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dc.contributor.advisorLe Roes-Hill, Marilize
dc.contributor.advisorMcCullough, Bronwyn Kirby
dc.contributor.authorGroep, Juandré
dc.date.accessioned2024-07-29T13:30:44Z
dc.date.available2024-07-29T13:30:44Z
dc.date.issued2024
dc.identifier.urihttp://hdl.handle.net/11394/10835
dc.description>Magister Scientiae - MScen_US
dc.description.abstractTwenty-one whole genome actinobacterial sequences were obtained from strains previously isolated from various environments. A genome-mining approach was applied to identify the presence of Dye-decolourising (DyP-type or DyPs) peroxidases. From genome sequence annotation twenty-six DyP-type sequences were identified and through bioinformatic analysis for the presence of twin-arginine translocation (Tat) pathway signal peptides, was classified as belonging to class I (formerly class A) bacterial DyP-type peroxidases. Phylogenetic analysis of the DyP sequences showed that the Streptomyces derived DyPs were predominantly grouping together and the nonStreptomyces derived DyPs followed the same pattern. Eight DyP-type peroxidases were selected for cloning, with the majority being derived from Streptomyces spp., and primers were designed to amplify the DyP-type peroxidase genes. The PCR-amplicons were subjected to restriction digests and were ligated into pET20b(+). The constructs were transformed into Escherichia coli JM109.en_US
dc.language.isoenen_US
dc.publisherUniversity of the Western Capeen_US
dc.subjectActinobacteriaen_US
dc.subjectperoxidaseen_US
dc.subjectDye-decoloursing peroxidaseen_US
dc.subjectDyP-typeen_US
dc.subjectdecolourisationen_US
dc.titleNovel DyP-type peroxidases from actinobacteria: a genome mining approachen_US
dc.rights.holderUniversity of the Western Capeen_US


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