with immobilized cells of this fungus, have proven to be more efficient than the batch profess. In the fed-batch process, it is possible to minimize the catabolite repression exerted by the rapidly utilization of carbon sources (such as glucose) in the synthesis of antibiotics by utilizing a suitable flow rate of supplementary medium. In this study, several runs for cephalosporin C production, each lasting 200 h, were conducted in a fed-batch tower-type bioreactor using different hydrolyzed sucrose concentrations, For this study's model, modifications were introduced to take into account the influence of supplementary medium flow rate. The balance equations considered the effect of oxygen limitation inside the bioparticles. In the Monod-type rate equations, eel concentrations, substrate concentrations, and dissolved oxygen were included as reactants affecting the bioreaction rate. The set of differential equations was solved by the numerical method, and the values of the parameters were estimated by the classic nonlinear regression method following Marquardt's procedure with a 95% confidence interval. The simulation results showed that the proposed model fit well with the experimental data,and based on the experimental data and the mathematical model an optimal mass flow rate to maximize the bioprocess productivity could be proposed.
dc.languageeng
dc.publisherHumana Press Inc
dc.relationApplied Biochemistry and Biotechnology
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectcephalosperin C
dc.subjecttower-type bioreactor
dc.subjectfed-batch
dc.subjectmodeling
dc.subjectsimulation
dc.titleModeling and simulation of cephalosporin C production in a fed-batch tower-type bioreactor
dc.typeOtro


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