dc.contributorNovo-Mansur, Maria Teresa Marques
dc.contributorhttp://lattes.cnpq.br/1198926223396748
dc.contributorGoto, Leandro Seiji
dc.contributorhttp://lattes.cnpq.br/1241086430897870
dc.contributorhttps://lattes.cnpq.br/8241037351836089
dc.creatorCandido, Camila Escobar
dc.date.accessioned2023-04-12T13:00:44Z
dc.date.accessioned2023-09-04T20:26:45Z
dc.date.available2023-04-12T13:00:44Z
dc.date.available2023-09-04T20:26:45Z
dc.date.created2023-04-12T13:00:44Z
dc.date.issued2023-03-31
dc.identifierCANDIDO, Camila Escobar. Construção de vetor plasmidial para deleção gênica da ORF XAC3162 de Xanthomonas citri subsp.citri. 2023. Trabalho de Conclusão de Curso (Graduação em Biotecnologia) – Universidade Federal de São Carlos, São Carlos, 2023. Disponível em: https://repositorio.ufscar.br/handle/ufscar/17705.
dc.identifierhttps://repositorio.ufscar.br/handle/ufscar/17705
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8630341
dc.description.abstractCitrus canker is a bacterial disease caused by Xanthomonas citri (XAC), which affects all citrus species and causes damage to fruit quality and productivity. In 2022, in Brazil, the world´s largest producer of oranges, the disease presented a high rate of dissemination. The production of β- lactamases by XAC may contribute to its defense against microorganisms, including endophytes, which can secrete β-lactam antibiotics. The gene XAC3162, which is annotated as a β-lactamase in XAC, is an interesting gene to investigate its possible contribution to XAC pathogenicity. This work aimed to obtain a recombinant vector for deletion of XAC3162 gene from XAC genome by double homologous recombination. The l kb upstream and downstream regions of the XAC3162 gene were cloned into the pJET1.2 vector for propagation and subcloned in tandem into the suicide vector pNPTS138, which encodes for kanamycin resistance. Vector construction was successfully performed, as indicated by enzymatic digestion followed by SDS-PAGE. Electroporation of XAC did not yield kanamycin-resistant transformants, despite of several attempts performed under different conditions. More investigations will be needed in the future to elucidate why XAC3162 gene is refractory to deletion by homologous recombination.
dc.languagepor
dc.publisherUniversidade Federal de São Carlos
dc.publisherUFSCar
dc.publisherCâmpus São Carlos
dc.publisherBiotecnologia - Biotec
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/br/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Brazil
dc.subjectXanthomonas citri subsp citri
dc.subjectXAC3162
dc.subjectβ-lactamase
dc.subjectRecombinação homóloga
dc.subjectHomologous recombination
dc.titleConstrução de vetor plasmidial para deleção gênica da ORF XAC3162 de Xanthomonas citri subsp.citri
dc.typeTCC


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