Serveur d'exploration sur le phanerochaete

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Truncated-gene reporter system for studying the regulation of manganese peroxidase expression.

Identifieur interne : 000B93 ( Main/Exploration ); précédent : 000B92; suivant : 000B94

Truncated-gene reporter system for studying the regulation of manganese peroxidase expression.

Auteurs : J M Gettemy [États-Unis] ; D. Li ; M. Alic ; M H Gold

Source :

RBID : pubmed:9211796

Descripteurs français

English descriptors

Abstract

The expression of manganese peroxidase (MnP) in nitrogen-limited cultures of Phanerochaete chrysosporium is regulated by Mn, heat shock (HS), and H2O2 at the level of gene transcription. We have constructed a homologous gene reporter system to further examine the regulation of two mnp genes, mnp1 and mnp2, encoding individual MnP isozymes. Internal deletions of 234 and 359 bp were made within the coding regions of the mnp1 and mnp2 genes, respectively. The truncated mnp genes were subcloned into the shuttle vector pOGI18, which includes the Schizophylum commune ade5 gene as a selectable marker, and transformed into a P. chrysosporium Ade1 auxotrophic mutant. Northern-blot analysis of purified Ade+ transformants demonstrated that both of the truncated mnp genes were regulated in a manner similar to the endogenous mnp genes with respect to nitrogen limitation and induction by Mn, HS, and H2O2.

DOI: 10.1007/s002940050239
PubMed: 9211796


Affiliations:


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Le document en format XML

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<title xml:lang="en">Truncated-gene reporter system for studying the regulation of manganese peroxidase expression.</title>
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<nlm:affiliation>Department of Biochemistry and Molecular Biology, Oregon Graduate Institute of Science and Technology, P.O. Box 91000, Portland, OR 97291-1000, USA.</nlm:affiliation>
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<name sortKey="Gold, M H" sort="Gold, M H" uniqKey="Gold M" first="M H" last="Gold">M H Gold</name>
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<term>Enzyme Activation (MeSH)</term>
<term>Gene Expression Regulation, Fungal (MeSH)</term>
<term>Genes, Reporter (MeSH)</term>
<term>Hot Temperature (MeSH)</term>
<term>Hydrogen Peroxide (metabolism)</term>
<term>Hydrogen Sulfide (metabolism)</term>
<term>Isoenzymes (MeSH)</term>
<term>Manganese (metabolism)</term>
<term>Manganese (pharmacology)</term>
<term>Nitrogen (metabolism)</term>
<term>Peroxidases (drug effects)</term>
<term>Peroxidases (genetics)</term>
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<term>Activation enzymatique (MeSH)</term>
<term>Azote (métabolisme)</term>
<term>Basidiomycota (génétique)</term>
<term>Basidiomycota (métabolisme)</term>
<term>Gènes rapporteurs (MeSH)</term>
<term>Isoenzymes (MeSH)</term>
<term>Manganèse (métabolisme)</term>
<term>Manganèse (pharmacologie)</term>
<term>Peroxidases (effets des médicaments et des substances chimiques)</term>
<term>Peroxidases (génétique)</term>
<term>Peroxidases (métabolisme)</term>
<term>Peroxyde d'hydrogène (métabolisme)</term>
<term>Protéines recombinantes (génétique)</term>
<term>Protéines recombinantes (métabolisme)</term>
<term>Régulation de l'expression des gènes fongiques (MeSH)</term>
<term>Sulfure d'hydrogène (métabolisme)</term>
<term>Température élevée (MeSH)</term>
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<term>Peroxidases</term>
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<term>Hydrogen Peroxide</term>
<term>Hydrogen Sulfide</term>
<term>Manganese</term>
<term>Nitrogen</term>
<term>Peroxidases</term>
<term>Recombinant Proteins</term>
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<term>Basidiomycota</term>
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<term>Peroxidases</term>
<term>Protéines recombinantes</term>
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<term>Basidiomycota</term>
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<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Azote</term>
<term>Basidiomycota</term>
<term>Manganèse</term>
<term>Peroxidases</term>
<term>Peroxyde d'hydrogène</term>
<term>Protéines recombinantes</term>
<term>Sulfure d'hydrogène</term>
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<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr">
<term>Manganèse</term>
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<term>Manganese</term>
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<term>Enzyme Activation</term>
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<term>Gènes rapporteurs</term>
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<div type="abstract" xml:lang="en">The expression of manganese peroxidase (MnP) in nitrogen-limited cultures of Phanerochaete chrysosporium is regulated by Mn, heat shock (HS), and H2O2 at the level of gene transcription. We have constructed a homologous gene reporter system to further examine the regulation of two mnp genes, mnp1 and mnp2, encoding individual MnP isozymes. Internal deletions of 234 and 359 bp were made within the coding regions of the mnp1 and mnp2 genes, respectively. The truncated mnp genes were subcloned into the shuttle vector pOGI18, which includes the Schizophylum commune ade5 gene as a selectable marker, and transformed into a P. chrysosporium Ade1 auxotrophic mutant. Northern-blot analysis of purified Ade+ transformants demonstrated that both of the truncated mnp genes were regulated in a manner similar to the endogenous mnp genes with respect to nitrogen limitation and induction by Mn, HS, and H2O2.</div>
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