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dc.contributor.authorBennett, Nicholas James
dc.date.accessioned2010-03-31T21:25:40Z
dc.date.availableNO_RESTRICTIONen_US
dc.date.available2010-03-31T21:25:40Z
dc.date.issued2010-03-31T21:25:40Z
dc.identifier.urihttp://hdl.handle.net/10179/1221
dc.descriptionEmbargoed until 1 January 2012
dc.description.abstractFf filamentous bacteriophage infect male (F+) strains of Escherichia coli and are assembled at the cell membranes, by a secretion-like, non-lethal process. The pIII protein, located at one end of the virion-filament, is required at both the beginning and the end of the phage life cycle. During infection, the N-terminal domains of pIII, N2 and N1, bind to the primary and secondary host receptors, F pilus and TolA protein, respectively. At the end of the life cycle, the pIII C-domain mediates the termination and release of virions. Thus, both entry and release involve structural transitions of the virus coupled to membrane transactions of the virion proteins. "Unlocking” of the highly stable virion presumably results in membrane integration during entry, whereas a reverse event, “locking” of the virion, occurs upon detachment from the membrane at termination step of assembly/secretion. Recently, it was shown that the pIII C-domain plays an active role at the step of entry. This finding implicates the C-domain of pIII in “unlocking” of the virion, presumably resulting in the exposure of the membrane anchor at the very C-terminus of pIII (Bennett & Rakonjac, 2006). To further this work, this thesis has mapped the portion of the pIII C-domain required for infection, by constructing a set of nested deletions of the C-domain fused to the receptor binding domains N1 and N2, and then determined the infectivity of phage carrying the mutant proteins. This mapped the portion of the C-domain required for phage infection is different to that required for termination of assembly. The different requirement for entry and release suggests that the two processes are carried out by distinct mechanisms and/or depend on different sets of accessory proteins. In addition, a system was designed for the efficient production and purification of very short virions, the length of which is 1/20 that of the wild-type f1. These short virions, called microphage, are the first step towards the structural analyses of the phage termini cap structures, of which one contains pIII in the “locked” conformation.en_US
dc.language.isoenen_US
dc.publisherMassey Universityen_US
dc.rightsThe Authoren_US
dc.subjectFilamentous bacteriophageen_US
dc.subjectMicrophage production systemen_US
dc.subject.otherFields of Research::270000 Biological Sciences::270100 Biochemistry and Cell Biologyen_US
dc.titleUnlocking the M13 (f1 and fd) virion : investigation into the role of the pIII C-domain of F specific filamentous bacteriophage in infection : a thesis presented in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Biochemistry at Massey University, Palmerston North, New Zealand.en_US
dc.typeThesisen_US
thesis.degree.disciplineBiochemistryen_US
thesis.degree.grantorMassey Universityen_US
thesis.degree.levelDoctoralen_US
thesis.degree.levelDoctoralen
thesis.degree.nameDoctor of Philosophy (Ph.D.)en_US


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