Literature DB >> 10813647

Chemiluminescent aldehyde and beta-diketone reactions promoted by peroxynitrite.

F S Knudsen1, C A Penatti, L O Royer, K A Bidart, M Christoff, D Ouchi, E J Bechara.   

Abstract

Peroxynitrite is shown here to promote the aerobic oxidation of isobutanal (IBAL) and 3-methyl-2,4-pentanedione (MP) in a pH 7.2 phosphate buffer into acetone plus formate and biacetyl plus acetate, respectively. These products are expected from dioxetane intermediates, whose thermolysis is known to be chemiluminescent (CL). Accordingly, the extent of total oxygen uptake by IBAL at different concentrations parallels the corresponding CL maximum intensities. The pH profile based on oxygen uptake data for the MP reaction matches the titration curve of peroxynitrous acid (pK(a) approximately 7), indicating that peroxynitrite anion is the oxidizing agent. Energy transfer studies with IBAL and the 9, 10-dibromoanthracene-2-sulfonate ion, a triplet carbonyl detector, indicates that triplet acetone (tau = 19 micros) is the energy donor. It is postulated that IBAL- or MP-generated triplet carbonyls are produced by the thermolysis of dioxetane intermediates, which are formed by the cyclization of alpha-hydroperoxide intermediates produced by insertion of dioxygen into the IBAL or MP enolyl radicals, followed by their reduction. Accordingly, EPR spin-trapping studies with 3,5-dibromo-4-nitrosobenzenesulfonic acid (DBNBS) and 2-methyl-2-nitrosopropane (MNP) revealed the intermediacy of carbon-centered radicals, as expected for one-electron abstraction from the enol forms of IBAL or MP by peroxynitrite. The EPR data obtained with IBAL also reveal formation of the isopropyl radical produced by competitive nucleophilic addition of ONOO(-) to IBAL, followed by homolytic cleavage of this adduct and beta-scission of the resulting Me(2)CHCH(O(-))O(*). Superstoichiometric formation of fragmentation products from IBAL or MP attests to the prevalence of an autoxidation chain reaction, here proposed to be initiated by one-electron abstraction by ONOO(-) from the substrate. This work reveals the potential role of peroxynitrite as a generator of electronically excited species that may contribute to deleterious and pathological processes associated with excessive nitric oxide and aldehyde production.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10813647     DOI: 10.1021/tx990176i

Source DB:  PubMed          Journal:  Chem Res Toxicol        ISSN: 0893-228X            Impact factor:   3.739


  5 in total

1.  Myoglobin-H2O2 catalyzes the oxidation of β-ketoacids to α-dicarbonyls: mechanism and implications in ketosis.

Authors:  Douglas Ganini; Marcelo Christoff; Marilyn Ehrenshaft; Maria B Kadiiska; Ronald P Mason; Etelvino J H Bechara
Journal:  Free Radic Biol Med       Date:  2011-05-08       Impact factor: 7.376

2.  Photochemistry. Chemiexcitation of melanin derivatives induces DNA photoproducts long after UV exposure.

Authors:  Sanjay Premi; Silvia Wallisch; Camila M Mano; Adam B Weiner; Antonella Bacchiocchi; Kazumasa Wakamatsu; Etelvino J H Bechara; Ruth Halaban; Thierry Douki; Douglas E Brash
Journal:  Science       Date:  2015-02-20       Impact factor: 47.728

Review 3.  Chemical excitation of electrons: A dark path to melanoma.

Authors:  Sanjay Premi; Douglas E Brash
Journal:  DNA Repair (Amst)       Date:  2016-06-01

4.  Formation of 2-nitrophenol from salicylaldehyde as a suitable test for low peroxynitrite fluxes.

Authors:  Yuliya Mikhed; Kai Bruns; Stefan Schildknecht; Michael Jörg; Mobin Dib; Matthias Oelze; Karl J Lackner; Thomas Münzel; Volker Ullrich; Andreas Daiber
Journal:  Redox Biol       Date:  2015-11-27       Impact factor: 11.799

5.  Acetyl zingerone: An efficacious multifunctional ingredient for continued protection against ongoing DNA damage in melanocytes after sun exposure ends.

Authors:  R K Chaudhuri; T Meyer; S Premi; D Brash
Journal:  Int J Cosmet Sci       Date:  2019-12-17       Impact factor: 2.970

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.