Myoglobin-H2O2 catalyzes the oxidation of beta-ketoacids to alpha-dicarbonyls: Mechanism and implications in ketosis

Detalhes bibliográficos
Autor(a) principal: Ganini, Douglas
Data de Publicação: 2011
Outros Autores: Christoff, Marcelo, Ehrenshaft, Marilyn, Kadiiska, Maria B., Mason, Ronald P., Bechara, Etelvino José Henriques [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1016/j.freeradbiomed.2011.05.002
http://repositorio.unifesp.br/handle/11600/33896
Resumo: Acetoacetate (AA) and 2-methylacetoacetate (MAA) are accumulated in metabolic disorders such as diabetes and isoleucinemia. Here we examine the mechanism of AA and MAA aerobic oxidation initiated by myoglobin (Mb)/H2O2. We propose a chemiluminescent route involving a dioxetanone intermediate whose thermolysis yields triplet alpha-dicarbonyl species (methylglyoxal and diacetyl). the observed ultraweak chemiluminescence increased linearly on raising the concentration of either Mb (10-500 mu M) or AA (10-100 mM). Oxygen uptake studies revealed that MAA is almost a 100-fold more reactive than AA. EPR spin-trapping studies with MNP/MAA revealed the intermediacy of an alpha-carbon-centered radical and acetyl radical. the latter radical, probably derived from triplet diacetyl, is totally suppressed by sorbate, a well-known quencher of triplet carbonyls. Furthermore, an EPR signal assignable to MNP-AA(center dot) adduct was observed and confirmed by isotope effects. Oxygen consumption and a-dicarbonyl yield were shown to be dependent on AA or MAA concentrations (1-50 mM) and on H2O2 or tert-butOOH added to the Mb-containing reaction mixtures. That ferrylMb is involved in a peroxidase cycle acting on the substrates is suggested by the reaction pH profiles and immunospin-trapping experiments. the generation of radicals and triplet dicarbonyl products by Mb/H2O2/beta-ketoacids may contribute to the adverse health effects of ketogenic unbalance. (C) 2011 Elsevier Inc. All rights reserved.
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spelling Myoglobin-H2O2 catalyzes the oxidation of beta-ketoacids to alpha-dicarbonyls: Mechanism and implications in ketosisMyoglobinAcetoacetate2-MethylacetoacetateFree radicalsTriplet carbonylsMethylglyoxalDiacetylKetosisAcetoacetate (AA) and 2-methylacetoacetate (MAA) are accumulated in metabolic disorders such as diabetes and isoleucinemia. Here we examine the mechanism of AA and MAA aerobic oxidation initiated by myoglobin (Mb)/H2O2. We propose a chemiluminescent route involving a dioxetanone intermediate whose thermolysis yields triplet alpha-dicarbonyl species (methylglyoxal and diacetyl). the observed ultraweak chemiluminescence increased linearly on raising the concentration of either Mb (10-500 mu M) or AA (10-100 mM). Oxygen uptake studies revealed that MAA is almost a 100-fold more reactive than AA. EPR spin-trapping studies with MNP/MAA revealed the intermediacy of an alpha-carbon-centered radical and acetyl radical. the latter radical, probably derived from triplet diacetyl, is totally suppressed by sorbate, a well-known quencher of triplet carbonyls. Furthermore, an EPR signal assignable to MNP-AA(center dot) adduct was observed and confirmed by isotope effects. Oxygen consumption and a-dicarbonyl yield were shown to be dependent on AA or MAA concentrations (1-50 mM) and on H2O2 or tert-butOOH added to the Mb-containing reaction mixtures. That ferrylMb is involved in a peroxidase cycle acting on the substrates is suggested by the reaction pH profiles and immunospin-trapping experiments. the generation of radicals and triplet dicarbonyl products by Mb/H2O2/beta-ketoacids may contribute to the adverse health effects of ketogenic unbalance. (C) 2011 Elsevier Inc. All rights reserved.Universidade Federal de São Paulo, Dept Ciencias Exatas & Terra, Inst Ciencias Ambientais Quim & Farmaceut, BR-00972270 Diadema, SP, BrazilUniv São Paulo, Inst Quim, Dept Bioquim, BR-01498 São Paulo, BrazilNatl Inst Environm Hlth Sci, Free Rad Metab Grp, Lab Toxicol & Pharmacol, NIH, Res Triangle Pk, NC 27709 USAUniversidade Federal de São Paulo, Dept Ciencias Exatas & Terra, Inst Ciencias Ambientais Quim & Farmaceut, BR-00972270 Diadema, SP, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Instituto Nacional de Ciencia e Tecnologia (INCT) RedoxomaNational Institute of Environmental Health Sciences (NIEHS)Elsevier B.V.Universidade Federal de São Paulo (UNIFESP)Universidade de São Paulo (USP)Natl Inst Environm Hlth SciGanini, DouglasChristoff, MarceloEhrenshaft, MarilynKadiiska, Maria B.Mason, Ronald P.Bechara, Etelvino José Henriques [UNIFESP]2016-01-24T14:17:01Z2016-01-24T14:17:01Z2011-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion733-743application/pdfhttp://dx.doi.org/10.1016/j.freeradbiomed.2011.05.002Free Radical Biology and Medicine. New York: Elsevier B.V., v. 51, n. 3, p. 733-743, 2011.10.1016/j.freeradbiomed.2011.05.002WOS000292856900017.pdf0891-5849http://repositorio.unifesp.br/handle/11600/33896WOS:000292856900017engFree Radical Biology and Medicineinfo:eu-repo/semantics/openAccesshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policyreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-31T18:41:23Zoai:repositorio.unifesp.br/:11600/33896Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-31T18:41:23Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Myoglobin-H2O2 catalyzes the oxidation of beta-ketoacids to alpha-dicarbonyls: Mechanism and implications in ketosis
title Myoglobin-H2O2 catalyzes the oxidation of beta-ketoacids to alpha-dicarbonyls: Mechanism and implications in ketosis
spellingShingle Myoglobin-H2O2 catalyzes the oxidation of beta-ketoacids to alpha-dicarbonyls: Mechanism and implications in ketosis
Ganini, Douglas
Myoglobin
Acetoacetate
2-Methylacetoacetate
Free radicals
Triplet carbonyls
Methylglyoxal
Diacetyl
Ketosis
title_short Myoglobin-H2O2 catalyzes the oxidation of beta-ketoacids to alpha-dicarbonyls: Mechanism and implications in ketosis
title_full Myoglobin-H2O2 catalyzes the oxidation of beta-ketoacids to alpha-dicarbonyls: Mechanism and implications in ketosis
title_fullStr Myoglobin-H2O2 catalyzes the oxidation of beta-ketoacids to alpha-dicarbonyls: Mechanism and implications in ketosis
title_full_unstemmed Myoglobin-H2O2 catalyzes the oxidation of beta-ketoacids to alpha-dicarbonyls: Mechanism and implications in ketosis
title_sort Myoglobin-H2O2 catalyzes the oxidation of beta-ketoacids to alpha-dicarbonyls: Mechanism and implications in ketosis
author Ganini, Douglas
author_facet Ganini, Douglas
Christoff, Marcelo
Ehrenshaft, Marilyn
Kadiiska, Maria B.
Mason, Ronald P.
Bechara, Etelvino José Henriques [UNIFESP]
author_role author
author2 Christoff, Marcelo
Ehrenshaft, Marilyn
Kadiiska, Maria B.
Mason, Ronald P.
Bechara, Etelvino José Henriques [UNIFESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Universidade de São Paulo (USP)
Natl Inst Environm Hlth Sci
dc.contributor.author.fl_str_mv Ganini, Douglas
Christoff, Marcelo
Ehrenshaft, Marilyn
Kadiiska, Maria B.
Mason, Ronald P.
Bechara, Etelvino José Henriques [UNIFESP]
dc.subject.por.fl_str_mv Myoglobin
Acetoacetate
2-Methylacetoacetate
Free radicals
Triplet carbonyls
Methylglyoxal
Diacetyl
Ketosis
topic Myoglobin
Acetoacetate
2-Methylacetoacetate
Free radicals
Triplet carbonyls
Methylglyoxal
Diacetyl
Ketosis
description Acetoacetate (AA) and 2-methylacetoacetate (MAA) are accumulated in metabolic disorders such as diabetes and isoleucinemia. Here we examine the mechanism of AA and MAA aerobic oxidation initiated by myoglobin (Mb)/H2O2. We propose a chemiluminescent route involving a dioxetanone intermediate whose thermolysis yields triplet alpha-dicarbonyl species (methylglyoxal and diacetyl). the observed ultraweak chemiluminescence increased linearly on raising the concentration of either Mb (10-500 mu M) or AA (10-100 mM). Oxygen uptake studies revealed that MAA is almost a 100-fold more reactive than AA. EPR spin-trapping studies with MNP/MAA revealed the intermediacy of an alpha-carbon-centered radical and acetyl radical. the latter radical, probably derived from triplet diacetyl, is totally suppressed by sorbate, a well-known quencher of triplet carbonyls. Furthermore, an EPR signal assignable to MNP-AA(center dot) adduct was observed and confirmed by isotope effects. Oxygen consumption and a-dicarbonyl yield were shown to be dependent on AA or MAA concentrations (1-50 mM) and on H2O2 or tert-butOOH added to the Mb-containing reaction mixtures. That ferrylMb is involved in a peroxidase cycle acting on the substrates is suggested by the reaction pH profiles and immunospin-trapping experiments. the generation of radicals and triplet dicarbonyl products by Mb/H2O2/beta-ketoacids may contribute to the adverse health effects of ketogenic unbalance. (C) 2011 Elsevier Inc. All rights reserved.
publishDate 2011
dc.date.none.fl_str_mv 2011-08-01
2016-01-24T14:17:01Z
2016-01-24T14:17:01Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.freeradbiomed.2011.05.002
Free Radical Biology and Medicine. New York: Elsevier B.V., v. 51, n. 3, p. 733-743, 2011.
10.1016/j.freeradbiomed.2011.05.002
WOS000292856900017.pdf
0891-5849
http://repositorio.unifesp.br/handle/11600/33896
WOS:000292856900017
url http://dx.doi.org/10.1016/j.freeradbiomed.2011.05.002
http://repositorio.unifesp.br/handle/11600/33896
identifier_str_mv Free Radical Biology and Medicine. New York: Elsevier B.V., v. 51, n. 3, p. 733-743, 2011.
10.1016/j.freeradbiomed.2011.05.002
WOS000292856900017.pdf
0891-5849
WOS:000292856900017
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Free Radical Biology and Medicine
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
eu_rights_str_mv openAccess
rights_invalid_str_mv http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.format.none.fl_str_mv 733-743
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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