2008 Proceedings - St. Cloud State University
2008 Proceedings - St. Cloud State University
2008 Proceedings - St. Cloud State University
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Abstracts<br />
Session T All Disciplines Ballroom<br />
Atmospheric Wind Interferometer Characterization<br />
Upper atmospheric wind measurements are valuable in gaining a better understanding of upper atmospheric dynamics. As part of a NASA<br />
funded program we are developing a laboratory prototype of a small, rugged optical instrument that may eventually be capable of<br />
measuring atmospheric winds from a satellite platform. The instrument contains a Spatial Heterodyne Spectrometer which produces<br />
interference fringes. Measuring the phase of these fringes allows us to determine the wind speed. The accuracy of measuring the fringe<br />
phase, and therefore the wind speed, is limited by practical difficulties such as thermal drift of the instrument and the finite signal-to-noise<br />
ratio of the measured fringe pattern. In this poster we will describe our laboratory set-up for generating interference fringes and tests of<br />
how accurately the fringe phase can be measured. We will also compare our phase precision results with a theoretical model.<br />
Presentation Index: T43<br />
Time: 2:00 p.m.<br />
Department: Physics<br />
Project Sponsor(s):<br />
<strong>St</strong>udent Presenter(s): Fuchs, Brody<br />
Harlander, John<br />
Investigations of Temperature Dependence of Charge Carrier Mobilities<br />
While organic semiconductors have started to be used in commercial devices, their full potential will not be realized without further<br />
characterization of their charge carrier transport properties. To understand these properties the temperature dependence of the charge<br />
carrier mobility needs to be investigated. At low temperatures, charge carriers are not associated with a particular molecule and band-like<br />
transport occurs. As temperatures increase, thermal motion perturbs the path of the charge carriers and mobilities decrease. Mobilities<br />
also decrease at extremely low temperatures due to the presence of traps. When the thermal energy of the charge carrier is less then the<br />
trapping energies the charge carrier mobility falls off sharply. Finally, at higher temperatures the charge carriers become thermally<br />
activated and ‗jump‘ from molecule to molecule resulting in a hopping transport mechanism which increases the mobility. In our research,<br />
we study temperature dependant mobilities using a time of flight technique in a helium cryostat to gain a better understand of these<br />
transport mechanisms.<br />
Presentation Index: T44<br />
Time: 2:00 p.m.<br />
Department: Physics<br />
Project Sponsor(s):<br />
<strong>St</strong>udent Presenter(s): Pundsack, Thomas; Haugen, Neale<br />
Lidberg, Russell<br />
The First Annotation of the Valine, Leucine and Isoleucine Biosynthetic Pathways of Ammonifex Degensii<br />
Ammonifex degensii is an obligate anaerobic chemolithoautotrophic (obtains energy from inorganic compounds and carbon from CO2)<br />
bacteria isolated from a volcanic hot spring in East Asia in 1994. Ammonifex is the archetype of a new genus (¡°ammonium maker¡±).<br />
Ammonifex degensii is an extremely thermophilic gram negative rod shaped bacterium with optimal growth occurring at 70¢ªC and a pH of<br />
7.5. The genome of Ammonifex degensii is 85% complete, funded by the Department of Energy Joint Genome Program. Saint <strong>Cloud</strong> <strong>St</strong>ate<br />
<strong>University</strong> is part of a consortium of institutions that make up the Collaborative Undergraduate Genomic Annotation Team. SCSU has<br />
undertaken the responsibility of using comparative genomics to identify the amino acid biosynthetic pathways. Valine, isoleucine and<br />
leucine are three nonpolar aliphatic amino acids. Valine is the smallest of the three, while leucine and isoleucine represent very similar<br />
amino acids. We hypothesize that these amino acids have biosynthetic pathways in Ammonifex degensii, and that we will be able to<br />
identify the genes responsible for the synthesis of these amino acids using a comparative genomics approach.<br />
Presentation Index: T45<br />
Time: 2:00 p.m.<br />
Department: Biological Sciences<br />
Project Sponsor(s):<br />
<strong>St</strong>udent Presenter(s): Piotrowski, Aaron; Perera, Deshani; Shrestha, Sharad;<br />
Kvaal, Christopher<br />
Gast, Dawn<br />
Antiviral Chemotherapeutics from Natural Products: <strong>St</strong>rategic Design, Designed Synthesis & Characterization of a New Series of<br />
Bioactive Triterpenoids<br />
From ancient period, it is well known that Natural Products and their Extracts are widely used for treatment and curing of several common human<br />
and animal diseases. Modern research and development in Natural Products Chemistry have shown the bright perspectives of their pre-clinical<br />
and clinical use as potential antiviral and antibacterial agents. Recent biological studies of some Triterpene based natural products revealed<br />
remarkable biological activity and other valuable pharmacological properties. For instance, Betulinic Acid and Betulin 3-caffeate exhibited strong<br />
anti-HIV and anti-Cancer activity in vitro and in vivo, and identified them as a new class of potential anti-cancer and anti-HIV agents with a novel<br />
mechanism of antiviral action. The ultimate goal of our multifaceted research project is to study and develop a thorough pathway of strategic<br />
design, designed synthesis, modification, characterization and bioactivity evaluation for a new series of highly efficacious triterpenoid based<br />
antiviral chemotherapeutics of novel drug action. At a relatively earlier stage, as an integral part of the project, deliberately we will be focused on<br />
Betulinic Acid. A novel method for semi-synthesis of Betulinic acid will be discussed. A new pathway for selective Protection and Selective<br />
Functionalization of Betulinic Acid will be demonstrated. <strong>St</strong>rategic Design for Selective Derivatization and <strong>St</strong>ructure-Activity Relation (SAR) will be<br />
illustrated. And, several new synthetic methodologies for preparing Betulinic Acid Derivatives will be outlined.<br />
Presentation Index: T46<br />
Time: 2:00 p.m.<br />
Department: Chemistry<br />
Project Sponsor(s):<br />
<strong>St</strong>udent Presenter(s): Shrestha, Sharad; Manandhar, Sonal<br />
Munshi, Kaylan<br />
<strong>St</strong>. <strong>Cloud</strong> <strong>St</strong>ate <strong>University</strong> <strong>St</strong>udent Research Colloquium 63<br />
April 22, <strong>2008</strong>