Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.481361
Title: Studies on the delta haemolysin of Staphylococcus aureus
Author: Smith, Gillian Margaret
ISNI:       0000 0001 3435 8500
Awarding Body: University of Leicester
Current Institution: University of Leicester
Date of Award: 1982
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Abstract:
The production of haemolysins by several strains of Staphylococcus aureus was investigated and strain RN25 chosen for further study. Three methods for the purification of delta haemolysin were compared for efficiency and purity of the products. The products were characterised using polyacrylamide gel electrophoresis, amino acid analysis and K-terminal sequence analysis. The method of Heatley (1971 and 1976) was found to be the most efficient and yielded the product of highest purity and specific activity. Prom polyacrylamide gel electrophoresis in the presence of SDS the miolecular weight of delta haemiolysin was estimated to be less than 5 000. N-terminal sequence analysis of the products of the purification procedures led to the observation that the preparations of delta haemiolysin contained a proportion of N-terminally blocked protein. Thin layer chromatography of the products revealed the three preparations of delta haemolysin to be heterogeneous. The toxin was further purified using hydrophobic affinity chromatography. The molecular weight of native delta haemolysin was estimated from gel filtration to be 150 000. The effect of chemical modification of delta haemiolysin on its haemolytic activity indicated that the N-terminus of the toxin is involved in its mechanismi of action and that the amino groups of the molecule are very important for its activity. The results were closely comparable to those observed for melittin of bee venom. Inhibitors of extracellular protein production, procaine and cerulenin, were found to inhibit the production of delta haemolysin and total extracellular protein. Using cerulenin and harvesting cultures of strain RN25 in the mid-exponential phase of growth, the possibility of the existence of a precursor of delta haemolysin was investigated using techniques of immunoprecipitation.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.481361  DOI: Not available
Keywords: Microbiology
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