Induction of extracellular hydroxyl radical production by white-rot fungi through quinone redox cycling.
Identifieur interne : 000621 ( Main/Exploration ); précédent : 000620; suivant : 000622Induction of extracellular hydroxyl radical production by white-rot fungi through quinone redox cycling.
Auteurs : Víctor G Mez-Toribio [Espagne] ; Ana B. García-Martín ; María J. Martínez ; Angel T. Martínez ; Francisco GuillénSource :
- Applied and environmental microbiology [ 1098-5336 ] ; 2009.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical , metabolism : Benzoquinones, Edetic Acid, Ferric Compounds, Hydrogen Peroxide, Hydroxyl Radical, Laccase, Oxidoreductases, Peroxidase.
- metabolism : Fungi.
- Oxidation-Reduction.
Abstract
A simple strategy for the induction of extracellular hydroxyl radical (OH) production by white-rot fungi is presented. It involves the incubation of mycelium with quinones and Fe(3+)-EDTA. Succinctly, it is based on the establishment of a quinone redox cycle catalyzed by cell-bound dehydrogenase activities and the ligninolytic enzymes (laccase and peroxidases). The semiquinone intermediate produced by the ligninolytic enzymes drives OH production by a Fenton reaction (H(2)O(2) + Fe(2+) --> OH + OH(-) + Fe(3+)). H(2)O(2) production, Fe(3+) reduction, and OH generation were initially demonstrated with two Pleurotus eryngii mycelia (one producing laccase and versatile peroxidase and the other producing just laccase) and four quinones, 1,4-benzoquinone (BQ), 2-methoxy-1,4-benzoquinone (MBQ), 2,6-dimethoxy-1,4-benzoquinone (DBQ), and 2-methyl-1,4-naphthoquinone (menadione [MD]). In all cases, OH radicals were linearly produced, with the highest rate obtained with MD, followed by DBQ, MBQ, and BQ. These rates correlated with both H(2)O(2) levels and Fe(3+) reduction rates observed with the four quinones. Between the two P. eryngii mycelia used, the best results were obtained with the one producing only laccase, showing higher OH production rates with added purified enzyme. The strategy was then validated in Bjerkandera adusta, Phanerochaete chrysosporium, Phlebia radiata, Pycnoporus cinnabarinus, and Trametes versicolor, also showing good correlation between OH production rates and the kinds and levels of the ligninolytic enzymes expressed by these fungi. We propose this strategy as a useful tool to study the effects of OH radicals on lignin and organopollutant degradation, as well as to improve the bioremediation potential of white-rot fungi.
DOI: 10.1128/AEM.02137-08
PubMed: 19376892
PubMed Central: PMC2698328
Affiliations:
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Martínez</name></author><author><name sortKey="Guillen, Francisco" sort="Guillen, Francisco" uniqKey="Guillen F" first="Francisco" last="Guillén">Francisco Guillén</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2009">2009</date><idno type="RBID">pubmed:19376892</idno><idno type="pmid">19376892</idno><idno type="doi">10.1128/AEM.02137-08</idno><idno type="pmc">PMC2698328</idno><idno type="wicri:Area/Main/Corpus">000630</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">000630</idno><idno type="wicri:Area/Main/Curation">000630</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Curation">000630</idno><idno type="wicri:Area/Main/Exploration">000630</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Induction of extracellular hydroxyl radical production by white-rot fungi through quinone redox cycling.</title><author><name sortKey="G Mez Toribio, Victor" sort="G Mez Toribio, Victor" uniqKey="G Mez Toribio V" first="Víctor" last="G Mez-Toribio">Víctor G Mez-Toribio</name><affiliation wicri:level="3"><nlm:affiliation>Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Madrid, Spain.</nlm:affiliation><country xml:lang="fr">Espagne</country><wicri:regionArea>Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Madrid</wicri:regionArea><placeName><settlement type="city">Madrid</settlement><region nuts="2" type="region">Communauté de Madrid</region></placeName></affiliation></author><author><name sortKey="Garcia Martin, Ana B" sort="Garcia Martin, Ana B" uniqKey="Garcia Martin A" first="Ana B" last="García-Martín">Ana B. García-Martín</name></author><author><name sortKey="Martinez, Maria J" sort="Martinez, Maria J" uniqKey="Martinez M" first="María J" last="Martínez">María J. Martínez</name></author><author><name sortKey="Martinez, Angel T" sort="Martinez, Angel T" uniqKey="Martinez A" first="Angel T" last="Martínez">Angel T. Martínez</name></author><author><name sortKey="Guillen, Francisco" sort="Guillen, Francisco" uniqKey="Guillen F" first="Francisco" last="Guillén">Francisco Guillén</name></author></analytic><series><title level="j">Applied and environmental microbiology</title><idno type="eISSN">1098-5336</idno><imprint><date when="2009" type="published">2009</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Benzoquinones (metabolism)</term><term>Edetic Acid (metabolism)</term><term>Ferric Compounds (metabolism)</term><term>Fungi (metabolism)</term><term>Hydrogen Peroxide (metabolism)</term><term>Hydroxyl Radical (metabolism)</term><term>Laccase (metabolism)</term><term>Oxidation-Reduction (MeSH)</term><term>Oxidoreductases (metabolism)</term><term>Peroxidase (metabolism)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Acide édétique (métabolisme)</term><term>Benzoquinones (métabolisme)</term><term>Champignons (métabolisme)</term><term>Composés du fer III (métabolisme)</term><term>Laccase (métabolisme)</term><term>Myeloperoxidase (métabolisme)</term><term>Oxidoreductases (métabolisme)</term><term>Oxydoréduction (MeSH)</term><term>Peroxyde d'hydrogène (métabolisme)</term><term>Radical hydroxyle (métabolisme)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Benzoquinones</term><term>Edetic Acid</term><term>Ferric Compounds</term><term>Hydrogen Peroxide</term><term>Hydroxyl Radical</term><term>Laccase</term><term>Oxidoreductases</term><term>Peroxidase</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Fungi</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Acide édétique</term><term>Benzoquinones</term><term>Champignons</term><term>Composés du fer III</term><term>Laccase</term><term>Myeloperoxidase</term><term>Oxidoreductases</term><term>Peroxyde d'hydrogène</term><term>Radical hydroxyle</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Oxidation-Reduction</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Oxydoréduction</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">A simple strategy for the induction of extracellular hydroxyl radical (OH) production by white-rot fungi is presented. It involves the incubation of mycelium with quinones and Fe(3+)-EDTA. Succinctly, it is based on the establishment of a quinone redox cycle catalyzed by cell-bound dehydrogenase activities and the ligninolytic enzymes (laccase and peroxidases). The semiquinone intermediate produced by the ligninolytic enzymes drives OH production by a Fenton reaction (H(2)O(2) + Fe(2+) --> OH + OH(-) + Fe(3+)). H(2)O(2) production, Fe(3+) reduction, and OH generation were initially demonstrated with two Pleurotus eryngii mycelia (one producing laccase and versatile peroxidase and the other producing just laccase) and four quinones, 1,4-benzoquinone (BQ), 2-methoxy-1,4-benzoquinone (MBQ), 2,6-dimethoxy-1,4-benzoquinone (DBQ), and 2-methyl-1,4-naphthoquinone (menadione [MD]). In all cases, OH radicals were linearly produced, with the highest rate obtained with MD, followed by DBQ, MBQ, and BQ. These rates correlated with both H(2)O(2) levels and Fe(3+) reduction rates observed with the four quinones. Between the two P. eryngii mycelia used, the best results were obtained with the one producing only laccase, showing higher OH production rates with added purified enzyme. The strategy was then validated in Bjerkandera adusta, Phanerochaete chrysosporium, Phlebia radiata, Pycnoporus cinnabarinus, and Trametes versicolor, also showing good correlation between OH production rates and the kinds and levels of the ligninolytic enzymes expressed by these fungi. We propose this strategy as a useful tool to study the effects of OH radicals on lignin and organopollutant degradation, as well as to improve the bioremediation potential of white-rot fungi.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">19376892</PMID><DateCompleted><Year>2009</Year><Month>06</Month><Day>25</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1098-5336</ISSN><JournalIssue CitedMedium="Internet"><Volume>75</Volume><Issue>12</Issue><PubDate><Year>2009</Year><Month>Jun</Month></PubDate></JournalIssue><Title>Applied and environmental microbiology</Title><ISOAbbreviation>Appl Environ Microbiol</ISOAbbreviation></Journal><ArticleTitle>Induction of extracellular hydroxyl radical production by white-rot fungi through quinone redox cycling.</ArticleTitle><Pagination><MedlinePgn>3944-53</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1128/AEM.02137-08</ELocationID><Abstract><AbstractText>A simple strategy for the induction of extracellular hydroxyl radical (OH) production by white-rot fungi is presented. It involves the incubation of mycelium with quinones and Fe(3+)-EDTA. Succinctly, it is based on the establishment of a quinone redox cycle catalyzed by cell-bound dehydrogenase activities and the ligninolytic enzymes (laccase and peroxidases). The semiquinone intermediate produced by the ligninolytic enzymes drives OH production by a Fenton reaction (H(2)O(2) + Fe(2+) --> OH + OH(-) + Fe(3+)). H(2)O(2) production, Fe(3+) reduction, and OH generation were initially demonstrated with two Pleurotus eryngii mycelia (one producing laccase and versatile peroxidase and the other producing just laccase) and four quinones, 1,4-benzoquinone (BQ), 2-methoxy-1,4-benzoquinone (MBQ), 2,6-dimethoxy-1,4-benzoquinone (DBQ), and 2-methyl-1,4-naphthoquinone (menadione [MD]). In all cases, OH radicals were linearly produced, with the highest rate obtained with MD, followed by DBQ, MBQ, and BQ. These rates correlated with both H(2)O(2) levels and Fe(3+) reduction rates observed with the four quinones. Between the two P. eryngii mycelia used, the best results were obtained with the one producing only laccase, showing higher OH production rates with added purified enzyme. The strategy was then validated in Bjerkandera adusta, Phanerochaete chrysosporium, Phlebia radiata, Pycnoporus cinnabarinus, and Trametes versicolor, also showing good correlation between OH production rates and the kinds and levels of the ligninolytic enzymes expressed by these fungi. We propose this strategy as a useful tool to study the effects of OH radicals on lignin and organopollutant degradation, as well as to improve the bioremediation potential of white-rot fungi.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Gómez-Toribio</LastName><ForeName>Víctor</ForeName><Initials>V</Initials><AffiliationInfo><Affiliation>Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Madrid, Spain.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>García-Martín</LastName><ForeName>Ana B</ForeName><Initials>AB</Initials></Author><Author ValidYN="Y"><LastName>Martínez</LastName><ForeName>María J</ForeName><Initials>MJ</Initials></Author><Author ValidYN="Y"><LastName>Martínez</LastName><ForeName>Angel T</ForeName><Initials>AT</Initials></Author><Author ValidYN="Y"><LastName>Guillén</LastName><ForeName>Francisco</ForeName><Initials>F</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2009</Year><Month>04</Month><Day>17</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Appl Environ Microbiol</MedlineTA><NlmUniqueID>7605801</NlmUniqueID><ISSNLinking>0099-2240</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D016227">Benzoquinones</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D005290">Ferric Compounds</NameOfSubstance></Chemical><Chemical><RegistryNumber>3352-57-6</RegistryNumber><NameOfSubstance UI="D017665">Hydroxyl 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MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D042845" MajorTopicYN="N">Laccase</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010084" MajorTopicYN="N">Oxidation-Reduction</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010088" MajorTopicYN="N">Oxidoreductases</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D009195" MajorTopicYN="N">Peroxidase</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2009</Year><Month>4</Month><Day>21</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate 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García-Martín</name><name sortKey="Guillen, Francisco" sort="Guillen, Francisco" uniqKey="Guillen F" first="Francisco" last="Guillén">Francisco Guillén</name><name sortKey="Martinez, Angel T" sort="Martinez, Angel T" uniqKey="Martinez A" first="Angel T" last="Martínez">Angel T. Martínez</name><name sortKey="Martinez, Maria J" sort="Martinez, Maria J" uniqKey="Martinez M" first="María J" last="Martínez">María J. Martínez</name></noCountry><country name="Espagne"><region name="Communauté de Madrid"><name sortKey="G Mez Toribio, Victor" sort="G Mez Toribio, Victor" uniqKey="G Mez Toribio V" first="Víctor" last="G Mez-Toribio">Víctor G Mez-Toribio</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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