{"id":{"repo_id":"mo-state","oai_identifier":"oai:bearworks.missouristate.edu:theses-2337"},"canonical_url":"https://search.dev.ndltd.org/etd/mo-state/oai:bearworks.missouristate.edu:theses-2337","repository":{"repo_id":"mo-state","name":"Missouri State University","base_url":"https://bearworks.missouristate.edu/do/oai/"},"display":{"title":"The Development of Genetic Tools for Protein Characterization and Genetic Engineering in the Acetic Acid Bacterium Gluconobacter Oxydans","abstract":"The acetic acid bacterium Gluconobacter oxydans is well known for its ability to incompletely oxidize carbon substrates under normal conditions. The incomplete oxidations are carried out by membrane-bound dehydrogenases that channel electrons directly into the electron transport chain. Many of these oxidative products are regio- and stereo-specific, and the use of G. oxydans in industrial practices allows the production of enantiopure products that can be difficult or impossible to obtain using traditional chemical synthesis. Thus, this organism is of industrial use and the improvement of strains via genetic engineering has the potential to produce novel products as well as increase the yields. However, genetic manipulation in G. oxydans is often difficult and time-consuming because few genetic tools are available for use in this organism. To this end, a series of tools have been constructed: a fluorescent-protein based screening system, a surface display system, and an inducible promoter system. The results of the construction of these three tools for use in G. oxydans and initial analyses of the effectiveness within the host are presented.","abstract_html":"The acetic acid bacterium Gluconobacter oxydans is well known for its ability to incompletely oxidize carbon substrates under normal conditions. The incomplete oxidations are carried out by membrane-bound dehydrogenases that channel electrons directly into the electron transport chain. Many of these oxidative products are regio- and stereo-specific, and the use of G. oxydans in industrial practices allows the production of enantiopure products that can be difficult or impossible to obtain using traditional chemical synthesis. Thus, this organism is of industrial use and the improvement of strains via genetic engineering has the potential to produce novel products as well as increase the yields. However, genetic manipulation in G. oxydans is often difficult and time-consuming because few genetic tools are available for use in this organism. To this end, a series of tools have been constructed: a fluorescent-protein based screening system, a surface display system, and an inducible promoter system. The results of the construction of these three tools for use in G. oxydans and initial analyses of the effectiveness within the host are presented.","abstract_has_math":false,"creators":["Pearson, Kaleb Scott"],"institution":null,"degree_name":"Master of Science in Biology","degree_level":"Masters","degree_discipline":"Biology","degree_department":null,"school":null,"contributors":["Paul Schweiger"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2014,"date_issued":"2014-12-01T08:00:00Z","date_published":"2014-12-01T08:00:00Z","updated_at":"2026-07-24T03:16:23Z","subjects":["Gluconobacter oxydans","incomplete oxidation","fluorescent reporter","surface display","inducible promoter","Biology"],"languages":[],"rights":["© Kaleb Scott Pearson"],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://bearworks.missouristate.edu/theses/1336","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Paul Schweiger"]},{"key":"dc:creator","label":"Author","values":["Pearson, Kaleb Scott"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"thesis:degree_discipline","label":"Discipline","values":["Biology"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Masters"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science in Biology"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Gluconobacter oxydans","incomplete oxidation","fluorescent reporter","surface display","inducible promoter","Biology"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:rights","label":"Dc Rights","values":["© Kaleb Scott Pearson"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://bearworks.missouristate.edu/theses/1336"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["The acetic acid bacterium Gluconobacter oxydans is well known for its ability to incompletely oxidize carbon substrates under normal conditions. The incomplete oxidations are carried out by membrane-bound dehydrogenases that channel electrons directly into the electron transport chain. Many of these oxidative products are regio- and stereo-specific, and the use of G. oxydans in industrial practices allows the production of enantiopure products that can be difficult or impossible to obtain using traditional chemical synthesis. Thus, this organism is of industrial use and the improvement of strains via genetic engineering has the potential to produce novel products as well as increase the yields. However, genetic manipulation in G. oxydans is often difficult and time-consuming because few genetic tools are available for use in this organism. To this end, a series of tools have been constructed: a fluorescent-protein based screening system, a surface display system, and an inducible promoter system. The results of the construction of these three tools for use in G. oxydans and initial analyses of the effectiveness within the host are presented."]},{"key":"dc:title","label":"Title","values":["The Development of Genetic Tools for Protein Characterization and Genetic Engineering in the Acetic Acid Bacterium Gluconobacter Oxydans"]}]}],"canonical_facts":{"dc:contributor":["Paul Schweiger"],"dc:creator":["Pearson, Kaleb Scott"],"dc:description.abstract":["The acetic acid bacterium Gluconobacter oxydans is well known for its ability to incompletely oxidize carbon substrates under normal conditions. The incomplete oxidations are carried out by membrane-bound dehydrogenases that channel electrons directly into the electron transport chain. Many of these oxidative products are regio- and stereo-specific, and the use of G. oxydans in industrial practices allows the production of enantiopure products that can be difficult or impossible to obtain using traditional chemical synthesis. Thus, this organism is of industrial use and the improvement of strains via genetic engineering has the potential to produce novel products as well as increase the yields. However, genetic manipulation in G. oxydans is often difficult and time-consuming because few genetic tools are available for use in this organism. To this end, a series of tools have been constructed: a fluorescent-protein based screening system, a surface display system, and an inducible promoter system. The results of the construction of these three tools for use in G. oxydans and initial analyses of the effectiveness within the host are presented."],"dc:identifier":["https://bearworks.missouristate.edu/theses/1336"],"dc:rights":["© Kaleb Scott Pearson"],"dc:subject":["Gluconobacter oxydans","incomplete oxidation","fluorescent reporter","surface display","inducible promoter","Biology"],"dc:title":["The Development of Genetic Tools for Protein Characterization and Genetic Engineering in the Acetic Acid Bacterium Gluconobacter Oxydans"],"thesis:degree_discipline":["Biology"],"thesis:degree_level":["Masters"],"thesis:degree_name":["Master of Science in Biology"]},"updated_at":"2026-07-24T03:16:23Z"}