Optimizing the heterologous expression of human O-GlcNAcase and the following isolation procedures.

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dc.contributor.advisorBarna, Teréz
dc.contributor.authorLuu, Thanh Sinh
dc.contributor.departmentDE--Természettudományi és Technológiai Kar--Biológiai és Ökológiai Intézethu_HU
dc.date.accessioned2019-11-22T07:43:54Z
dc.date.available2019-11-22T07:43:54Z
dc.date.created2019-11-19
dc.description.abstractO-ClcNAc is an important post-translational modification of various proteins. The removal of O-GlcNAc is catalyzed by human O-GlcNAcase enzyme. The thesis work aimed to optimize the heterologous expression of human O-GlcNAc in E. coli. The growth condition turned out to affect protein formation significantly. The isolation was developed by combining different compounds, showing interesting behaviours of the enzyme.hu_HU
dc.description.courseBiochemical Engineeringhu_HU
dc.description.degreeBSc/BAhu_HU
dc.format.extent43hu_HU
dc.identifier.urihttp://hdl.handle.net/2437/276651
dc.language.isoenhu_HU
dc.subjectEnzymehu_HU
dc.subjectProteinhu_HU
dc.subject.dspaceDEENK Témalista::Biológiai tudományokhu_HU
dc.titleOptimizing the heterologous expression of human O-GlcNAcase and the following isolation procedures.hu_HU
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Theses (Faculty of Science and Technology)