Serveur d'exploration sur le phanerochaete

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Glutathione-mediated mineralization of 14C-labeled 2-amino-4,6-dinitrotoluene by manganese-dependent peroxidase H5 from the white-rot fungus Phanerochaete chrysosporium.

Identifieur interne : 000A81 ( Main/Exploration ); précédent : 000A80; suivant : 000A82

Glutathione-mediated mineralization of 14C-labeled 2-amino-4,6-dinitrotoluene by manganese-dependent peroxidase H5 from the white-rot fungus Phanerochaete chrysosporium.

Auteurs : B. Van Aken [Belgique] ; M D Cameron ; J D Stahl ; A. Plumat ; H. Naveau ; S D Aust ; S N Agathos

Source :

RBID : pubmed:11131391

Descripteurs français

English descriptors

Abstract

Manganese-dependent peroxidase (MnP) H5 from the white-rot fungus Phanerochaete chrysosporium, in the presence of either Mn(II) (10 mM) or GSH (10 mM). was able to mineralize 14C-U-ring-labeled 2-amino-4,6-dinitrotoluene (2-A-4,6-DNT) up to 29% in 12 days. When both Mn(II) and GSH were present, the mineralization extent reached 82%. On the other hand, no significant mineralization was observed in the absence of both Mn(II) and GSH, suggesting the requirement of a mediator [either Mn(II) or GSH] for the degradation of 2-A-4,6-DNT by MnP. Using electron spin resonance (ESR) techniques, it was found that the glutathionyl free radical (GS*) was produced through the oxidation of GSH by MnP in the presence as well as in the absence of Mn(II). GS* was also generated through the direct oxidation of GSH by Mn(III). Our results strongly suggest the involvement of GS* in the GSH-mediated mineralization of 2-A-4,6-DNT by MnP.

DOI: 10.1007/s002530000436
PubMed: 11131391


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Le document en format XML

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<term>Aniline Compounds (metabolism)</term>
<term>Biodegradation, Environmental (MeSH)</term>
<term>Electron Spin Resonance Spectroscopy (MeSH)</term>
<term>Free Radicals (MeSH)</term>
<term>Glutathione (metabolism)</term>
<term>Manganese (metabolism)</term>
<term>Oxidation-Reduction (MeSH)</term>
<term>Peroxidases (metabolism)</term>
<term>Phanerochaete (enzymology)</term>
<term>Spin Labels (MeSH)</term>
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<term>Dépollution biologique de l'environnement (MeSH)</term>
<term>Dérivés de l'aniline (métabolisme)</term>
<term>Glutathion (métabolisme)</term>
<term>Manganèse (métabolisme)</term>
<term>Marqueurs de spin (MeSH)</term>
<term>Oxydoréduction (MeSH)</term>
<term>Peroxidases (métabolisme)</term>
<term>Phanerochaete (enzymologie)</term>
<term>Radicaux libres (MeSH)</term>
<term>Spectroscopie de résonance de spin électronique (MeSH)</term>
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<term>Aniline Compounds</term>
<term>Glutathione</term>
<term>Manganese</term>
<term>Peroxidases</term>
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<term>Phanerochaete</term>
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<term>Phanerochaete</term>
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<term>Dérivés de l'aniline</term>
<term>Glutathion</term>
<term>Manganèse</term>
<term>Peroxidases</term>
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<term>Biodegradation, Environmental</term>
<term>Electron Spin Resonance Spectroscopy</term>
<term>Free Radicals</term>
<term>Oxidation-Reduction</term>
<term>Spin Labels</term>
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<term>Dépollution biologique de l'environnement</term>
<term>Marqueurs de spin</term>
<term>Oxydoréduction</term>
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<div type="abstract" xml:lang="en">Manganese-dependent peroxidase (MnP) H5 from the white-rot fungus Phanerochaete chrysosporium, in the presence of either Mn(II) (10 mM) or GSH (10 mM). was able to mineralize 14C-U-ring-labeled 2-amino-4,6-dinitrotoluene (2-A-4,6-DNT) up to 29% in 12 days. When both Mn(II) and GSH were present, the mineralization extent reached 82%. On the other hand, no significant mineralization was observed in the absence of both Mn(II) and GSH, suggesting the requirement of a mediator [either Mn(II) or GSH] for the degradation of 2-A-4,6-DNT by MnP. Using electron spin resonance (ESR) techniques, it was found that the glutathionyl free radical (GS*) was produced through the oxidation of GSH by MnP in the presence as well as in the absence of Mn(II). GS* was also generated through the direct oxidation of GSH by Mn(III). Our results strongly suggest the involvement of GS* in the GSH-mediated mineralization of 2-A-4,6-DNT by MnP.</div>
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<AbstractText>Manganese-dependent peroxidase (MnP) H5 from the white-rot fungus Phanerochaete chrysosporium, in the presence of either Mn(II) (10 mM) or GSH (10 mM). was able to mineralize 14C-U-ring-labeled 2-amino-4,6-dinitrotoluene (2-A-4,6-DNT) up to 29% in 12 days. When both Mn(II) and GSH were present, the mineralization extent reached 82%. On the other hand, no significant mineralization was observed in the absence of both Mn(II) and GSH, suggesting the requirement of a mediator [either Mn(II) or GSH] for the degradation of 2-A-4,6-DNT by MnP. Using electron spin resonance (ESR) techniques, it was found that the glutathionyl free radical (GS*) was produced through the oxidation of GSH by MnP in the presence as well as in the absence of Mn(II). GS* was also generated through the direct oxidation of GSH by Mn(III). Our results strongly suggest the involvement of GS* in the GSH-mediated mineralization of 2-A-4,6-DNT by MnP.</AbstractText>
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