Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/68471
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dc.contributor.authorKoh, Zhong Ren-
dc.date.accessioned2016-05-26T04:09:53Z-
dc.date.available2016-05-26T04:09:53Z-
dc.date.issued2016-
dc.identifier.urihttp://hdl.handle.net/10356/68471-
dc.description.abstractWith the potential of Archaeoglobus fulgidus ferritin to serve as an MRI contrast agent, the study sought to optimize ferritin and feoB production using arabinose induction and to optimize in vivo iron loading in strains of engineered E. coli. The plasmid pBbE8k was primarily used as a vector for ferritin and feoB genes. Arabinose induction for feoB was roughly optimized at 0.1 mM. However, narrower optimization and repeatability studies are highly recommended in future. The AfFtn gene in pBbE8k failed to be expressed although many efforts were taken to resolve this issue throughout the course of the year. Nevertheless, the expression of IPTG-induced AfFtn in pET-11a was achieved and the results of the Bradford Assay, Iron Colorimetric Assay, and Dynamic Light Scattering for this strain serve as a point of reference for the pBbE8k strain. The re-cloning of RBS and ferritin gene onto pBbE8k by varied methods is highly recommended in order to make progress in this ongoing effort.en_US
dc.format.extent51 p.en_US
dc.language.isoenen_US
dc.rightsNanyang Technological University-
dc.subjectDRNTU::Science::Chemistry::Analytical chemistry::Proteinsen_US
dc.subjectDRNTU::Engineering::Bioengineeringen_US
dc.subjectDRNTU::Science::Biological sciences::Microbiology::Bacteriaen_US
dc.subjectDRNTU::Science::Biological sciences::Geneticsen_US
dc.titleEngineering E. coli for the biosynthesis of nanoparticlesen_US
dc.typeFinal Year Project (FYP)en_US
dc.contributor.supervisorLim Sierinen_US
dc.contributor.schoolSchool of Chemical and Biomedical Engineeringen_US
dc.description.degreeBachelor of Engineering (Chemical and Biomolecular Engineering)en_US
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Appears in Collections:SCBE Student Reports (FYP/IA/PA/PI)
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