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The construction of lambda phages containing both ends of Mu and their use in analysis of bacteriophage Mu transpositionSchumm, James W. January 1981 (has links)
Thesis (Ph. D.)--University of Wisconsin--Madison, 1981. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 214-227).
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Bacteriophage typing of Salmonella pullorumCastellano, Gabriel Angelo January 2011 (has links)
Typescript, etc. / Digitized by Kansas State University Libraries
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An evaluation of the phage amplification assay for detection of salmonellaSilva de Siqueira, Regina January 2003 (has links)
No description available.
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Molecular genetic analysis of the phage growth limitation (Pgl) system of Streptomyces coelicolor A3(2)Bedford, David Jonathan January 1994 (has links)
No description available.
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A DNA packaging system from the Streptomyces phage #phi#C31Finnis, Christopher J. A. January 2002 (has links)
No description available.
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Effect of multiplicity of infection on m-RNA synthesis in Escherichia coli cells infected by bacteriophage lambda.January 1976 (has links)
Yin-ping Yu. / Thesis (M. Phil.)--Chinese University of Hong Kong. / Bibliography: l. 126-137.
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Studies on staphylococcal typing phagesFarrant, Robert Kennion. January 1970 (has links) (PDF)
No description available.
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Bacteriophage ms2 l protein: genetic and biochemical characterizationMcIntosh, Brenley Kathleen 15 May 2009 (has links)
In order to release progeny, bacteriophages must lyse the host cell by compromising the peptidoglycan layer. There are two known strategies of lysis: the holin-endolysin system and single gene lysis (SGL), which are dependent on the genome size. Large phages encode multiple proteins, including a holin and endolysin, for lysis. In contrast, small ssRNA phages (Leviviridae and Alloleviviridae) and ssDNA phages (Microviridae) do not encode a muralytic enzyme and accomplish lysis with a single gene. The cellular target of the lysis gene E from the prototypic microvirus, φX174, and A2 from the prototypic allolevivirus, Qβ, has been elucidated. In both cases, these proteins were demonstrated to inhibit specific enzymes within the peptidoglycan biosynthetic pathway and infected cells lyse as a result of septal catastrophes. The prototype Levivirus MS2 encodes L, a 75 aa polypeptide that effects lysis without inhibiting murein synthesis. The purpose of the work described in this dissertation was to characterize MS2 L using genetic and biochemical strategies. Using a genetic approach, PcnB was shown to be important to the entry of the MS2 RNA into the cytoplasm. L accumulation during infection was quantified by comparison to purified, oligohistidine-tagged L. Biochemical experiments demonstrated the L protein behaved as a periplasmic, membrane-associated protein. The morphologies of cells undergoing L-mediated lysis are significantly different from cells lysing due to A2 expression, since L-lysing cells do not show septally localized membrane protrusions.
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Bacteriophage ms2 l protein: genetic and biochemical characterizationMcIntosh, Brenley Kathleen 15 May 2009 (has links)
In order to release progeny, bacteriophages must lyse the host cell by compromising the peptidoglycan layer. There are two known strategies of lysis: the holin-endolysin system and single gene lysis (SGL), which are dependent on the genome size. Large phages encode multiple proteins, including a holin and endolysin, for lysis. In contrast, small ssRNA phages (Leviviridae and Alloleviviridae) and ssDNA phages (Microviridae) do not encode a muralytic enzyme and accomplish lysis with a single gene. The cellular target of the lysis gene E from the prototypic microvirus, φX174, and A2 from the prototypic allolevivirus, Qβ, has been elucidated. In both cases, these proteins were demonstrated to inhibit specific enzymes within the peptidoglycan biosynthetic pathway and infected cells lyse as a result of septal catastrophes. The prototype Levivirus MS2 encodes L, a 75 aa polypeptide that effects lysis without inhibiting murein synthesis. The purpose of the work described in this dissertation was to characterize MS2 L using genetic and biochemical strategies. Using a genetic approach, PcnB was shown to be important to the entry of the MS2 RNA into the cytoplasm. L accumulation during infection was quantified by comparison to purified, oligohistidine-tagged L. Biochemical experiments demonstrated the L protein behaved as a periplasmic, membrane-associated protein. The morphologies of cells undergoing L-mediated lysis are significantly different from cells lysing due to A2 expression, since L-lysing cells do not show septally localized membrane protrusions.
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Genetic and biochemical characterization of suppressors in the self-splicing nrdB intron of bacteriophage T4Ranganathan, Srikanth 08 1900 (has links)
No description available.
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