Serveur d'exploration sur le phanerochaete

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Heterologous expression of manganese peroxidase in Aspergillus niger and its effect on phenanthrene removal from soil.

Identifieur interne : 000504 ( Main/Exploration ); précédent : 000503; suivant : 000505

Heterologous expression of manganese peroxidase in Aspergillus niger and its effect on phenanthrene removal from soil.

Auteurs : Diana V. Cortés-Espinosa [Mexique] ; Ángel E. Absal N ; Noé Sanchez ; Octavio Loera ; Refugio Rodríguez-Vázquez ; Francisco J. Fernández

Source :

RBID : pubmed:22286039

Descripteurs français

English descriptors

Abstract

A strain of Aspergillus niger, previously isolated from sugarcane bagasse because of its capacity to degrade phenanthrene in soil by solid culture, was used to express a manganese peroxidase gene (mnp1) from Phanerochaete chrysosporium, aiming at increasing its polycyclic aromatic hydrocarbons degradation capacity. Transformants were selected based on their resistance to hygromycin B and the discoloration induced on Poly R-478 dye by the peroxidase activity. The recombinant A. niger SBC2-T3 strain developed MnP activity and was able to remove 95% of the initial phenanthrene (400 ppm) from a microcosm soil system after 17 days, whereas the wild strain removed 72% under the same conditions. Transformation success was confirmed by PCR amplification using gene-specific primers, and a single fragment (1,348 bp long, as expected) of the recombinant mnp1 was amplified in the DNA from transformants, which was absent from the parental strain.

DOI: 10.1159/000331563
PubMed: 22286039


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Le document en format XML

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<term>Aspergillus niger (enzymology)</term>
<term>Aspergillus niger (genetics)</term>
<term>Aspergillus niger (metabolism)</term>
<term>Biotransformation (MeSH)</term>
<term>DNA Primers (genetics)</term>
<term>DNA, Fungal (genetics)</term>
<term>Peroxidases (genetics)</term>
<term>Peroxidases (metabolism)</term>
<term>Phanerochaete (enzymology)</term>
<term>Phanerochaete (genetics)</term>
<term>Phenanthrenes (metabolism)</term>
<term>Polymerase Chain Reaction (MeSH)</term>
<term>Recombinant Proteins (genetics)</term>
<term>Recombinant Proteins (metabolism)</term>
<term>Selection, Genetic (MeSH)</term>
<term>Soil Pollutants (metabolism)</term>
<term>Time Factors (MeSH)</term>
<term>Transformation, Genetic (MeSH)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>ADN fongique (génétique)</term>
<term>Amorces ADN (génétique)</term>
<term>Aspergillus niger (enzymologie)</term>
<term>Aspergillus niger (génétique)</term>
<term>Aspergillus niger (métabolisme)</term>
<term>Biotransformation (MeSH)</term>
<term>Facteurs temps (MeSH)</term>
<term>Peroxidases (génétique)</term>
<term>Peroxidases (métabolisme)</term>
<term>Phanerochaete (enzymologie)</term>
<term>Phanerochaete (génétique)</term>
<term>Phénanthrènes (métabolisme)</term>
<term>Polluants du sol (métabolisme)</term>
<term>Protéines recombinantes (génétique)</term>
<term>Protéines recombinantes (métabolisme)</term>
<term>Réaction de polymérisation en chaîne (MeSH)</term>
<term>Sélection génétique (MeSH)</term>
<term>Transformation génétique (MeSH)</term>
</keywords>
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<term>DNA Primers</term>
<term>DNA, Fungal</term>
<term>Peroxidases</term>
<term>Recombinant Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="enzymologie" xml:lang="fr">
<term>Aspergillus niger</term>
<term>Phanerochaete</term>
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<keywords scheme="MESH" qualifier="enzymology" xml:lang="en">
<term>Aspergillus niger</term>
<term>Phanerochaete</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Aspergillus niger</term>
<term>Phanerochaete</term>
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<term>ADN fongique</term>
<term>Amorces ADN</term>
<term>Aspergillus niger</term>
<term>Peroxidases</term>
<term>Phanerochaete</term>
<term>Protéines recombinantes</term>
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<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Aspergillus niger</term>
<term>Peroxidases</term>
<term>Phenanthrenes</term>
<term>Recombinant Proteins</term>
<term>Soil Pollutants</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Aspergillus niger</term>
<term>Peroxidases</term>
<term>Phénanthrènes</term>
<term>Polluants du sol</term>
<term>Protéines recombinantes</term>
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<term>Polymerase Chain Reaction</term>
<term>Selection, Genetic</term>
<term>Time Factors</term>
<term>Transformation, Genetic</term>
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<term>Biotransformation</term>
<term>Facteurs temps</term>
<term>Réaction de polymérisation en chaîne</term>
<term>Sélection génétique</term>
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<div type="abstract" xml:lang="en">A strain of Aspergillus niger, previously isolated from sugarcane bagasse because of its capacity to degrade phenanthrene in soil by solid culture, was used to express a manganese peroxidase gene (mnp1) from Phanerochaete chrysosporium, aiming at increasing its polycyclic aromatic hydrocarbons degradation capacity. Transformants were selected based on their resistance to hygromycin B and the discoloration induced on Poly R-478 dye by the peroxidase activity. The recombinant A. niger SBC2-T3 strain developed MnP activity and was able to remove 95% of the initial phenanthrene (400 ppm) from a microcosm soil system after 17 days, whereas the wild strain removed 72% under the same conditions. Transformation success was confirmed by PCR amplification using gene-specific primers, and a single fragment (1,348 bp long, as expected) of the recombinant mnp1 was amplified in the DNA from transformants, which was absent from the parental strain.</div>
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<AbstractText>A strain of Aspergillus niger, previously isolated from sugarcane bagasse because of its capacity to degrade phenanthrene in soil by solid culture, was used to express a manganese peroxidase gene (mnp1) from Phanerochaete chrysosporium, aiming at increasing its polycyclic aromatic hydrocarbons degradation capacity. Transformants were selected based on their resistance to hygromycin B and the discoloration induced on Poly R-478 dye by the peroxidase activity. The recombinant A. niger SBC2-T3 strain developed MnP activity and was able to remove 95% of the initial phenanthrene (400 ppm) from a microcosm soil system after 17 days, whereas the wild strain removed 72% under the same conditions. Transformation success was confirmed by PCR amplification using gene-specific primers, and a single fragment (1,348 bp long, as expected) of the recombinant mnp1 was amplified in the DNA from transformants, which was absent from the parental strain.</AbstractText>
<CopyrightInformation>Copyright © 2012 S. Karger AG, Basel.</CopyrightInformation>
</Abstract>
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<LastName>Cortés-Espinosa</LastName>
<ForeName>Diana V</ForeName>
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<Affiliation>Centro de Investigación en Biotecnologóa Aplicada del IPN, Carretera Federal Santa Inés, Tepetitla de Lardizabal, Mexico.</Affiliation>
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<LastName>Absalón</LastName>
<ForeName>Ángel E</ForeName>
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<LastName>Sanchez</LastName>
<ForeName>Noé</ForeName>
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<LastName>Loera</LastName>
<ForeName>Octavio</ForeName>
<Initials>O</Initials>
</Author>
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<LastName>Rodríguez-Vázquez</LastName>
<ForeName>Refugio</ForeName>
<Initials>R</Initials>
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<Author ValidYN="Y">
<LastName>Fernández</LastName>
<ForeName>Francisco J</ForeName>
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<Country>Switzerland</Country>
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<DescriptorName UI="D001234" MajorTopicYN="N">Aspergillus niger</DescriptorName>
<QualifierName UI="Q000201" MajorTopicYN="Y">enzymology</QualifierName>
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