Literature DB >> 27075937

Nitrite and nitroso compounds can serve as specific catalase inhibitors.

Vladimir Yu Titov1, Anatoly N Osipov1.   

Abstract

OBJECTIVE: We present evidence that nitrite and nitrosothiols, nitrosoamines and non-heme dinitrosyl iron complexes can reversibly inhibit catalase with equal effectiveness.
METHODS: Catalase activity was evaluated by the permanganatometric and calorimetric assays.
RESULTS: This inhibition is not the result of chemical transformations of these compounds to a single inhibitor, as well as it is not the result of NO release from these substances (as NO traps have no effect on the extent of inhibition). It was found that chloride and bromide in concentration above 80 mM and thiocyanate in concentration above 20 μM enhance catalase inhibition by nitrite and the nitroso compounds more than 100 times. The inhibition degree in this case is comparable with that induced by azide. DISCUSSION: We propose that the direct catalase inhibitor is a positively charged NO-group. This group acquires a positive charge in the active center of enzyme by interaction of nitrite or nitroso compounds with some enzyme groups. Halides and thiocyanate protect the NO+ group from hydration and thus increase its inhibition effect. It is probable that a comparatively low chloride concentration in many cells is the main factor to protect catalase from inhibition by nitrite and nitroso compounds.

Entities:  

Keywords:  Catalase; Dinitrosyl iron complex; Haem-containing peroxidase; Halide ions; Inhibition; Nitrite; S-nitrosothiols; Thiocyanate

Mesh:

Substances:

Year:  2016        PMID: 27075937      PMCID: PMC6837560          DOI: 10.1080/13510002.2016.1168589

Source DB:  PubMed          Journal:  Redox Rep        ISSN: 1351-0002            Impact factor:   4.412


  19 in total

Review 1.  Methods for detection of reactive metabolites of oxygen and nitrogen: in vitro and in vivo considerations.

Authors:  Margaret M Tarpey; David A Wink; Matthew B Grisham
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2004-03       Impact factor: 3.619

2.  GENERATION OF HYDROGEN PEROXIDE DURING THE REACTION OF NITRATE WITH OXYHEMOGLOBIN.

Authors:  G COHEN; M MARTINEZ; P HOCHSTEIN
Journal:  Biochemistry       Date:  1964-07       Impact factor: 3.162

Review 3.  Formation of N-nitroso compounds: chemistry, kinetics, and in vivo occurrence.

Authors:  S S Mirvish
Journal:  Toxicol Appl Pharmacol       Date:  1975-03       Impact factor: 4.219

4.  Use of ascorbic acid to inhibit nitrosation: kinetic and mass transfer considerations for an in vitro system.

Authors:  W R Licht; S R Tannenbaum; W M Deen
Journal:  Carcinogenesis       Date:  1988-03       Impact factor: 4.944

5.  Reversible binding and inhibition of catalase by nitric oxide.

Authors:  G C Brown
Journal:  Eur J Biochem       Date:  1995-08-15

6.  Nitrite-catalase interaction as an important element of nitrite toxicity.

Authors:  V Yu Titov; Yu M Petrenko
Journal:  Biochemistry (Mosc)       Date:  2003-06       Impact factor: 2.487

7.  Inhibition of catalase activity in vitro by diesel exhaust particles.

Authors:  Y Mori; S Murakami; T Sagae; H Hayashi; M Sakata; M Sagai; Y Kumagai
Journal:  J Toxicol Environ Health       Date:  1996-02-09

Review 8.  Dinitrosyl iron complexes with thiolate ligands: physico-chemistry, biochemistry and physiology.

Authors:  Anatoly F Vanin
Journal:  Nitric Oxide       Date:  2009-04-12       Impact factor: 4.427

9.  Interaction of nitric oxide with catalase: structural and kinetic analysis.

Authors:  Namrta Purwar; Jennifer M McGarry; Joshua Kostera; A Andrew Pacheco; Marius Schmidt
Journal:  Biochemistry       Date:  2011-05-06       Impact factor: 3.162

10.  Sodium, potassium, and chloride fluxes in intercostal muscle from normal goats and goats with hereditary myotonia.

Authors:  R J Lipicky; S H Bryant
Journal:  J Gen Physiol       Date:  1966-09       Impact factor: 4.086

View more
  3 in total

1.  Proton motive force underpins respiration-mediated potentiation of aminoglycoside lethality in pathogenic Escherichia coli.

Authors:  Calum M Webster; Ayrianna M Woody; Safura Fusseini; Louis G Holmes; Gary K Robinson; Mark Shepherd
Journal:  Arch Microbiol       Date:  2022-01-06       Impact factor: 2.552

2.  Endogenous Hemoprotein-Dependent Signaling Pathways of Nitric Oxide and Nitrite.

Authors:  Matthew R Dent; Anthony W DeMartino; Jesús Tejero; Mark T Gladwin
Journal:  Inorg Chem       Date:  2021-07-27       Impact factor: 5.436

3.  Long-lasting blood pressure lowering effects of nitrite are NO-independent and mediated by hydrogen peroxide, persulfides, and oxidation of protein kinase G1α redox signalling.

Authors:  Martin Feelisch; Takaaki Akaike; Kayleigh Griffiths; Tomoaki Ida; Oleksandra Prysyazhna; Joanna J Goodwin; Nicholas D Gollop; Bernadette O Fernandez; Magdalena Minnion; Miriam M Cortese-Krott; Alessandra Borgognone; Rosie M Hayes; Philip Eaton; Michael P Frenneaux; Melanie Madhani
Journal:  Cardiovasc Res       Date:  2020-01-01       Impact factor: 10.787

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.