{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/88252"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/88252","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"The iron-dependent cyanide and hydrogen peroxide co-toxicity in Escherichia coli and its catastrophic consequences for the chromosome","abstract":"Hydrogen peroxide (H2O2) can oxidize cytoplasmic ferrous ions (Fe2+) to produce highly reactive hydroxyl radicals (•OH) via Fenton’s reaction that can damage various biomolecules causing oxidative stress. Even though at concentrations higher than 20 mM H2O2 by itself can efficiently kill micro-organisms, it is metabolically impossible for eukaryotic cells to generate H2O2, an uncharged molecule, in such large quantities inside the cell. We propose that potentiation of physiologically relevant amounts of H2O2 by various small molecules serves as a more feasible and safe mechanism to combat invading microbes. NO potentiation of H2O2 toxicity is a known bactericidal weapon employed by macrophages. In fact, in human neutrophils activated by bacterial infection, the myeloperoxidase enzyme catalyzes the formation of hydrogen cyanide (HCN) from serum thiocyanate (SCN-). In the past, researchers have reported that a combination of low millimolar doses of H2O2 and cyanide (CN), which are individually bacteriostatic, caused rapid synergistic killing in Escherichia coli. Our aim is to understand the immune cells antimicrobial responses by investigating the mechanism of CN potentiation of H2O2 toxicity and its chromosomal consequences. We have found that the ability of CN to recruit iron from intracellular depots such as ferritin contributes to its potentiation of H2O2 toxicity, whereas the major stationary phase intracellular iron depot protein, Dps, can sequester this iron, thereby quelling Fenton's reaction. Our work has also demonstrated that this synergistic toxicity is associated with catastrophic chromosomal fragmentation, which is blocked by iron chelators. Moreover, the CN + H2O2 treatment also resulted in destruction of ribosomal RNA, indicating that RNA is equally susceptible to the oxidative damage induced. The catastrophic chromosomal fragmentation induced by CN and H2O2 was found to be cell density-dependent, but replication- and translation-independent. We propose that disrupting intracellular iron trafficking to cause catastrophic chromosomal fragmentation is a common strategy employed by the immune system to kill invading microbes. We also showed that the base excision repair pathway plays the major role in preventing this catastrophic chromosomal fragmentation, which indicates that the double-strand breaks induced by CN + H2O2 are preceded by a significant number of base modifications, removed by base-excision repair via the abasic site intermediates. These lesions can be converted into double-strand breaks that are repairable via the recombinational repair system. On the other hand, termination of the CN + H2O2 treatment, which results in termination of the CN-induced block of respiration and ATP production, was found to trigger significant linear DNA degradation and disintegration of the nucleoid structure. We have shown that this disassembly of the nucleoid structure following the removal of CN and H2O2 is affected by the nucleoid-associated proteins and depends on ongoing transcription, thereby revealing the role of transcription in the nucleoid dynamics. Therefore, we conclude that cyanide potentiates hydrogen peroxide toxicity by recruiting iron from intracellular depots directly onto the DNA, where the DNA-iron complexes catalyze self-targeted Fenton's reaction leading to catastrophic DNA damage. This massive DNA damage is actively countered by base-excision repair mechanisms, but it eventually saturates the cellular DNA repair capacity and causes disintegration of the trancriptionally-active nucleoids.","abstract_html":"Hydrogen peroxide (H2O2) can oxidize cytoplasmic ferrous ions (Fe2+) to produce highly reactive hydroxyl radicals (•OH) via Fenton’s reaction that can damage various biomolecules causing oxidative stress. Even though at concentrations higher than 20 mM H2O2 by itself can efficiently kill micro-organisms, it is metabolically impossible for eukaryotic cells to generate H2O2, an uncharged molecule, in such large quantities inside the cell. We propose that potentiation of physiologically relevant amounts of H2O2 by various small molecules serves as a more feasible and safe mechanism to combat invading microbes. NO potentiation of H2O2 toxicity is a known bactericidal weapon employed by macrophages. In fact, in human neutrophils activated by bacterial infection, the myeloperoxidase enzyme catalyzes the formation of hydrogen cyanide (HCN) from serum thiocyanate (SCN-). In the past, researchers have reported that a combination of low millimolar doses of H2O2 and cyanide (CN), which are individually bacteriostatic, caused rapid synergistic killing in Escherichia coli. Our aim is to understand the immune cells antimicrobial responses by investigating the mechanism of CN potentiation of H2O2 toxicity and its chromosomal consequences. We have found that the ability of CN to recruit iron from intracellular depots such as ferritin contributes to its potentiation of H2O2 toxicity, whereas the major stationary phase intracellular iron depot protein, Dps, can sequester this iron, thereby quelling Fenton's reaction. Our work has also demonstrated that this synergistic toxicity is associated with catastrophic chromosomal fragmentation, which is blocked by iron chelators. Moreover, the CN + H2O2 treatment also resulted in destruction of ribosomal RNA, indicating that RNA is equally susceptible to the oxidative damage induced. The catastrophic chromosomal fragmentation induced by CN and H2O2 was found to be cell density-dependent, but replication- and translation-independent. We propose that disrupting intracellular iron trafficking to cause catastrophic chromosomal fragmentation is a common strategy employed by the immune system to kill invading microbes. We also showed that the base excision repair pathway plays the major role in preventing this catastrophic chromosomal fragmentation, which indicates that the double-strand breaks induced by CN + H2O2 are preceded by a significant number of base modifications, removed by base-excision repair via the abasic site intermediates. These lesions can be converted into double-strand breaks that are repairable via the recombinational repair system. On the other hand, termination of the CN + H2O2 treatment, which results in termination of the CN-induced block of respiration and ATP production, was found to trigger significant linear DNA degradation and disintegration of the nucleoid structure. We have shown that this disassembly of the nucleoid structure following the removal of CN and H2O2 is affected by the nucleoid-associated proteins and depends on ongoing transcription, thereby revealing the role of transcription in the nucleoid dynamics. Therefore, we conclude that cyanide potentiates hydrogen peroxide toxicity by recruiting iron from intracellular depots directly onto the DNA, where the DNA-iron complexes catalyze self-targeted Fenton's reaction leading to catastrophic DNA damage. This massive DNA damage is actively countered by base-excision repair mechanisms, but it eventually saturates the cellular DNA repair capacity and causes disintegration of the trancriptionally-active nucleoids.","abstract_has_math":false,"creators":["Mahaseth, Tulip"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Microbiology","degree_department":null,"school":null,"contributors":["Kuzminov, Andrei","Cronan, John E.","Gardner, Jeffrey F.","Vanderpool, Carin K."],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2015,"date_issued":"2015-09-29T21:02:52Z","date_published":"2015-09-29T21:02:52Z","updated_at":"2026-07-22T22:26:31Z","subjects":["cyanide","potentiated hydrogen peroxide toxicity","catastrophic chromosomal fragmentation","iron metabolism","Fenton's reaction","immune system's anti-microbial mechanisms","nucleoid dynamics"],"languages":["en"],"rights":["Copyright 2015 Tulip Mahaseth"],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/2142/88252","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Kuzminov, Andrei","Cronan, John E.","Gardner, Jeffrey F.","Vanderpool, Carin K."]},{"key":"dc:creator","label":"Author","values":["Mahaseth, Tulip"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2015-09-29T21:02:52Z","2017-09-30T09:15:30Z","2015-08","2015-06-22","2015-8"]},{"key":"dc:type","label":"Dc Type","values":["text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Microbiology"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Ph.D."]},{"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":["cyanide","potentiated hydrogen peroxide toxicity","catastrophic chromosomal fragmentation","iron metabolism","Fenton's reaction","immune system's anti-microbial mechanisms","nucleoid dynamics"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["en"]},{"key":"dc:rights","label":"Dc Rights","values":["Copyright 2015 Tulip Mahaseth"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["http://hdl.handle.net/2142/88252"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Hydrogen peroxide (H2O2) can oxidize cytoplasmic ferrous ions (Fe2+) to produce highly reactive hydroxyl radicals (•OH) via Fenton’s reaction that can damage various biomolecules causing oxidative stress. Even though at concentrations higher than 20 mM H2O2 by itself can efficiently kill micro-organisms, it is metabolically impossible for eukaryotic cells to generate H2O2, an uncharged molecule, in such large quantities inside the cell. We propose that potentiation of physiologically relevant amounts of H2O2 by various small molecules serves as a more feasible and safe mechanism to combat invading microbes. NO potentiation of H2O2 toxicity is a known bactericidal weapon employed by macrophages. In fact, in human neutrophils activated by bacterial infection, the myeloperoxidase enzyme catalyzes the formation of hydrogen cyanide (HCN) from serum thiocyanate (SCN-). In the past, researchers have reported that a combination of low millimolar doses of H2O2 and cyanide (CN), which are individually bacteriostatic, caused rapid synergistic killing in Escherichia coli. Our aim is to understand the immune cells antimicrobial responses by investigating the mechanism of CN potentiation of H2O2 toxicity and its chromosomal consequences. We have found that the ability of CN to recruit iron from intracellular depots such as ferritin contributes to its potentiation of H2O2 toxicity, whereas the major stationary phase intracellular iron depot protein, Dps, can sequester this iron, thereby quelling Fenton's reaction. Our work has also demonstrated that this synergistic toxicity is associated with catastrophic chromosomal fragmentation, which is blocked by iron chelators. Moreover, the CN + H2O2 treatment also resulted in destruction of ribosomal RNA, indicating that RNA is equally susceptible to the oxidative damage induced. The catastrophic chromosomal fragmentation induced by CN and H2O2 was found to be cell density-dependent, but replication- and translation-independent. We propose that disrupting intracellular iron trafficking to cause catastrophic chromosomal fragmentation is a common strategy employed by the immune system to kill invading microbes. We also showed that the base excision repair pathway plays the major role in preventing this catastrophic chromosomal fragmentation, which indicates that the double-strand breaks induced by CN + H2O2 are preceded by a significant number of base modifications, removed by base-excision repair via the abasic site intermediates. These lesions can be converted into double-strand breaks that are repairable via the recombinational repair system. On the other hand, termination of the CN + H2O2 treatment, which results in termination of the CN-induced block of respiration and ATP production, was found to trigger significant linear DNA degradation and disintegration of the nucleoid structure. We have shown that this disassembly of the nucleoid structure following the removal of CN and H2O2 is affected by the nucleoid-associated proteins and depends on ongoing transcription, thereby revealing the role of transcription in the nucleoid dynamics. Therefore, we conclude that cyanide potentiates hydrogen peroxide toxicity by recruiting iron from intracellular depots directly onto the DNA, where the DNA-iron complexes catalyze self-targeted Fenton's reaction leading to catastrophic DNA damage. This massive DNA damage is actively countered by base-excision repair mechanisms, but it eventually saturates the cellular DNA repair capacity and causes disintegration of the trancriptionally-active nucleoids.","Submission published under a 24 month embargo labeled 'Closed Access', the embargo will last until 2017-08-01","The student, Tulip Mahaseth, accepted the attached license on 2015-06-19 at 09:04.","The student, Tulip Mahaseth, submitted this Dissertation for approval on 2015-06-19 at 09:23.","This Dissertation was approved for publication on 2015-06-22 at 08:16.","DSpace SAF Submission Ingestion Package generated from Vireo submission #8296 on 2015-09-29 at 15:05:16","Made available in DSpace on 2015-09-29T21:02:52Z (GMT). No. of bitstreams: 2 MAHASETH-DISSERTATION-2015.pdf: 6081154 bytes, checksum: 174624b4b82e8be4c15701cf529afcdb (MD5) LICENSE.txt: 4211 bytes, checksum: 9105235d1a802799aa12f26942ebca5f (MD5) Previous issue date: 2015-06-22","Embargo set by: Seth Robbins for item 89532 Lift date: 2017-09-29T21:03:28Z Reason: Author requested closed access (OA after 2yrs) in Vireo ETD system","Embargo set by: Seth Robbins for item 89532 Lift date: 2017-09-29T21:08:35Z Reason: Author requested closed access (OA after 2yrs) in Vireo ETD system","Limited Restriction Lifted for Item 89532 on 2017-09-30T09:15:30Z."]},{"key":"dc:format","label":"Dc Format","values":["application/pdf"]},{"key":"dc:title","label":"Title","values":["The iron-dependent cyanide and hydrogen peroxide co-toxicity in Escherichia coli and its catastrophic consequences for the chromosome"]}]}],"canonical_facts":{"dc:contributor":["Kuzminov, Andrei","Cronan, John E.","Gardner, Jeffrey F.","Vanderpool, Carin K."],"dc:creator":["Mahaseth, Tulip"],"dc:date":["2015-09-29T21:02:52Z","2017-09-30T09:15:30Z","2015-08","2015-06-22","2015-8"],"dc:description":["Hydrogen peroxide (H2O2) can oxidize cytoplasmic ferrous ions (Fe2+) to produce highly reactive hydroxyl radicals (•OH) via Fenton’s reaction that can damage various biomolecules causing oxidative stress. Even though at concentrations higher than 20 mM H2O2 by itself can efficiently kill micro-organisms, it is metabolically impossible for eukaryotic cells to generate H2O2, an uncharged molecule, in such large quantities inside the cell. We propose that potentiation of physiologically relevant amounts of H2O2 by various small molecules serves as a more feasible and safe mechanism to combat invading microbes. NO potentiation of H2O2 toxicity is a known bactericidal weapon employed by macrophages. In fact, in human neutrophils activated by bacterial infection, the myeloperoxidase enzyme catalyzes the formation of hydrogen cyanide (HCN) from serum thiocyanate (SCN-). In the past, researchers have reported that a combination of low millimolar doses of H2O2 and cyanide (CN), which are individually bacteriostatic, caused rapid synergistic killing in Escherichia coli. Our aim is to understand the immune cells antimicrobial responses by investigating the mechanism of CN potentiation of H2O2 toxicity and its chromosomal consequences. We have found that the ability of CN to recruit iron from intracellular depots such as ferritin contributes to its potentiation of H2O2 toxicity, whereas the major stationary phase intracellular iron depot protein, Dps, can sequester this iron, thereby quelling Fenton's reaction. Our work has also demonstrated that this synergistic toxicity is associated with catastrophic chromosomal fragmentation, which is blocked by iron chelators. Moreover, the CN + H2O2 treatment also resulted in destruction of ribosomal RNA, indicating that RNA is equally susceptible to the oxidative damage induced. The catastrophic chromosomal fragmentation induced by CN and H2O2 was found to be cell density-dependent, but replication- and translation-independent. We propose that disrupting intracellular iron trafficking to cause catastrophic chromosomal fragmentation is a common strategy employed by the immune system to kill invading microbes. We also showed that the base excision repair pathway plays the major role in preventing this catastrophic chromosomal fragmentation, which indicates that the double-strand breaks induced by CN + H2O2 are preceded by a significant number of base modifications, removed by base-excision repair via the abasic site intermediates. These lesions can be converted into double-strand breaks that are repairable via the recombinational repair system. On the other hand, termination of the CN + H2O2 treatment, which results in termination of the CN-induced block of respiration and ATP production, was found to trigger significant linear DNA degradation and disintegration of the nucleoid structure. We have shown that this disassembly of the nucleoid structure following the removal of CN and H2O2 is affected by the nucleoid-associated proteins and depends on ongoing transcription, thereby revealing the role of transcription in the nucleoid dynamics. Therefore, we conclude that cyanide potentiates hydrogen peroxide toxicity by recruiting iron from intracellular depots directly onto the DNA, where the DNA-iron complexes catalyze self-targeted Fenton's reaction leading to catastrophic DNA damage. This massive DNA damage is actively countered by base-excision repair mechanisms, but it eventually saturates the cellular DNA repair capacity and causes disintegration of the trancriptionally-active nucleoids.","Submission published under a 24 month embargo labeled 'Closed Access', the embargo will last until 2017-08-01","The student, Tulip Mahaseth, accepted the attached license on 2015-06-19 at 09:04.","The student, Tulip Mahaseth, submitted this Dissertation for approval on 2015-06-19 at 09:23.","This Dissertation was approved for publication on 2015-06-22 at 08:16.","DSpace SAF Submission Ingestion Package generated from Vireo submission #8296 on 2015-09-29 at 15:05:16","Made available in DSpace on 2015-09-29T21:02:52Z (GMT). No. of bitstreams: 2 MAHASETH-DISSERTATION-2015.pdf: 6081154 bytes, checksum: 174624b4b82e8be4c15701cf529afcdb (MD5) LICENSE.txt: 4211 bytes, checksum: 9105235d1a802799aa12f26942ebca5f (MD5) Previous issue date: 2015-06-22","Embargo set by: Seth Robbins for item 89532 Lift date: 2017-09-29T21:03:28Z Reason: Author requested closed access (OA after 2yrs) in Vireo ETD system","Embargo set by: Seth Robbins for item 89532 Lift date: 2017-09-29T21:08:35Z Reason: Author requested closed access (OA after 2yrs) in Vireo ETD system","Limited Restriction Lifted for Item 89532 on 2017-09-30T09:15:30Z."],"dc:format":["application/pdf"],"dc:identifier":["http://hdl.handle.net/2142/88252"],"dc:language":["en"],"dc:rights":["Copyright 2015 Tulip Mahaseth"],"dc:subject":["cyanide","potentiated hydrogen peroxide toxicity","catastrophic chromosomal fragmentation","iron metabolism","Fenton's reaction","immune system's anti-microbial mechanisms","nucleoid dynamics"],"dc:title":["The iron-dependent cyanide and hydrogen peroxide co-toxicity in Escherichia coli and its catastrophic consequences for the chromosome"],"dc:type":["text"],"thesis:degree_discipline":["Microbiology"],"thesis:degree_level":["Dissertation"],"thesis:degree_name":["Ph.D."],"thesis:institution_name":["University of Illinois at Urbana-Champaign"]},"updated_at":"2026-07-22T22:26:31Z"}