This research investigated the use of carbon nanotubes (CNTs) as a treatment to increase the permeability of a bacterial cell wall. Recombinant Escherichia coli BL21 (DE3) containing a plasmid that expressed Green Fluorescent Protein (GFP) and -lactamase were exposed to CNTs under various levels of agitation for different times. Fluorescence assay for GFP, optical absorbance for -lactamase activity, and Transmission Electron Microscopy (TEM) were used to determine the amount of released protein, and visually examine the permeability enhancement of the cells, respectively. It was found that more -lactamase was present in the culture fluid after treatment with CNTs in a dose dependent manner. Indeed, CNTs can lyse the cells up to 90% of maximum when compared to lysozyme treatment. Based on TEM, it is believed that this treatment damaged the cell walls to make E. coli permeable, causing periplasm proteins and enzymes to leak out into the medium. Consequently, CNTs can be used as lysis agents when it is undesirable to add an additional enzyme (lysozyme) to cause the release of intracellular proteins.
","abstract_html":"<p>This research investigated the use of carbon nanotubes (CNTs) as a treatment to increase the permeability of a bacterial cell wall. Recombinant Escherichia coli BL21 (DE3) containing a plasmid that expressed Green Fluorescent Protein (GFP) and -lactamase were exposed to CNTs under various levels of agitation for different times. Fluorescence assay for GFP, optical absorbance for -lactamase activity, and Transmission Electron Microscopy (TEM) were used to determine the amount of released protein, and visually examine the permeability enhancement of the cells, respectively. It was found that more -lactamase was present in the culture fluid after treatment with CNTs in a dose dependent manner. Indeed, CNTs can lyse the cells up to 90% of maximum when compared to lysozyme treatment. Based on TEM, it is believed that this treatment damaged the cell walls to make E. coli permeable, causing periplasm proteins and enzymes to leak out into the medium. Consequently, CNTs can be used as lysis agents when it is undesirable to add an additional enzyme (lysozyme) to cause the release of intracellular proteins.</p>","abstract_has_math":false,"creators":["Mosleh, Abdollah"],"institution":null,"degree_name":"Master of Science in Microelectronics-Photonics (MS)","degree_level":"Thesis","degree_discipline":null,"degree_department":null,"school":null,"contributors":["Kim, Jin-Woo","Henry, Ralph L."],"advisors":["Beitle, Robert R. Jr."],"committee_chairs":[],"committee_members":[],"year":2016,"date_issued":"2016-08-01T07:00:00Z","date_published":"2016-08-01T07:00:00Z","updated_at":"2026-07-24T00:59:08Z","subjects":["Applied sciences","Carbon nanotubes","Cell wall permeability","Escherichia coli","Membrane damage","Bacterial Infections and Mycoses","Biomedical","Nanotechnology Fabrication","Preventive Medicine"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://scholarworks.uark.edu/etd/1689","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Kim, Jin-Woo","Henry, Ralph L."]},{"key":"dc:contributor.advisor","label":"Advisor","values":["Beitle, Robert R. Jr."]},{"key":"dc:creator","label":"Author","values":["Mosleh, Abdollah"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2016"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2017-09-29T07:00:00Z"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Thesis"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science in Microelectronics-Photonics (MS)"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Applied sciences","Carbon nanotubes","Cell wall permeability","Escherichia coli","Membrane damage","Bacterial Infections and Mycoses","Biomedical","Nanotechnology Fabrication","Preventive Medicine"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://scholarworks.uark.edu/etd/1689"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["This research investigated the use of carbon nanotubes (CNTs) as a treatment to increase the permeability of a bacterial cell wall. Recombinant Escherichia coli BL21 (DE3) containing a plasmid that expressed Green Fluorescent Protein (GFP) and -lactamase were exposed to CNTs under various levels of agitation for different times. Fluorescence assay for GFP, optical absorbance for -lactamase activity, and Transmission Electron Microscopy (TEM) were used to determine the amount of released protein, and visually examine the permeability enhancement of the cells, respectively. It was found that more -lactamase was present in the culture fluid after treatment with CNTs in a dose dependent manner. Indeed, CNTs can lyse the cells up to 90% of maximum when compared to lysozyme treatment. Based on TEM, it is believed that this treatment damaged the cell walls to make E. coli permeable, causing periplasm proteins and enzymes to leak out into the medium. Consequently, CNTs can be used as lysis agents when it is undesirable to add an additional enzyme (lysozyme) to cause the release of intracellular proteins.
"]},{"key":"dc:title","label":"Title","values":["Investigation of CNT-induced Escherichia coli Lysis and Protein Release"]}]}],"canonical_facts":{"dc:contributor":["Kim, Jin-Woo","Henry, Ralph L."],"dc:contributor.advisor":["Beitle, Robert R. Jr."],"dc:creator":["Mosleh, Abdollah"],"dc:date":["2016"],"dc:date.available":["2017-09-29T07:00:00Z"],"dc:description.abstract":["This research investigated the use of carbon nanotubes (CNTs) as a treatment to increase the permeability of a bacterial cell wall. Recombinant Escherichia coli BL21 (DE3) containing a plasmid that expressed Green Fluorescent Protein (GFP) and -lactamase were exposed to CNTs under various levels of agitation for different times. Fluorescence assay for GFP, optical absorbance for -lactamase activity, and Transmission Electron Microscopy (TEM) were used to determine the amount of released protein, and visually examine the permeability enhancement of the cells, respectively. It was found that more -lactamase was present in the culture fluid after treatment with CNTs in a dose dependent manner. Indeed, CNTs can lyse the cells up to 90% of maximum when compared to lysozyme treatment. Based on TEM, it is believed that this treatment damaged the cell walls to make E. coli permeable, causing periplasm proteins and enzymes to leak out into the medium. Consequently, CNTs can be used as lysis agents when it is undesirable to add an additional enzyme (lysozyme) to cause the release of intracellular proteins.
"],"dc:identifier":["https://scholarworks.uark.edu/etd/1689"],"dc:subject":["Applied sciences","Carbon nanotubes","Cell wall permeability","Escherichia coli","Membrane damage","Bacterial Infections and Mycoses","Biomedical","Nanotechnology Fabrication","Preventive Medicine"],"dc:title":["Investigation of CNT-induced Escherichia coli Lysis and Protein Release"],"thesis:degree_level":["Thesis"],"thesis:degree_name":["Master of Science in Microelectronics-Photonics (MS)"]},"updated_at":"2026-07-24T00:59:08Z"}