Use this URL to cite or link to this record in EThOS:
Title: Quantitative characterisation of morphological and phenotypic changes during microbial cell differentiation and multicellular behaviour
Author: Porter, Michael
Awarding Body: University of Dundee
Current Institution: University of Dundee
Date of Award: 2020
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Thesis embargoed until 31 May 2023
Access from Institution:
Bacteria inhabit almost every conceivable niche on the planet and have evolved adaptations that confer fitness to one or a number of environments. Because of these adaptations, some species of bacteria are successful living in such different environments as the root of a plant and in the gut of a human. One such species is Bacillus subtilis and, as it is non-pathogenic, makes it an ideal organism to use in the study of bacterial environmental adaptation. It is a motile, Gram-positive, endospore-forming bacterium that can live swimming in liquid or can form communities of cells – termed biofilms - in a self-produced extracellular matrix either floating on top of a liquid or sitting on a solid surface. In this work I will detail publications, to which I contributed, covering the differentiation and regulation of B. subtilis, looking at molecules governing gene activation and silencing during the transition from one growth environment to another, and the effect this has on the production of excreted molecules that modify the cells’ local environment to aid in community, rather than planktonic, growth. I will also describe my latest research using microscopical methods to examine and quantify multicellular behaviours of B. subtilis in three distinct phases of the development of colony biofilms. These methods include monitoring expression of a fluorescent reporter for an operon whose gene products produce the polysaccharide component of the extracellular matrix, and doing so with strains deficient in the major matrix component genes results in establishing that regulation of this gene network is inter-dependant on the matrix as a whole. Furthermore, following the types of motion displayed by the cells of matrix mutant strains by time-lapse microscopy, and employing still-image quantitation, reveals some physical properties of the matrix components and goes some way to explain the common macro-scale morphologies of these structures described previously.
Supervisor: Stanley-Wall, Nicola ; Swedlow, Jason Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available
Keywords: Bacterial differentiation ; bacterial multicellularity ; biofilms ; microscopy