Date of Award
2016
Document Type
Thesis
Degree Name
Bachelors
Department
Natural Sciences
First Advisor
Shipman, Steven
Area of Concentration
Chemistry
Abstract
Diatoms are eukaryotic algae that mineralize an external cell wall composed of hydrated silica. This process requires diatoms to uptake soluble silicon (silicic acid) from the surrounding environment by specific silicic acid transport proteins (SITs). This family of proteins is relatively uncharacterized. The goal of this project was to 1) express and purify SIT1 from the diatom Phaeodactylum tricornutum (PtSIT1), 2) reconstitute the protein into a synthetic lipid vesicle and to 3) determine whether SIT1 can behave as a silicic acid transporter in vivo for eventual applications in nanotechnology. PtSIT1 was overexpressed in yeast and purified in the solubilizing detergent Fos-choline 12. The purified protein was successfully reconstituted into synthetic liposomes and silicic acid uptake was assessed using a fluorescent assay which used zinc silicate fluorescence. This method also was used to determine that silicic acid transported by PtSIT1 displayed Michaelis-Menten kinetics with a Km of 1.48 μM. Preliminary electron microscopy suggested that the silicic acid silicic acid transported into the liposome condense to form silica nanoparticles in the presence of tetraethylenepentamine, a condensing agent. This work confirms that PtSIT1 can be utilized in further exploration of biomineralization of silica in vivo in an effort to explore ‘green’ syntheses of silica nanoparticles.
Recommended Citation
Kirk, Brenna, "PtSIT1: PROTEIN FUNCTION IN SILICIC ACID TRANSPORT FOR BIOMIMETIC SILICA SYNTHESIS" (2016). Theses & ETDs. 5231.
https://digitalcommons.ncf.edu/theses_etds/5231