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Study of the intracellular function of the Salmonella enterica serovar Typhimurium type III secretion effector SspH1 /Haraga, Andrea. January 2005 (has links)
Thesis (Ph. D.)--University of Washington, 2005. / Vita. Includes bibliographical references (leaves 78-87).
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Synthesis and characterization of phosphono-CheY from Thermotoga maritima /Haas, R. Matthew January 2007 (has links)
Thesis (M.S.)--University of North Carolina Wilmington, 2007. / Includes bibliographical references (leaves: 190-193)
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Comparison of protein OprF from Pseudomonas syringae with protein OprF from Pseudomonas aeruginosaUllstrom, Catherine Ann MacDonald January 1990 (has links)
The major outer membrane protein OprF from Pseudomonas aeruginosa was compared with OprF from the fluorescent phytopathogen Pseudomonas syringae. The P. syringae oprF gene was subcloned and sequenced and found to code for a sequence of 344 amino acids containing a 24 amino acid leader sequence. The mature protein, with a deduced molecular weight of 34,225, contained four cysteine residues and an alanine-proline rich area. Comparison of the P. syringae OprF amino acid sequence with the P. aeruginosa OprF and the E. coli OmpA sequences showed that the sequences were most similar at the carboxy-terrninal ends. Restriction enzyme site heterogeneity near the oprF gene from nine different P. syringae pathovars was determined. All pathovars had a conserved SalI site within the gene and conserved PstI. and BamHI sites near the ends of the gene. The location of the PstI and the SalI sites outside the gene was variable, although similar. Immunological relatedness between P. syringae OprF from the different pathovars and P. aeruginosa OprF was confirmed. Protein OprF from all the pathovars was shown to be 2-mercaptoethanol modifiable and more easily heat modifiable than was OprF from P. aeruginosa. / Science, Faculty of / Microbiology and Immunology, Department of / Graduate
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Folding kinetics and redesign of Peptostreptococcal protein L and G /Nauli, Sehat. January 2003 (has links)
Thesis (Ph. D.)--University of Washington, 2003. / Vita. Includes bibliographical references (leaves 78-86).
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The study of the Escherichia coli BarA-UvrY two-component system and its ability to sense the environment /Pernestig, Anna-Karin, January 2002 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst., 2003. / Härtill 4 uppsatser.
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Bacillus subtilis GlpP protein, antitermination and mRNA stabilityGlatz, Elisabeth. January 1998 (has links)
Thesis (doctoral)--Lund University, 1998. / Added t.p. with thesis statement inserted. Includes bibliographical references.
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Alpha C protein of group B Streptococcus as a potential vaccine candidatePannaraj, Pia S. Baker, Carol J. Aragaki, Corinne Pedroza, Claudia January 2007 (has links)
Source: Masters Abstracts International, Volume: 46-04, page: 2101. Adviser: Carol J. Baker. Includes bibliographical references.
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Bacillus subtilis GlpP protein, antitermination and mRNA stabilityGlatz, Elisabeth. January 1998 (has links)
Thesis (doctoral)--Lund University, 1998. / Added t.p. with thesis statement inserted. Includes bibliographical references.
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Variability of tprK and the immune response to tprK variants during Treponema pallidum infection /LaFond, Rebecca E. January 2006 (has links)
Thesis (Ph. D.)--University of Washington, 2006. / Vita. Includes bibliographical references (leaves 147-179).
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Structural basis for transcription regulations in Mycobacterium tuberculosis by iron-dependent regulator and dormancy survival regulator /Wisedchaisri, Goragot. January 2005 (has links)
Thesis (Ph. D.)--University of Washington, 2005. / Vita. Includes bibliographical references (leaves 232-250).
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