Office of Undergraduate Research

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Emphasizing equitable and inclusive access to research opportunities, the University of Maryland's Office of Undergraduate Research (OUR) empowers undergraduates and faculty to engage and succeed in inquiry, creative activity, and scholarship. This collection includes materials shared by undergraduate researchers during OUR events. It also encompasses materials from Undergraduate Research Day 2020, Undergraduate Research Day 2021, and Undergraduate Research Day 2022, which were organized by the Maryland Center for Undergraduate Research.

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    COMPARISON OF RIBOSWITCH REPORTER SYSTEMS FOR LIVE CELL IMAGING OF CYCLIC-DI-GMP DYNAMICS IN BACILLUS SUBTILIS POPULATIONS
    (2019) Pierre, Yasmine; Spirito, Catherine
    Fluorescent riboswitch reporters can be used in vivo to monitor metabolite dynamics. Previous work used a fluorescent yfp reporter based on a cyclic di-GMP responsive riboswitch from Bacillus licheniformis to monitor cyclic di-GMP levels in individual Bacillus subtilis cells. The previous study found that cell fates in Bacillus subtilis are not uniform in the presence of varying cyclic di-GMP levels. It is important to further develop tools that enable single-cell imaging in Gram-positive bacteria. Fluorogenic aptamers are single-stranded RNA molecules that have been evolved via in vitro selection to bind strongly and specifically to fluorophore molecules and emit a fluorescent signal. These fluorogenic aptamers can be used instead of fluorescent proteins in riboswitch reporter systems to provide a more dynamic read-out of metabolite dynamics in cells. However, relatively little work has been done to evaluate the use of these fluorogenic aptamers as reporter systems in Gram-positive bacteria. The objective of this project is to evaluate the use of four different fluorogenic aptamers (Mango-III, Broccoli, dimeric Broccoli, and SpinachII) instead of yfp in a cyclic di-GMP responsive riboswitch reporter system in Bacillus subtilis. All plasmids containing the riboswitch reporters were constructed and successfully transformed into E. coli cells. Subsequently, the cyclic di-GMP responsive riboswitch reporter systems were successfully transformed into B. subtilis WT PY79 and a 𝝙pdeH mutant. Future work involves evaluating their performance in vivo in B. subtilis via laser confocal and fluorescence microscopy.
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    Dual effect of structure and hydration on magnesium-ion insertion into electrodeposited V2O5 thin films
    (2019-10) Johnston, Brandon; Henry, Hakeem; Sahadeo, Emily; Liau, Darrin; Lee, Sang Bok; Lee, Sang Bok
    As global energy needs continue to increase, there is a growing demand for next-generation storage technologies that confer high energy density. Lithium-ion battery technologies, the current state of the art, possess a number of limitations that prevent further performance enhancement and safe use. Owing to magnesium's abundance, safety, and high volumetric capacity; magnesium-ion batteries are promising alternatives to lithium-ion storage devices. However, a number of challenges have impeded progress in magnesium-ion battery research, such as magnesium anode passivation and poor magnesium-ion insertion kinetics into traditional metal oxide cathode materials. This research addresses the latter of the two problems by further investigating a well-known potential cathode material for magnesium-ion batteries. Vanadium (V) Oxide, a transition metal oxide with flexible interlayer spacing, has been shown to reversibly intercalate Mg2+ ions with high capacity in its crystalline form. However, new research suggests that amorphous V2O5 cathodes might offer greater capacity for Mg-ion insertion owing to increased void space for monovalent and multivalent ion insertion. In this work, we use two primary electroanalytical techniques--cyclic voltammetry and galvanostatic voltammetry--to systematically investigate the impact of structure, crystallinity, and hydration on the electrochemical performance of electrodeposited V2O5 thin films. Ultimately, our findings suggest that it is structural hydration, rather than film crystallinity, that primarily determines Mg-ion insertion capacity of V2O5 thin films.