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Studies on the regulation of extracellular collagenase production by vibrio alginolyticus

Bibliography: leaves 117-133.

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Bibliographic Details
Main Author: Reid, Graham Charlton
Other Authors: Woods, David R
Format: Thesis
Language:English
Published: Department of Molecular and Cell Biology 2014
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access_status_str Open Access
author Reid, Graham Charlton
author2 Woods, David R
author_browse Reid, Graham Charlton
Woods, David R
author_facet Woods, David R
Reid, Graham Charlton
author_sort Reid, Graham Charlton
collection Thesis
description Bibliography: leaves 117-133.
format Thesis
id oai:open.uct.ac.za:11427/9978
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:38:45.067Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2014
publishDateRange 2014
publishDateSort 2014
publisher Department of Molecular and Cell Biology
publisherStr Department of Molecular and Cell Biology
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/9978 Studies on the regulation of extracellular collagenase production by vibrio alginolyticus Reid, Graham Charlton Woods, David R Robb, Frank T Microbiology Bibliography: leaves 117-133. Vibrio alginolyticus synthesized extracellular collagenase in a highly aerated peptone medium at the late-exponential and early-stationary phases of growth. Collagenase synthesis was subject to end-product repression and was repressed by various amino acids and ammonium ions. Glutamine caused severe repression of collagenase production. Collagenase synthesis was sensitive to catabolite repression by glucose and a number of carbon sources. Cyclic AMP, dibutyryl cyclic AMP and cyclic GMP did not relieve catabolite repression. Glucose and 2-deoxyglucose caused a severe transient repression. No intracellular preformed collagenase was detected and collagenase production ceased when induced cells were washed and resuspended in buffer.Trypsin and a-chymotrypsin had no effect on collagenase production by cells or sphaeroplasts. The inducers of collagenase production in peptone were shown to have abroad molecular weight range between 1, 000 and 60,000. The peptone inducers supported slow growth of V. alginolyticus when supplied as the sole nitrogen source in minimal medium. Digestion of the peptone inducers with purified V. alginolyticus collagenase resulted in a decrease in their inducing ability,whereas digestion with trypsin or a-chymotrypsin did not. Peptone acted as an inhibitor of collagenase. 2014-12-13T06:22:46Z 2014-12-13T06:22:46Z 1981 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/9978 eng application/pdf Department of Molecular and Cell Biology Faculty of Science University of Cape Town
spellingShingle Microbiology
Reid, Graham Charlton
Studies on the regulation of extracellular collagenase production by vibrio alginolyticus
thesis_degree_str Doctoral
title Studies on the regulation of extracellular collagenase production by vibrio alginolyticus
title_full Studies on the regulation of extracellular collagenase production by vibrio alginolyticus
title_fullStr Studies on the regulation of extracellular collagenase production by vibrio alginolyticus
title_full_unstemmed Studies on the regulation of extracellular collagenase production by vibrio alginolyticus
title_short Studies on the regulation of extracellular collagenase production by vibrio alginolyticus
title_sort studies on the regulation of extracellular collagenase production by vibrio alginolyticus
topic Microbiology
url http://hdl.handle.net/11427/9978
work_keys_str_mv AT reidgrahamcharlton studiesontheregulationofextracellularcollagenaseproductionbyvibrioalginolyticus