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  Access Rights: Use restricted to UNT Community
  Partner: UNT Libraries
 Department: Department of Biological Sciences
 Degree Discipline: Microbiology
Adherence and haemagglutination of  Moraxella catarrhalis.

Adherence and haemagglutination of Moraxella catarrhalis.

Access: Use of this item is restricted to the UNT Community.
Date: August 2000
Creator: Kosterman, Edward, III
Description: M. catarrhalis is a gram-negative diplococci frequently associated with infections of the upper respiratory tract. During the past decade, some preliminary studies have attempted to elucidate mechanisms of adherence and haemagglutination of M. catarrhalis. These studies have reported, in many cases, inconsistent results. There are two purposes of this research. First, identify mechanisms that may potentially be associated with the adherence and haemagglutination of M. catarrhalis. Second, suggest research directions that may be fruitful in clarifying these mechanisms.
Contributing Partner: UNT Libraries
BioInformatics, Phylogenetics, and Aspartate Transcarbamoylase

BioInformatics, Phylogenetics, and Aspartate Transcarbamoylase

Access: Use of this item is restricted to the UNT Community.
Date: August 2000
Creator: Cooke, Patrick Alan
Description: In this research, the necessity of understanding and using bioinformatics is demonstrated using the enzyme aspartate transcarbamoylase (ATCase) as the model enzyme. The first portion of this research focuses on the use of bioinformatics. A partial sequence of the pyrB gene found in Enterococcus faecalis was submitted to GenBank and was analyzed against the contiguous sequence from its own genome project. A BLAST (Basic Local Alignment Search Tool; Atschul, et al., 1990) was performed in order to hypothesize the remaining portion of the gene from the contiguous sequence. This allowed a global comparison to other known aspartate transcarbamoylases (ATCases) and once deduced, a translation of the sequence gave the stop codon and thus the complete sequence of the open reading frame. When this was complete, upstream and downstream primers were designed in order to amplify the gene from genomic DNA. The amplified product was then sequenced and used later in phylogenetic analyses concerning the evolution of ATCase. The second portion of this research involves taking multiple ATCase nucleotide sequences and performing phenetic and phylogenetic analyses of the archaea and eubacter families. From these analyses, ancestral relationships which dictate both structure and function were extrapolated from the data and discussed.
Contributing Partner: UNT Libraries