{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/26268"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/26268","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Construction of green fluorescent protein plasmids for labeling of herbicide-degrading Delftia acidovorans MC1071","abstract":"Each year, approximately 46 million pounds of 2,4-dichlorophenoxyacetate (2,4-D) (EPA, 2005) and 4 million pounds of 2,4-dichlorophenoxypropionate (2,4-DP) (EPA, 2007) herbicides are applied for commercial or residential usage in the US. Accidental runoff of herbicides such as 2,4-D and 2,4-DP from human applications is toxic to non-target organisms and harmful to the environment. The main mode of removal for most herbicides in nature is biodegradation. In natural environments, herbicides and substrates are non-uniformly distributed, and microorganisms compete to degrade these compounds. The favorability of one microbe over another depends on many factors, including the herbicide and substrate concentrations. The objective of my research is to construct two green-fluorescent protein (GFP) plasmids to tag a specific strain of D. acidovorans (MC1071) for visual distinction from one or more competing microbes in a microfluidic pore structure that contains spatially varying concentrations of 2,4-DP, 2,4-D, and/or oxygen. Two GFP plasmids, designated pKNlacgfp and pKNtfdgfp, were constructed and successfully transformed into MC1071. One resultant strain, MC1071/pKNlacgfp, constitutively expressed GFP, while the strain MC1071/pKNtfdgfp expressed GFP only when herbicide degradation was induced. The MC1071/pKNlacgfp strain will now be visually distinct from other D. acidovorans strains when grown in micromodels, allowing for monitoring of competition between MC1071 and other strains. The MC1071/pKNtfdgfp strain will allow distinction of active and inactive MC1071 biomass in micromodels, thus facilitating the study of bacteria adaptation in micromodels.","abstract_html":"Each year, approximately 46 million pounds of 2,4-dichlorophenoxyacetate (2,4-D) (EPA, 2005) and 4 million pounds of 2,4-dichlorophenoxypropionate (2,4-DP) (EPA, 2007) herbicides are applied for commercial or residential usage in the US. Accidental runoff of herbicides such as 2,4-D and 2,4-DP from human applications is toxic to non-target organisms and harmful to the environment. The main mode of removal for most herbicides in nature is biodegradation. In natural environments, herbicides and substrates are non-uniformly distributed, and microorganisms compete to degrade these compounds. The favorability of one microbe over another depends on many factors, including the herbicide and substrate concentrations. The objective of my research is to construct two green-fluorescent protein (GFP) plasmids to tag a specific strain of D. acidovorans (MC1071) for visual distinction from one or more competing microbes in a microfluidic pore structure that contains spatially varying concentrations of 2,4-DP, 2,4-D, and/or oxygen. Two GFP plasmids, designated pKNlacgfp and pKNtfdgfp, were constructed and successfully transformed into MC1071. One resultant strain, MC1071/pKNlacgfp, constitutively expressed GFP, while the strain MC1071/pKNtfdgfp expressed GFP only when herbicide degradation was induced. The MC1071/pKNlacgfp strain will now be visually distinct from other D. acidovorans strains when grown in micromodels, allowing for monitoring of competition between MC1071 and other strains. The MC1071/pKNtfdgfp strain will allow distinction of active and inactive MC1071 biomass in micromodels, thus facilitating the study of bacteria adaptation in micromodels.","abstract_has_math":false,"creators":["Ng, Kenneth Siu Hin"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"M.S.","degree_level":"Thesis","degree_discipline":"Environ Engr in Civil Engr","degree_department":null,"school":null,"contributors":["Werth, Charles J.","Zilles, Julie L."],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2011,"date_issued":"2011-08-25T22:21:31Z","date_published":"2011-08-25T22:21:31Z","updated_at":"2026-07-22T22:25:26Z","subjects":["Green Fluorescent Protein (GFP)","Delftia acidovorans","2,4-Dichlorophenoxyacetic Acid","2,4-Dichlorophenoxypropanoic Acid","tfdC Promoter","Micromodels","Herbicide Degradation"],"languages":["en"],"rights":["Copyright 2011 Kenneth Siu Hin Ng"],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/2142/26268","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Werth, Charles J.","Zilles, Julie L."]},{"key":"dc:creator","label":"Author","values":["Ng, Kenneth Siu Hin"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2011-08-25T22:21:31Z","2011-08"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Environ Engr in Civil Engr"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Thesis"]},{"key":"thesis:degree_name","label":"Degree Name","values":["M.S."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Illinois at Urbana-Champaign"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Green Fluorescent Protein (GFP)","Delftia acidovorans","2,4-Dichlorophenoxyacetic Acid","2,4-Dichlorophenoxypropanoic Acid","tfdC Promoter","Micromodels","Herbicide Degradation"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["en"]},{"key":"dc:rights","label":"Dc Rights","values":["Copyright 2011 Kenneth Siu Hin Ng"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["http://hdl.handle.net/2142/26268"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Each year, approximately 46 million pounds of 2,4-dichlorophenoxyacetate (2,4-D) (EPA, 2005) and 4 million pounds of 2,4-dichlorophenoxypropionate (2,4-DP) (EPA, 2007) herbicides are applied for commercial or residential usage in the US. Accidental runoff of herbicides such as 2,4-D and 2,4-DP from human applications is toxic to non-target organisms and harmful to the environment. The main mode of removal for most herbicides in nature is biodegradation. In natural environments, herbicides and substrates are non-uniformly distributed, and microorganisms compete to degrade these compounds. The favorability of one microbe over another depends on many factors, including the herbicide and substrate concentrations. The objective of my research is to construct two green-fluorescent protein (GFP) plasmids to tag a specific strain of D. acidovorans (MC1071) for visual distinction from one or more competing microbes in a microfluidic pore structure that contains spatially varying concentrations of 2,4-DP, 2,4-D, and/or oxygen. Two GFP plasmids, designated pKNlacgfp and pKNtfdgfp, were constructed and successfully transformed into MC1071. One resultant strain, MC1071/pKNlacgfp, constitutively expressed GFP, while the strain MC1071/pKNtfdgfp expressed GFP only when herbicide degradation was induced. The MC1071/pKNlacgfp strain will now be visually distinct from other D. acidovorans strains when grown in micromodels, allowing for monitoring of competition between MC1071 and other strains. The MC1071/pKNtfdgfp strain will allow distinction of active and inactive MC1071 biomass in micromodels, thus facilitating the study of bacteria adaptation in micromodels.","Item withdrawn by Mark Zulauf (zulauf@illinois.edu) on 2011-07-22T12:23:29Z Item was in collections: University of Illinois Theses & Dissertations (ID: 1) No. of bitstreams: 2 Ng_KennethSiuHin.docx: 1627774 bytes, checksum: 8febd246de224ed21d7b0dae10fef0e6 (MD5) Ng_KennethSiuHin.pdf: 1163957 bytes, checksum: e9d093a76eb97b51c69ae2d81e92a59f (MD5)","Made available in DSpace on 2011-08-25T22:21:31Z (GMT). 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The main mode of removal for most herbicides in nature is biodegradation. In natural environments, herbicides and substrates are non-uniformly distributed, and microorganisms compete to degrade these compounds. The favorability of one microbe over another depends on many factors, including the herbicide and substrate concentrations. The objective of my research is to construct two green-fluorescent protein (GFP) plasmids to tag a specific strain of D. acidovorans (MC1071) for visual distinction from one or more competing microbes in a microfluidic pore structure that contains spatially varying concentrations of 2,4-DP, 2,4-D, and/or oxygen. Two GFP plasmids, designated pKNlacgfp and pKNtfdgfp, were constructed and successfully transformed into MC1071. One resultant strain, MC1071/pKNlacgfp, constitutively expressed GFP, while the strain MC1071/pKNtfdgfp expressed GFP only when herbicide degradation was induced. The MC1071/pKNlacgfp strain will now be visually distinct from other D. acidovorans strains when grown in micromodels, allowing for monitoring of competition between MC1071 and other strains. The MC1071/pKNtfdgfp strain will allow distinction of active and inactive MC1071 biomass in micromodels, thus facilitating the study of bacteria adaptation in micromodels.","Item withdrawn by Mark Zulauf (zulauf@illinois.edu) on 2011-07-22T12:23:29Z Item was in collections: University of Illinois Theses & Dissertations (ID: 1) No. of bitstreams: 2 Ng_KennethSiuHin.docx: 1627774 bytes, checksum: 8febd246de224ed21d7b0dae10fef0e6 (MD5) Ng_KennethSiuHin.pdf: 1163957 bytes, checksum: e9d093a76eb97b51c69ae2d81e92a59f (MD5)","Made available in DSpace on 2011-08-25T22:21:31Z (GMT). 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