Nitric Oxide Generated from Isoniazid Activation by KatG: Source of Nitric Oxide and Activity against Mycobacterium tuberculosis
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 & Commerc...
Saved in:
Published in: | Antimicrobial Agents and Chemotherapy Vol. 48; no. 8; pp. 3006 - 3009 |
---|---|
Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Washington, DC
American Society for Microbiology
01-08-2004
|
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
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. 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 |
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 |
Author_xml | – sequence: 1 givenname: Graham S surname: TIMMINS fullname: TIMMINS, Graham S organization: College of Pharmacy, Toxicology Program, University of New Mexico Health Sciences Center, Albuquerque, New Mexico 87131, United States – sequence: 2 givenname: Sharon surname: MASTER fullname: MASTER, Sharon organization: Department of Molecular Genetics and Microbiology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico 87131, United States – sequence: 3 givenname: Frank surname: RUSNAK fullname: RUSNAK, Frank organization: Department of Biochemistry and Molecular Biology and Section of Hematology Research, Mayo Clinic and Foundation, Rochester, Minnesota 55905, United States – sequence: 4 givenname: Vojo surname: DERETIC fullname: DERETIC, Vojo organization: Department of Molecular Genetics and Microbiology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico 87131, United States |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15986171$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/15273113$$D View this record in MEDLINE/PubMed |
BookMark | eNqNkc1uEzEUhS1URNPCK4BZwG4G2-PxeJBYRBGEikIXwNpynOvE1YxdbE8hrHh0HCWi7Y7Ntaz7nft3ztCJDx4QekFJTSmTb-bzRc1lLeuGEFGV0NeMEP4IzSjpZSXaXpygWcmJikvCT9FZStek_NuePEGntGVdQ2kzQ3--uBydwVe_3BrwEjxEnWGNbQwjvkjBO_3brfHcZHerswser3b4k87Lt_hrmKIBHCx-UEP7I-7yDuuNdj5l_HlnwkqbDNFNI87TCqKZhpBceooeWz0keHZ8z9H3D--_LT5Wl1fLi8X8stIt57kCSSgTTcdAW2NETxorGGct5QyspIyuhGUAohXGWt311lrglrSG9WZtiG3O0btD3ZtpNcLagM9RD-omulHHnQraqYcZ77ZqE24V7ySXtOhfH_Ux_JggZTW6ZGAYtIcwJUW7jpGeNwXsDqCJIaUI9l8PStTePFXMU1wqqfbm7UOv9uYVJT8odRqZui7n9eUi_yF7fn-zu3ZHkwvw6gjoZPRgo_bGpXtcLwXt9iu-PHBbt9n-dBFUGURpbe7aNn8BSHrCTA |
CODEN | AACHAX |
CitedBy_id | crossref_primary_10_1016_j_pupt_2015_05_005 crossref_primary_10_1371_journal_pone_0181221 crossref_primary_10_1128_JB_188_7_2674_2680_2006 crossref_primary_10_1016_j_ijmyco_2015_06_006 crossref_primary_10_1016_j_bmcl_2013_03_006 crossref_primary_10_1016_j_ijmyco_2014_08_003 crossref_primary_10_1016_j_meegid_2016_09_004 crossref_primary_10_1128_AAC_00956_21 crossref_primary_10_1080_01443615_2022_2084370 crossref_primary_10_1134_S199075081202014X crossref_primary_10_1146_annurev_micro_61_111606_122346 crossref_primary_10_1016_j_bmcl_2019_06_015 crossref_primary_10_1186_s40360_020_0399_2 crossref_primary_10_1016_j_arabjc_2020_11_020 crossref_primary_10_1128_AAC_00453_10 crossref_primary_10_1016_j_molstruc_2018_05_082 crossref_primary_10_1111_j_1365_3156_2010_02665_x crossref_primary_10_1371_journal_pone_0069762 crossref_primary_10_1016_j_rechem_2022_100287 crossref_primary_10_1111_1751_7915_12035 crossref_primary_10_2174_1573406419666230111111153 crossref_primary_10_1007_s12017_016_8402_1 crossref_primary_10_1111_joim_12031 crossref_primary_10_1002_ardp_202000180 crossref_primary_10_1039_D2BM00752E crossref_primary_10_1007_s12272_017_0914_1 crossref_primary_10_4236_ojmm_2012_21004 crossref_primary_10_1007_s00044_019_02372_y crossref_primary_10_2174_1389557521666210219161045 crossref_primary_10_2217_fmb_14_125 crossref_primary_10_1021_mp300269g crossref_primary_10_1371_journal_pone_0039891 crossref_primary_10_2147_IDR_S456181 crossref_primary_10_1016_j_jct_2018_04_003 crossref_primary_10_1016_j_bmcl_2015_10_021 crossref_primary_10_3390_ijms222413259 crossref_primary_10_1016_j_bcp_2016_02_003 crossref_primary_10_1016_j_freeradbiomed_2019_07_012 crossref_primary_10_1021_ac701690d crossref_primary_10_1128_spectrum_03568_23 crossref_primary_10_3109_01443615_2014_958440 crossref_primary_10_1590_1678_4685_gmb_2022_0261 crossref_primary_10_1016_j_bmcl_2011_06_074 crossref_primary_10_1016_j_compbiolchem_2024_108034 crossref_primary_10_2174_1871526522666221004152324 crossref_primary_10_1007_s11664_016_4805_x crossref_primary_10_1111_j_1365_2958_2006_05467_x crossref_primary_10_1099_mic_0_001041 crossref_primary_10_1002_cmdc_201700424 crossref_primary_10_1002_slct_202002765 crossref_primary_10_18097_pbmc20135901081 crossref_primary_10_1002_cmdc_201500051 crossref_primary_10_1021_acs_jmedchem_0c01833 crossref_primary_10_1002_jcb_26032 crossref_primary_10_3390_antibiotics9050276 crossref_primary_10_1021_jm701048s crossref_primary_10_1074_jbc_M111_333385 crossref_primary_10_3109_08923973_2011_558095 crossref_primary_10_1111_bph_14867 crossref_primary_10_1134_S107042802001008X crossref_primary_10_1007_s11224_019_01425_7 crossref_primary_10_1002_slct_201600040 |
Cites_doi | 10.1111/j.1600-0773.1984.tb01916.x 10.1038/358591a0 10.1128/IAI.69.12.7711-7717.2001 10.1126/science.8284673 10.1016/S0021-9258(18)47160-8 10.1016/0003-9861(84)90147-4 10.1021/ja00095a063 10.1099/00221287-148-10-3139 10.1128/AAC.27.3.408 10.1016/0006-2952(94)90502-9 10.1016/S1286-4579(00)00359-2 10.1006/bbrc.1999.0358 10.1021/ja012271v 10.1124/mol.52.6.1081 10.1021/bi002614m 10.1086/514096 10.1038/nbt1196-1557 10.1021/ja9918674 10.1073/pnas.93.23.13212 10.1073/pnas.84.10.3189 10.1128/AAC.46.9.2765-2771.2002 10.1016/0925-4439(95)00061-8 10.1046/j.1365-2958.2002.03162.x 10.1084/jem.175.4.1111 10.1021/jo01119a010 10.1126/science.279.5347.98 10.1021/tx034188m 10.1054/tuld.1998.0203 10.1128/AAC.47.7.2299-2302.2003 10.1046/j.1365-2958.2000.02145.x 10.1126/science.280.5369.1607 |
ContentType | Journal Article |
Copyright | 2004 INIST-CNRS Copyright © 2004 American Society for Microbiology Copyright © 2004, American Society for Microbiology 2004 |
Copyright_xml | – notice: 2004 INIST-CNRS – notice: Copyright © 2004 American Society for Microbiology – notice: Copyright © 2004, American Society for Microbiology 2004 |
DBID | IQODW CGR CUY CVF ECM EIF NPM AAYXX CITATION 7QL C1K 5PM |
DOI | 10.1128/AAC.48.8.3006-3009.2004 |
DatabaseName | Pascal-Francis Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed CrossRef Bacteriology Abstracts (Microbiology B) Environmental Sciences and Pollution Management PubMed Central (Full Participant titles) |
DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) CrossRef Bacteriology Abstracts (Microbiology B) Environmental Sciences and Pollution Management |
DatabaseTitleList | CrossRef MEDLINE Bacteriology Abstracts (Microbiology B) |
Database_xml | – sequence: 1 dbid: ECM name: MEDLINE url: https://search.ebscohost.com/login.aspx?direct=true&db=cmedm&site=ehost-live sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Pharmacy, Therapeutics, & Pharmacology Biology |
EISSN | 1098-6596 |
EndPage | 3009 |
ExternalDocumentID | 10_1128_AAC_48_8_3006_3009_2004 0016-04 15273113 15986171 aac_48_8_3006 |
Genre | Research Support, U.S. Gov't, P.H.S Journal Article |
GrantInformation_xml | – fundername: NCRR NIH HHS grantid: P20 RR015636 – fundername: NIAID NIH HHS grantid: AI42999 – fundername: NCRR NIH HHS grantid: P20 RR15636 – fundername: NIAID NIH HHS grantid: R01 AI042999 – fundername: NIAID NIH HHS grantid: R37 AI042999 |
GroupedDBID | --- .55 .GJ 08R 0R~ 23M 2WC 39C 3O- 4.4 53G 5GY 5RE 5VS 6J9 AAPBV AAUGY ACGFO ADBBV AENEX AFMIJ AGNAY AI. ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL BTFSW C1A CS3 DIK E3Z EBS EJD F5P FRP GX1 H13 HH5 HYE HZ~ H~9 IQODW J5H K-O KQ8 L7B LSO MVM NEJ O9- OK1 P2P RHF RHI RNS RPM RSF TR2 UHB VH1 W2D W8F WH7 WHG WOQ X7M X7N XOL Y6R ZA5 ZGI ZXP ~A~ AGVNZ CGR CUY CVF ECM EIF NPM - 0R 55 A ABFLS ADACO ADBIT BXI GJ HZ AAYXX CITATION 7QL C1K 5PM |
ID | FETCH-LOGICAL-a544t-e80126372eafcc6903f62425142ef8121b6f2ee656cffa79fffe4f05c29cdc0f3 |
IEDL.DBID | RPM |
ISSN | 0066-4804 |
IngestDate | Tue Sep 17 21:19:17 EDT 2024 Fri Oct 25 02:04:09 EDT 2024 Thu Nov 21 21:13:56 EST 2024 Tue Dec 28 13:59:06 EST 2021 Sat Nov 02 12:21:42 EDT 2024 Sun Oct 22 16:04:11 EDT 2023 Wed May 18 15:33:49 EDT 2016 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 8 |
Keywords | Mycobacterium tuberculosis Mycobacteriales Nitric oxide Mycobacteriaceae Bacteria Actinomycetes Activation Antituberculous agent Antibacterial agent Isoniazid |
Language | English |
License | CC BY 4.0 |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-a544t-e80126372eafcc6903f62425142ef8121b6f2ee656cffa79fffe4f05c29cdc0f3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 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. |
OpenAccessLink | https://europepmc.org/articles/pmc478481?pdf=render |
PMID | 15273113 |
PQID | 17720943 |
PQPubID | 23462 |
PageCount | 4 |
ParticipantIDs | asm2_journals_10_1128_AAC_48_8_3006_3009_2004 proquest_miscellaneous_17720943 crossref_primary_10_1128_AAC_48_8_3006_3009_2004 pubmed_primary_15273113 pascalfrancis_primary_15986171 pubmedcentral_primary_oai_pubmedcentral_nih_gov_478481 highwire_asm_aac_48_8_3006 |
PublicationCentury | 2000 |
PublicationDate | 2004-08-01 |
PublicationDateYYYYMMDD | 2004-08-01 |
PublicationDate_xml | – month: 08 year: 2004 text: 2004-08-01 day: 01 |
PublicationDecade | 2000 |
PublicationPlace | Washington, DC |
PublicationPlace_xml | – name: Washington, DC – name: United States |
PublicationTitle | Antimicrobial Agents and Chemotherapy |
PublicationTitleAbbrev | AAC |
PublicationTitleAlternate | Antimicrob Agents Chemother |
PublicationYear | 2004 |
Publisher | American Society for Microbiology |
Publisher_xml | – name: American Society for Microbiology |
References | e_1_3_2_27_2 e_1_3_2_28_2 e_1_3_2_21_2 e_1_3_2_22_2 e_1_3_2_23_2 e_1_3_2_25_2 (e_1_3_2_19_2) 1984; 229 e_1_3_2_9_2 (e_1_3_2_10_2) 1997; 2 e_1_3_2_15_2 e_1_3_2_38_2 e_1_3_2_8_2 e_1_3_2_16_2 e_1_3_2_37_2 (e_1_3_2_3_2) 1994; 375 e_1_3_2_7_2 e_1_3_2_17_2 e_1_3_2_6_2 (e_1_3_2_26_2) 2004; 17 (e_1_3_2_24_2) 1984; 54 e_1_3_2_30_2 e_1_3_2_32_2 e_1_3_2_31_2 e_1_3_2_5_2 e_1_3_2_11_2 e_1_3_2_34_2 e_1_3_2_4_2 e_1_3_2_12_2 e_1_3_2_33_2 e_1_3_2_13_2 e_1_3_2_36_2 e_1_3_2_2_2 e_1_3_2_14_2 (e_1_3_2_35_2) 1969; 99 (e_1_3_2_29_2) 1999; 121 (e_1_3_2_20_2) 1997; 283 (e_1_3_2_18_2) 1998; 217 |
References_xml | – volume: 54 start-page: 189 year: 1984 ident: e_1_3_2_24_2 publication-title: Acta Pharmacol. Toxicol. doi: 10.1111/j.1600-0773.1984.tb01916.x – ident: e_1_3_2_38_2 doi: 10.1038/358591a0 – volume: 2 start-page: 2167 year: 1997 ident: e_1_3_2_10_2 publication-title: J. Chem. Soc. Perkin Trans. I – ident: e_1_3_2_23_2 doi: 10.1128/IAI.69.12.7711-7717.2001 – ident: e_1_3_2_2_2 doi: 10.1126/science.8284673 – ident: e_1_3_2_22_2 doi: 10.1016/S0021-9258(18)47160-8 – volume: 229 start-page: 220 year: 1984 ident: e_1_3_2_19_2 publication-title: Arch. Biochem. Biophys. doi: 10.1016/0003-9861(84)90147-4 – volume: 99 start-page: 729 year: 1969 ident: e_1_3_2_35_2 publication-title: Am. Rev. Respir. Dis. – ident: e_1_3_2_13_2 doi: 10.1021/ja00095a063 – ident: e_1_3_2_16_2 doi: 10.1099/00221287-148-10-3139 – ident: e_1_3_2_25_2 doi: 10.1128/AAC.27.3.408 – ident: e_1_3_2_34_2 – volume: 217 start-page: 209 year: 1998 ident: e_1_3_2_18_2 publication-title: Novartis Found. Symp. – ident: e_1_3_2_30_2 doi: 10.1016/0006-2952(94)90502-9 – ident: e_1_3_2_27_2 doi: 10.1016/S1286-4579(00)00359-2 – ident: e_1_3_2_31_2 doi: 10.1006/bbrc.1999.0358 – ident: e_1_3_2_11_2 doi: 10.1021/ja012271v – ident: e_1_3_2_12_2 doi: 10.1124/mol.52.6.1081 – ident: e_1_3_2_32_2 doi: 10.1021/bi002614m – ident: e_1_3_2_33_2 doi: 10.1086/514096 – ident: e_1_3_2_8_2 doi: 10.1038/nbt1196-1557 – volume: 121 start-page: 10962 year: 1999 ident: e_1_3_2_29_2 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja9918674 – ident: e_1_3_2_37_2 doi: 10.1073/pnas.93.23.13212 – ident: e_1_3_2_5_2 doi: 10.1073/pnas.84.10.3189 – ident: e_1_3_2_4_2 doi: 10.1128/AAC.46.9.2765-2771.2002 – ident: e_1_3_2_14_2 doi: 10.1016/0925-4439(95)00061-8 – ident: e_1_3_2_15_2 doi: 10.1046/j.1365-2958.2002.03162.x – ident: e_1_3_2_6_2 doi: 10.1084/jem.175.4.1111 – ident: e_1_3_2_9_2 doi: 10.1021/jo01119a010 – ident: e_1_3_2_21_2 doi: 10.1126/science.279.5347.98 – volume: 17 start-page: 234 year: 2004 ident: e_1_3_2_26_2 publication-title: Chem. Res. Toxicol. doi: 10.1021/tx034188m – ident: e_1_3_2_36_2 doi: 10.1054/tuld.1998.0203 – volume: 375 start-page: 81 year: 1994 ident: e_1_3_2_3_2 publication-title: Biol. Chem. Hoppe-Seyler – ident: e_1_3_2_7_2 doi: 10.1128/AAC.47.7.2299-2302.2003 – ident: e_1_3_2_28_2 doi: 10.1046/j.1365-2958.2000.02145.x – ident: e_1_3_2_17_2 doi: 10.1126/science.280.5369.1607 – volume: 283 start-page: 138 year: 1997 ident: e_1_3_2_20_2 publication-title: J. Pharmacol. Exp. Ther. |
SSID | ssj0006590 |
Score | 2.1202338 |
Snippet | Classifications
Services
AAC
Citing Articles
Google Scholar
PubMed
Related Content
Social Bookmarking
CiteULike
Delicious
Digg
Facebook
Google+
Mendeley
Reddit... 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... |
SourceID | pubmedcentral proquest crossref asm2 pubmed pascalfrancis highwire |
SourceType | Open Access Repository Aggregation Database Index Database Publisher |
StartPage | 3006 |
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 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3Nb9MwFH-ik0Bc0ChfGVB8QDstaT6cj3KrysamqaPShsTNchwbIq3ptDQS2Yk_nWc7oQtCQuLSS203rd_z-736934P4L3MBJc51W1Sqe_SJCrcjMfclVEQ6PwZ7UYniqeX6cXX7OOxlsmhfS2MIe2LvPSq67VXld8Nt_JmLaY9T2y6Wi5oqkXgpyMYITTsM_Tu9E1i-78KhlKXZj7tOF14DE_n84VHMy_zIt8QvnxTqNJ15knx4SI8l3m9DocxqtcN1rRJXuMvp2zLi79h0j-plfdi1ck-POlAJpnbL_MUHshqDA9t28l2DI-W3YX6GA5XVrq6PSJXu0qs-ogcktVO1Lp9Bj8vSq3lTz7_KAtJrFg1glWiy1PIGYL2kt-VBZmLvl0ayVtyzrefPpBLcz9ANooM1uBVNxzzAMK_8RKBKlm2Ag8YIyDdrMm2yeWtaK43dVk_hy8nx1eLU7fr3uDymNKtK3XsS6I0lFwJgUl4pHQtCgK0UCqEFUGeqFBKxJNCKZ7OlFKSKj8W4UwUwlfRC9irNpV8BSSZxYhKCo7ojyPAxPCCa1KRxBh_8cSNHHD1trHO_WpmMpswY7jjjGYsY3rH9ctMt92kDvj9_rIbK-rx7ykHvR0w_CzGudgNc2AysIzdolr9PkgDB971psLQffWdDK_kpsEnxexGkzsdeGkN595ca5MOJAOT-j1AC4MP30F_MQLh1j8O_nfia3hs-Uma5vgG9ra3jXwLo7poJph0nJ1PjMf9AusnKdw |
link.rule.ids | 230,315,729,782,786,887,27933,27934,53800,53802 |
linkProvider | National Library of Medicine |
linkToHtml | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9NAEB7RIh4XHqGAC7R7QD3Vjh_rR7hFoSVVmxCpQeK2Wq93wVLjVHUsYU78dGa9NqkRElIvvnh37STfznyTnfkG4L1MBJcp1W1SqWvTKMjshIfcloHn6fgZcaMDxellPP-afDzRMjm0q4VpkvZFmjvF1cop8u9NbuX1Sgy7PLHhYjahsRaBH-7AfdyurtvF6K39jULzzwo6U5smLm2zutAQD8fjiUMTJ3ECt0n5cptSlbY3T4yvF6Bl5uXK73upTjlYJ07yEr87ZZpe_IuV_p1cectbnT692-d8Bk9adkrG5u5zuCeLATww_SrrATyctSfxAzhaGM3r-pgstyVc5TE5IoutGnb9An7Nc90EgHz-kWeSGJVrZLlE17WQM2T7Of-ZZ2Qsuj5rJK3JOd98-kAum4MFslaktwYv2uEYQBD-jefIcMmsFmiZGuXpakU2VSpvRHW1LvNyD76cniwnU7tt-2DzkNKNLbXTjILYl1wJgdF7oHQRCzI7XyrkI14aKV9KJKJCKR6PlFKSKjcU_khkwlXBS9gt1oV8DSQahUhnMo60kSMzRb-Ea1IRhei40VQHFtj612btvi1ZExL5CUOgMJqwhGmg6MtI9-ukFrgdLNi1UQP5_5T9Dj4Mn8U4F9thFhz0ALVdVMvme7FnwWGHMIb7Xh_m8EKuK3xTDIt0VqgFrwzebs01ULYg6iHxzwCtKN6_gwBslMUN4PbvOvEQHk2Xswt2cTY_fwOPTZKTzpV8C7ubm0q-g50yqw6a7fob3MI-Og |
linkToPdf | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9NAEB7RIiouPAIFF2j3gHqq49f6EW5R2tCqJERqkbit1utdsNQ4UR1LmBM_nVmvTWqEhNRLLt7dOPG3M994Z74BeC8TwWVKdZtU6to0CjI74SG3ZeB5On5G3OhA8fwqnn9NTs-0TE7S1cI0SfsizYfFzXJY5N-b3Mr1UjhdnpizmE1orEXgnXWmnB14iFvW9bs4vbXBUWjerqBDtWni0jazC42xMx5PhjQZJsPAbdK-3KZcpe3PE-MtBmidebn0-56qUw_WyZO8xP9PmcYX_2KmfydY3vFY06f3_63P4EnLUsnYjHgOD2QxgEemb2U9gL1ZeyI_gOOF0b6uT8j1tpSrPCHHZLFVxa5fwK95rpsBkM8_8kwSo3aNbJfo-hZygaw_5z_zjIxF12-NpDW55JuPH8hVc8BAVor01uBFOxwDCcK_8RyZLpnVAi1Uo0BdLcmmSuWtqG5WZV6-hC_Ts-vJud22f7B5SOnGltp5RkHsS66EwCg-ULqYBRmeLxXyEi-NlC8lElKhFI9HSilJlRsKfyQy4apgH3aLVSFfA4lGIdKajCN95MhQ0T_hmlREITpwNNmBBbZ-4qzdvyVrQiM_YQgWRhOWMA0W_THSfTupBW4HDbY2qiD_n3LQQYjhdzHOxXaYBYc9UG0X1fL5XuxZcNShjOH-14c6vJCrCu8UwyOdHWrBK4O5O3MNnC2Iemj8M0Ari_evIAgbhXEDuoP7TjyCvcXplH26mF--gccm10mnTL6F3c1tJd_BTplVh82O_Q3lMUC6 |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Nitric+Oxide+Generated+from+Isoniazid+Activation+by+KatG%3A+Source+of+Nitric+Oxide+and+Activity+against+Mycobacterium+tuberculosis&rft.jtitle=Antimicrobial+agents+and+chemotherapy&rft.au=Timmins%2C+Graham+S&rft.au=Master%2C+Sharon&rft.au=Rusnak%2C+Frank&rft.au=Deretic%2C+Vojo&rft.date=2004-08-01&rft.issn=0066-4804&rft.volume=48&rft.issue=8&rft.spage=3006&rft.epage=3009&rft_id=info:doi/10.1128%2FAAC.48.8.3006-3009.2004&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0066-4804&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0066-4804&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0066-4804&client=summon |