Comparison of multi-gene integration strategies in CRISPR-based transformation of Saccharomyces cerevisiae

dc.contributor.advisorden Haan, Riaan
dc.contributor.authorJacob, Odwa
dc.date.accessioned2022-03-24T09:44:45Z
dc.date.accessioned2024-05-09T07:46:06Z
dc.date.available2022-03-24T09:44:45Z
dc.date.available2024-05-09T07:46:06Z
dc.date.issued2021
dc.description>Magister Scientiae - MScen_US
dc.description.abstractSaccharomyces cerevisiae is an important host in industrial biotechnology. This yeast is the host of choice for the first and second-generation biofuels for ethanol production. Genome modification in S. cerevisiae has been extremely successful largely due to this yeast’s highly efficient homology-directed DNA repair machinery. The advent of CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) genome editing technology has made multi-gene editing in yeast more accessible. In this study, we aimed at targeting the Cas9 to multiple genomic positions for integrating multiple genes at different sites. We have developed two CRISPR-Cas9 systems, based on published one- and two-plasmid systems, for application in S. cerevisiae strains. In this study, these CRISPR-Cas9 systems were used to transform fungal heterologous genes into yeast using the electroporation transformation method.en_US
dc.identifier.urihttps://hdl.handle.net/10566/13391
dc.language.isoenen_US
dc.publisherUniversity of Western Capeen_US
dc.rights.holderUniversity of Western Capeen_US
dc.subjectIndustrial biotechnologyen_US
dc.subjectYeasten_US
dc.subjectCRISPR-Cas9 systemsen_US
dc.subjectT.r.eg2 geneen_US
dc.subjectSaccharomyces cerevisiaeen_US
dc.titleComparison of multi-gene integration strategies in CRISPR-based transformation of Saccharomyces cerevisiaeen_US

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