Reactions of N-N and N-O compounds with horseradish peroxidase and peroxidases from Mycobacterium tuberculosis
(1999) In APMIS : acta pathologica, microbiologica, et immunologica Scandinavica 107(6). p.555-565- Abstract
- Several N-N-and N-O-containing compounds were analysed for their ability to act as substrates for horseradish peroxidase and peroxidases in Mycobacterium tuberculosis extracts. Aminoguanidine, diaminoguanidine, isoniazid, hydroxylamine and hydrazine were found to be weak substrates for horseradish peroxidase in reaction I and to inhibit the reaction of horseradish peroxidase with hydrogen peroxide. The same compounds inhibited the reaction of Mycobacterium tuberculosis peroxidase-catalase with hydrogen peroxide, and hydroxylamine was found to be a weak substrate for this enzyme. In growth inhibition experiments, diaminoguanidine inhibited the growth of M. tuberculosis H37Rv at 50 microg/mL, but not the growth of two isoniazid-resistant... (More)
- Several N-N-and N-O-containing compounds were analysed for their ability to act as substrates for horseradish peroxidase and peroxidases in Mycobacterium tuberculosis extracts. Aminoguanidine, diaminoguanidine, isoniazid, hydroxylamine and hydrazine were found to be weak substrates for horseradish peroxidase in reaction I and to inhibit the reaction of horseradish peroxidase with hydrogen peroxide. The same compounds inhibited the reaction of Mycobacterium tuberculosis peroxidase-catalase with hydrogen peroxide, and hydroxylamine was found to be a weak substrate for this enzyme. In growth inhibition experiments, diaminoguanidine inhibited the growth of M. tuberculosis H37Rv at 50 microg/mL, but not the growth of two isoniazid-resistant strains. Isonicotinic acid hydroxamate inhibited the reaction of the peroxidases with hydrogen peroxide, but was not itself a substrate and had no growth-inhibitory effects. On the basis of these results we suggest that the effect of isoniazid on growth of M. tuberculosis results from increased oxidative stress due to inhibition of catalase-peroxidase as well as from generation of toxic radicals with the structure [structure in text]. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1114990
- author
- Brimnes, J ; Miörner, Håkan LU ; Anthoni, U ; Bruun, L and Houen, G
- organization
- publishing date
- 1999
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Peroxidase, isoniazid, aminoguanidine, diaminoguanidine, Mycobacterium tuberculosis, drug resistance
- in
- APMIS : acta pathologica, microbiologica, et immunologica Scandinavica
- volume
- 107
- issue
- 6
- pages
- 555 - 565
- publisher
- John Wiley & Sons Inc.
- external identifiers
-
- pmid:10379683
- scopus:0033032220
- ISSN
- 1600-0463
- language
- English
- LU publication?
- yes
- id
- fc115477-b4dd-4abf-ba00-2778f57b0929 (old id 1114990)
- date added to LUP
- 2016-04-01 11:49:32
- date last changed
- 2022-03-20 19:33:35
@article{fc115477-b4dd-4abf-ba00-2778f57b0929,
abstract = {{Several N-N-and N-O-containing compounds were analysed for their ability to act as substrates for horseradish peroxidase and peroxidases in Mycobacterium tuberculosis extracts. Aminoguanidine, diaminoguanidine, isoniazid, hydroxylamine and hydrazine were found to be weak substrates for horseradish peroxidase in reaction I and to inhibit the reaction of horseradish peroxidase with hydrogen peroxide. The same compounds inhibited the reaction of Mycobacterium tuberculosis peroxidase-catalase with hydrogen peroxide, and hydroxylamine was found to be a weak substrate for this enzyme. In growth inhibition experiments, diaminoguanidine inhibited the growth of M. tuberculosis H37Rv at 50 microg/mL, but not the growth of two isoniazid-resistant strains. Isonicotinic acid hydroxamate inhibited the reaction of the peroxidases with hydrogen peroxide, but was not itself a substrate and had no growth-inhibitory effects. On the basis of these results we suggest that the effect of isoniazid on growth of M. tuberculosis results from increased oxidative stress due to inhibition of catalase-peroxidase as well as from generation of toxic radicals with the structure [structure in text].}},
author = {{Brimnes, J and Miörner, Håkan and Anthoni, U and Bruun, L and Houen, G}},
issn = {{1600-0463}},
keywords = {{Peroxidase; isoniazid; aminoguanidine; diaminoguanidine; Mycobacterium tuberculosis; drug resistance}},
language = {{eng}},
number = {{6}},
pages = {{555--565}},
publisher = {{John Wiley & Sons Inc.}},
series = {{APMIS : acta pathologica, microbiologica, et immunologica Scandinavica}},
title = {{Reactions of N-N and N-O compounds with horseradish peroxidase and peroxidases from Mycobacterium tuberculosis}},
volume = {{107}},
year = {{1999}},
}