Serveur d'exploration sur le phanerochaete

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Heterologous expression of endo-1,4-beta-xylanaseC from Phanerochaete chrysosporium in Pichia pastoris.

Identifieur interne : 000505 ( Main/Exploration ); précédent : 000504; suivant : 000506

Heterologous expression of endo-1,4-beta-xylanaseC from Phanerochaete chrysosporium in Pichia pastoris.

Auteurs : Nguyen Duc Huy [Corée du Sud] ; Seung-Wook Kim ; Seung-Moon Park

Source :

RBID : pubmed:21393056

Descripteurs français

English descriptors

Abstract

The cDNA of endo-1,4-β-xylanaseC, isolated from Phanerochaete chrysosporium, was expressed in Pichia pastoris, under the control of the alcohol oxidase I promoter. Using either the intrinsic leader peptide of xylanaseC or the α-factor signal peptide of Saccharomyces cerevisiae, xylanaseC is efficiently secreted into the medium, at a maximum concentration of 2500 U·l(-1).

DOI: 10.1016/j.jbiosc.2011.02.010
PubMed: 21393056


Affiliations:


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Le document en format XML

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<name sortKey="Huy, Nguyen Duc" sort="Huy, Nguyen Duc" uniqKey="Huy N" first="Nguyen Duc" last="Huy">Nguyen Duc Huy</name>
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<nlm:affiliation>Division of Biotechnology, College of Environmental and Bioresource Sciences, Chonbuk National University, Iksan 570-752, Republic of Korea.</nlm:affiliation>
<country xml:lang="fr">Corée du Sud</country>
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<name sortKey="Kim, Seung Wook" sort="Kim, Seung Wook" uniqKey="Kim S" first="Seung-Wook" last="Kim">Seung-Wook Kim</name>
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<name sortKey="Park, Seung Moon" sort="Park, Seung Moon" uniqKey="Park S" first="Seung-Moon" last="Park">Seung-Moon Park</name>
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<term>Cloning, Molecular (MeSH)</term>
<term>Culture Media (chemistry)</term>
<term>Endo-1,4-beta Xylanases (biosynthesis)</term>
<term>Fungal Proteins (biosynthesis)</term>
<term>Genetic Vectors (MeSH)</term>
<term>Industrial Microbiology (MeSH)</term>
<term>Molecular Weight (MeSH)</term>
<term>Phanerochaete (enzymology)</term>
<term>Phanerochaete (genetics)</term>
<term>Pichia (metabolism)</term>
<term>Promoter Regions, Genetic (MeSH)</term>
<term>Protein Sorting Signals (MeSH)</term>
<term>Recombinant Proteins (biosynthesis)</term>
<term>Saccharomyces cerevisiae (genetics)</term>
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<term>Clonage moléculaire (MeSH)</term>
<term>Endo-1,4-beta xylanases (biosynthèse)</term>
<term>Masse moléculaire (MeSH)</term>
<term>Microbiologie industrielle (MeSH)</term>
<term>Milieux de culture (composition chimique)</term>
<term>Phanerochaete (enzymologie)</term>
<term>Phanerochaete (génétique)</term>
<term>Pichia (métabolisme)</term>
<term>Protéines fongiques (biosynthèse)</term>
<term>Protéines recombinantes (biosynthèse)</term>
<term>Régions promotrices (génétique) (MeSH)</term>
<term>Saccharomyces cerevisiae (génétique)</term>
<term>Signaux de triage des protéines (MeSH)</term>
<term>Vecteurs génétiques (MeSH)</term>
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<keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en">
<term>Endo-1,4-beta Xylanases</term>
<term>Fungal Proteins</term>
<term>Recombinant Proteins</term>
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<term>Culture Media</term>
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<keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr">
<term>Endo-1,4-beta xylanases</term>
<term>Protéines fongiques</term>
<term>Protéines recombinantes</term>
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<term>Milieux de culture</term>
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<term>Industrial Microbiology</term>
<term>Molecular Weight</term>
<term>Promoter Regions, Genetic</term>
<term>Protein Sorting Signals</term>
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<term>Masse moléculaire</term>
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<div type="abstract" xml:lang="en">The cDNA of endo-1,4-β-xylanaseC, isolated from Phanerochaete chrysosporium, was expressed in Pichia pastoris, under the control of the alcohol oxidase I promoter. Using either the intrinsic leader peptide of xylanaseC or the α-factor signal peptide of Saccharomyces cerevisiae, xylanaseC is efficiently secreted into the medium, at a maximum concentration of 2500 U·l(-1).</div>
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