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                <text>Two lines of Arabidopsis thaliana are studied in Dr Breeze’s lab. One is GFP-HDEL which is a control line of Arabidopsis, whilst the other is GFP-CXN a genetically modified line that overexpresses a domain of chaperone protein called calnexin in its endoplasmic reticulum (ER). This causes GFP-CXN to have a highly interconnected network of flattened, membrane-enclosed sacs in its ER known as cisternae. The cisternae have a crucial role in the modification of proteins.&#13;
It has been suggested in previous studies that whilst challenging the lines with the plant pathogen Pseudomonas syringae DC3000 the GFP-CXN line has been less susceptible to infection than the control potentially due to the ER’s highly cisternal morphology. However, to support this hypothesis further characterization of GFP-CXN is required.• The aim of my project was to further characterize the GFP-CXN line by investigating chloroplast efficiency/function during infection by measuring Fv/Fm, image ER morphology in a confocal microscope, compare bacterial susceptibility by completing a bacterial growth assay and investigate physiology by measuring and comparing root&#13;
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                <text>The aim of this project is to evaluate the chemical stability of OER electrodes by understanding the effects of different variables. Two different substrates,&#13;
namely, hematite and titanium were tested. A ruthenium electrocatalyst was deposited onto both surfaces, which were studied in different electrolytes to realize the optimal pH for their performance. Additionally, the effect of a varied overpotential was determined.</text>
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