Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/34086
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dc.contributor.authorBento, Heitorpt_PT
dc.contributor.authorPaiva, Gabrielapt_PT
dc.contributor.authorPedrolli, Daniellept_PT
dc.contributor.authorCarvalho, Pedropt_PT
dc.contributor.authorSilva, Claudiapt_PT
dc.contributor.authorTavares, Ana Paulapt_PT
dc.contributor.authorSantos-Ebinuma, Valériapt_PT
dc.date.accessioned2022-06-29T15:14:03Z-
dc.date.available2022-06-29T15:14:03Z-
dc.date.issued2022-04-07-
dc.identifier.urihttp://hdl.handle.net/10773/34086-
dc.description.abstractThermal kinetic analysis is one of the main factors to establish a biopharmaceutical application. L-Asparaginase is an important enzyme for the pharmaceutical industry due to its application in the treatment of some lymphoid malignancies as acute lymphoblastic leukemia. Novel recombinant enzymes may be the solution in order to reduce or eliminate the side effects showed by the commercial preparations. The objective of the present study is to evaluate the thermal kinetic of a novel recombinant Aliivibrio fischeri L-Asparaginase produced by engineered Bacillus subtilis. Cultivations were carried out in orbital shaker using 500 mL Erlenmeyer flasks containing 100 mL of Luria-Bertani medium, at 30 ºC, 200 rpm for 24 h. Cells were recovered by centrifugation and submitted to sonication for cell lysis. Enzymatic extract was evaluated at 25 ºC, 37 ºC, 45 ºC and 60 ºC considering the enzymatic activity over times. L- Asparaginase activity was measured according the ammonium release in L-Asparagine hydrolysis. Thermal parameters were calculated considering a single and a consecutive reactions model. Models analysis indicated that enzyme thermal inactivation follow a single reaction model, where k values of 0.128 h-1, 0.148 h-1, 0.262 h-1, 0.701 h-1 and 1.187 h-1 were obtained for 25 ºC, 37º, 45 ºC and 60 ºC, respectively. The enzymatic extract showed a half life time of 13 h at 25 ºC and 5 h at 37 ºC, indicating the product have satisfactory properties at room temperature and at human body temperature. The results herein showed the analyzed recombinant L-Asparaginase have potential to be used as a biopharmaceutical.pt_PT
dc.language.isoengpt_PT
dc.relationPOCI-01-0145-FEDER-031268pt_PT
dc.relationFAPESP: 2018/06908-8pt_PT
dc.relationFAPESP: 2020/15513-7pt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectThermal kineticpt_PT
dc.subjectBiopharmaceuticalpt_PT
dc.subjectL-Asparaginasept_PT
dc.titleThermal kinetic analusis of aliviibrio fischeri recombinant L-Asparaginasept_PT
dc.typeconferenceObjectpt_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
ua.event.date7-9 abril, 2022pt_PT
degois.publication.firstPage247pt_PT
degois.publication.title3º Bio IberoAmérica - Congresso Ibero-Americano de Biotecnologiapt_PT
dc.relation.publisherversionhttps://www.bioiberoamerica2022.com/pt/resumospt_PT
Appears in Collections:CICECO - Comunicações
DQ - Comunicações

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