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dc.contributor.authorMohd Sairi, Mohd Fareed
dc.date.accessioned2015-07-28
dc.date.available2015-07-28
dc.date.issued2015-03-31
dc.identifier.urihttp://hdl.handle.net/2123/13617
dc.description.abstractMolluscan rhogocyte cells are known to synthesise the largest respiratory proteins in nature known as hemocyanin. However, attempt to investigate the cells in vitro to understand the hemocyanin biosynthesis is difficult due to the lack of current knowledge on establishing a stable cell culture. Therefore, the aims of this study were to isolate rhogocyte cells from Haliotis laevigata and assessed their characteristics, distribution, capability to grow and synthesise hemocyanin in vitro. Using flow cytometry analysis and simultaneous staining of immunofluorescence and in situ hybridisation strategy, two distinct populations of rhogocyte cells synthesizing type 1 hemocyanin was determined in the mantle tissue. Subsequently, a primary culture of heterogeneous cells was established with different parameters involving basal media, primary growth supplements, secondary growth supplements, growth temperature and seeding density. Cells cultured in MEM result in the highest cell yield compared to other basal media. It is suggested that the presence of vitamin B6 in aldehyde form (pyridoxal) instead of alcohol (pyridoxine) is responsible for promoting the cellular activity. Furthermore, addition of lipimax at 17°C resulted in higher cell-fold increase compared to FBS, knockout serum and hemolymph. Addition of secondary supplements such as amino acids cocktail, lipid concentrate, insulin-transferrin-selenium and vitamin concentrate, however, had no significant impact on the cell growth. On the other hand, evaluation of hemocyanin content using ELISA revealed significant increase of hemocyanin in the media when cells were cultured with lipimax, FBS and knockout serum. However, the hemocyanin content was at the highest concentration only after an hour of culture before decreasing significantly and stabilised around 0.14-0.16 µg/ml in the media. These results suggest that hemocyanin biosynthesis may have an inverse correlation with the cell’s growth.en_AU
dc.rightsThe author retains copyright of this thesis. It may only be used for the purposes of research and study. It must not be used for any other purposes and may not be transmitted or shared with others without prior permission.en_AU
dc.subjectabaloneen_AU
dc.subjectHaliotis laevigataen_AU
dc.subjectflow cytometryen_AU
dc.subjectflow countingen_AU
dc.subjectimmunofluorescenceen_AU
dc.subjectfluorescence in situ hybridisation (FISH)en_AU
dc.subjecthemocyaninen_AU
dc.subjecthemocyanin biosynthesisen_AU
dc.subjectrhogocyte cellen_AU
dc.titleIsolation of cells from a Marine Source Responsible for Hemocyanin Biosynthesisen_AU
dc.typeThesisen_AU
dc.date.valid2015-01-01en_AU
dc.type.thesisDoctor of Philosophyen_AU
usyd.facultyFaculty of Engineering and Information Technologies, School of Chemical and Biomolecular Engineeringen_AU
usyd.degreeDoctor of Philosophy Ph.D.en_AU
usyd.awardinginstThe University of Sydneyen_AU


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