Nitric Oxide Generated from Isoniazid Activation by KatG: Source of Nitric Oxide and Activity against Mycobacterium tuberculosis

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Published in:Antimicrobial Agents and Chemotherapy Vol. 48; no. 8; pp. 3006 - 3009
Main Authors: TIMMINS, Graham S, MASTER, Sharon, RUSNAK, Frank, DERETIC, Vojo
Format: Journal Article
Language:English
Published: Washington, DC American Society for Microbiology 01-08-2004
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Abstract Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue AAC About AAC Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy AAC RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0066-4804 Online ISSN: 1098-6596 Copyright © 2014 by the American Society for Microbiology.   For an alternate route to AAC .asm.org, visit: AAC       
AbstractList Isonicotinic acid hydrazide (INH) is a frontline antituberculosis agent. Once taken up by Mycobacterium tuberculosis, INH requires activation by the catalase-peroxidase KatG, converting INH from its prodrug form into a range of bactericidal reactive species. Here we used 15N-labeled INH together with electron paramagnetic resonance spin trapping techniques to demonstrate that nitric oxide (NO˙) is generated from oxidation at the hydrazide nitrogens during the activation of INH by M. tuberculosis KatG. We also observed that a specific scavenger of NO˙ provided protection against the antimycobacterial activity of INH in bacterial culture. No significant increases in mycobacterial protein nitration were detected, suggesting that NO˙ and not peroxynitrite, a nitrating metabolite of NO·, is involved in antimycobacterial action. In conclusion, INH-derived NO· has biological activity, which directly contributes to the antimycobacterial action of INH.
Isonicotinic acid hydrazide (INH) is a frontline antituberculosis agent. Once taken up by Mycobacterium tuberculosis , INH requires activation by the catalase-peroxidase KatG, converting INH from its prodrug form into a range of bactericidal reactive species. Here we used 15 N-labeled INH together with electron paramagnetic resonance spin trapping techniques to demonstrate that nitric oxide (NO˙) is generated from oxidation at the hydrazide nitrogens during the activation of INH by M. tuberculosis KatG. We also observed that a specific scavenger of NO˙ provided protection against the antimycobacterial activity of INH in bacterial culture. No significant increases in mycobacterial protein nitration were detected, suggesting that NO˙ and not peroxynitrite, a nitrating metabolite of NO · , is involved in antimycobacterial action. In conclusion, INH-derived NO · has biological activity, which directly contributes to the antimycobacterial action of INH.
Isonicotinic acid hydrazide (INH) is a frontline antituberculosis agent. Once taken up by Mycobacterium tuberculosis, INH requires activation by the catalase-peroxidase KatG, converting INH from its prodrug form into a range of bactericidal reactive species. Here we used 15N-labeled INH together with electron paramagnetic resonance spin trapping techniques to demonstrate that nitric oxide (NO*) is generated from oxidation at the hydrazide nitrogens during the activation of INH by M. tuberculosis KatG. We also observed that a specific scavenger of NO* provided protection against the antimycobacterial activity of INH in bacterial culture. No significant increases in mycobacterial protein nitration were detected, suggesting that NOdot; and not peroxynitrite, a nitrating metabolite of NO*, is involved in antimycobacterial action. In conclusion, INH-derived NO* has biological activity, which directly contributes to the antimycobacterial action of INH.
Isonicotinic acid hydrazide (INH) is a frontline antituberculosis agent. Once taken up by Mycobacterium tuberculosis , INH requires activation by the catalase-peroxidase KatG, converting INH from its prodrug form into a range of bactericidal reactive species. Here we used 15 N-labeled INH together with electron paramagnetic resonance spin trapping techniques to demonstrate that nitric oxide (NȮ) is generated from oxidation at the hydrazide nitrogens during the activation of INH by M. tuberculosis KatG. We also observed that a specific scavenger of NȮ provided protection against the antimycobacterial activity of INH in bacterial culture. No significant increases in mycobacterial protein nitration were detected, suggesting that NȮ and not peroxynitrite, a nitrating metabolite of NO · , is involved in antimycobacterial action. In conclusion, INH-derived NO · has biological activity, which directly contributes to the antimycobacterial action of INH.
Isonicotinic acid hydrazide (INH) is a frontline antituberculosis agent. Once taken up by Mycobacterium tuberculosis, INH requires activation by the catalase-peroxidase KatG, converting INH from its prodrug form into a range of bactericidal reactive species. Here we used super(15)N-labeled INH together with electron paramagnetic resonance spin trapping techniques to demonstrate that nitric oxide (NO super(.)) is generated from oxidation at the hydrazide nitrogens during the activation of INH by M. tuberculosis KatG. We also observed that a specific scavenger of NO super(.) provided protection against the antimycobacterial activity of INH in bacterial culture. No significant increases in mycobacterial protein nitration were detected, suggesting that NO super(.) and not peroxynitrite, a nitrating metabolite of NO super(.), is involved in antimycobacterial action. In conclusion, INH-derived NO super(.) has biological activity, which directly contributes to the antimycobacterial action of INH.
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Author Vojo Deretic
Frank Rusnak
Sharon Master
Graham S. Timmins
AuthorAffiliation College of Pharmacy, Toxicology Program, 1 Department of Molecular Genetics and Microbiology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico 87131, 2 Department of Biochemistry and Molecular Biology and Section of Hematology Research, Mayo Clinic and Foundation, Rochester, Minnesota 55905 3
AuthorAffiliation_xml – name: College of Pharmacy, Toxicology Program, 1 Department of Molecular Genetics and Microbiology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico 87131, 2 Department of Biochemistry and Molecular Biology and Section of Hematology Research, Mayo Clinic and Foundation, Rochester, Minnesota 55905 3
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  organization: Department of Molecular Genetics and Microbiology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico 87131, United States
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  givenname: Frank
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Issue 8
Keywords Mycobacterium tuberculosis
Mycobacteriales
Nitric oxide
Mycobacteriaceae
Bacteria
Actinomycetes
Activation
Antituberculous agent
Antibacterial agent
Isoniazid
Language English
License CC BY 4.0
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Deceased.
Corresponding author. Mailing address: College of Pharmacy, University of New Mexico Health Sciences Center, Albuquerque, NM 87131. Phone: (505) 272-4103. Fax: (505) 272-6749. E-mail: gtimmins@salud.unm.edu.
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Isonicotinic acid hydrazide (INH) is a frontline antituberculosis agent. Once taken up by Mycobacterium tuberculosis, INH requires activation by the...
Isonicotinic acid hydrazide (INH) is a frontline antituberculosis agent. Once taken up by Mycobacterium tuberculosis , INH requires activation by the...
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SubjectTerms Antibiotics. Antiinfectious agents. Antiparasitic agents
Antitubercular Agents
Antitubercular Agents - metabolism
Antitubercular Agents - pharmacology
Bacterial Proteins
Biological and medical sciences
Biotransformation
Catalase - metabolism
Free Radical Scavengers - pharmacology
Isoniazid
Isoniazid - metabolism
Isoniazid - pharmacology
Mechanisms of Action: Physiological Effects
Medical sciences
Mycobacterium bovis - metabolism
Mycobacterium tuberculosis
Mycobacterium tuberculosis - drug effects
Mycobacterium tuberculosis - genetics
Mycobacterium tuberculosis - metabolism
Nitric Oxide
Nitric Oxide - metabolism
Oxidoreductases
Oxidoreductases - genetics
Oxidoreductases - metabolism
Oxidoreductases - physiology
Peroxidase - metabolism
Peroxynitrous Acid - metabolism
Pharmacology. Drug treatments
Prodrugs - metabolism
Prodrugs - pharmacology
Spin Trapping
Tyrosine
Tyrosine - analogs & derivatives
Tyrosine - metabolism
Title Nitric Oxide Generated from Isoniazid Activation by KatG: Source of Nitric Oxide and Activity against Mycobacterium tuberculosis
URI http://aac.asm.org/content/48/8/3006.abstract
https://www.ncbi.nlm.nih.gov/pubmed/15273113
https://journals.asm.org/doi/10.1128/AAC.48.8.3006-3009.2004
https://search.proquest.com/docview/17720943
https://pubmed.ncbi.nlm.nih.gov/PMC478481
Volume 48
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