Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/39981
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dc.contributor.authorTay, Shawn Wei Liang.
dc.date.accessioned2010-06-08T09:10:23Z
dc.date.available2010-06-08T09:10:23Z
dc.date.copyright2010en_US
dc.date.issued2010
dc.identifier.urihttp://hdl.handle.net/10356/39981
dc.description.abstractThe FK-506 binding proteins (FKBPs) are a family of proteins with characterised molecular functions such as peptidylprolyl cis-trans isomerase activity and chaperone activity. However, the FKBP family member from Pseudomonas aeruginosa is currently uncharacterised. This study has successfully developed a recombinant method of overexpressing and purifying the FK-506 binding domain of P. aeruginosa (PaFKBD) in a SUMO-PaFKBD fusion protein state. The characterisation of SUMO-PaFKBD revealed peptidylprolyl cis-trans isomerase activity with catalytic efficiency of 1.01 x 105 s-1 M-1 and this activity is inhibited by FK-506 with an IC50 of 92.6nM. More studies need to be done to further reaffirm these results and to further characterise the protein.en_US
dc.format.extent42 p.en_US
dc.language.isoenen_US
dc.rightsNanyang Technological University
dc.subjectDRNTU::Science::Biological sciences::Biochemistryen_US
dc.titleMolecular cloning, expression, purification and characterization of a recombinant FKBP family member from Pseudomonas aeruginosa.en_US
dc.typeFinal Year Project (FYP)en_US
dc.contributor.supervisorYoon Ho Supen_US
dc.contributor.schoolSchool of Biological Sciencesen_US
dc.description.degreeBachelor of Science in Biological Sciencesen_US
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Appears in Collections:SBS Student Reports (FYP/IA/PA/PI)
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