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dc.contributor.authorAuthier, Astrid
dc.date.accessioned2017-02-15T20:48:25Z
dc.date.available2017-02-15T20:48:25Z
dc.date.issued2003
dc.identifier.urihttp://hdl.handle.net/10179/10433
dc.description.abstractThis study focuses on Lactobacillus rhamnosus HN001, a potential candidate for use as a probiotic. Probiotics are microorganisms that can exert a beneficial effect on a host. It is believed that the ability of a probiotic to colonise gastrointestinal surfaces is important in its ability to exert a beneficial effect on the host. In order to do so, it is thought the microorganism must be able to adhere to molecules found on intestinal cells. HN001 has been shown to adhere to human intestinal cell lines (Gopal et al., 2001). This study characterises the molecular species involved in the adherence of HN001 to intestinal molecules and cell lines, which may be important in the ability of HN001 to exert health benefits in a host. Both liquid and solid-phase binding assays were used to characterise HN001 binding to extracellular matrix (ECM) components found in intestinal tissues. Of the ECM components investigated, HN001 bound fibronectin with the highest affinity. This interaction was specific, saturable and dependent on the growth phase of HN001. HN001 bound immobilised fibronectin in preference to soluble fibronectin through a protein-dependent interaction. HN001 was also found to bind to the N-terminal heparin binding domain of fibronectin and the C-terminal part of the first type III repeat in the fibronectin molecule (III1-C). HN001 adhered to the human intestinal cell line, Caco-2, in a dose-dependent manner that was enhanced by a pH-sensitivc factor present in the spent culture supernatant. Since fibronectin-binding was identified as a possible mechanism for adherence of HN001 to intestinal tissues, HN001 genome DNA sequence was examined for genes encoding putative fibronectin-binding proteins. Fbl (Fibronectin-binding like) was identified through its similarity to fibronectin-binding proteins from Streptococcus pneumoniae (Holmes et al., 2001) and S. pyogenes (Courtney et al., 1994). Fbl was expressed by a GST fusion system and used to compete with HN001 adhesion in liquid-phase binding assays to ascertain its function. Since difficulties were experienced when expressing and purifying soluble Fbl, an insertional disruption of the fbl gene was created and its phenotype investigated in liquid-phase, solid-phase and Caco-2 binding assays to determine Fbl function.en_US
dc.language.isoenen_US
dc.publisherMassey Universityen_US
dc.rightsThe Authoren_US
dc.subjectLactobacillus -- Geneticsen_US
dc.titleCharacterisation of adhesion of a probiotic bacterium Lactobacillus rhamnosus HN001 to extracellular matrix proteins and the intestinal cell line Caco-2 : a thesis presented to Massey University in partial fulfilment of the requirement for the degree of Master of Science in Microbiologyen_US
dc.typeThesisen_US
thesis.degree.disciplineMicrobiologyen_US
thesis.degree.grantorMassey Universityen_US
thesis.degree.levelMastersen_US
thesis.degree.nameMaster of Science (M. Sc.)en_US


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