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Cloning, sequencing, and heterologous expression of a cellulase-encoding cDNA (cbh1) from Penicillium janthinellum.

Identifieur interne : 000E33 ( Main/Exploration ); précédent : 000E32; suivant : 000E34

Cloning, sequencing, and heterologous expression of a cellulase-encoding cDNA (cbh1) from Penicillium janthinellum.

Auteurs : A. Koch [Allemagne] ; C T Weigel ; G. Schulz

Source :

RBID : pubmed:8440481

Descripteurs français

English descriptors

Abstract

From a Penicillium janthinellum cDNA library, two clones with 1.8- and 1.9-kb inserts were isolated by hybridization to a Trichoderma reesei cellulase-encoding gene probe (egl1). Both cDNAs have identical 5' ends and coding sequences, but different polyadenylation start points in their 3' untranslated regions. In the nucleotide (nt) sequence, one open reading frame of 537 amino acids was detected which shows 56% homology with endoglucanase I of T. reesei and 70% homology with cellobiohydrolase I of T. reesei, Phanerochaete chrysosporium, and Humicola grisea. Expression of the 1.9-kb cDNA in the Escherichia coli T7 system led to the detection of a 57-kDa protein, in agreement with the theoretical value. Fusion to the promoter of the yeast phosphoglycerokinase-encoding gene led to efficient expression and partial secretion of the cDNA-encoded cellulase with cellobiohydrolase I activity in Saccharomyces cerevisiae.

DOI: 10.1016/0378-1119(93)90761-q
PubMed: 8440481


Affiliations:


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Le document en format XML

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<title xml:lang="en">Cloning, sequencing, and heterologous expression of a cellulase-encoding cDNA (cbh1) from Penicillium janthinellum.</title>
<author>
<name sortKey="Koch, A" sort="Koch, A" uniqKey="Koch A" first="A" last="Koch">A. Koch</name>
<affiliation wicri:level="1">
<nlm:affiliation>Institut für Mikrobiologie, Humboldt-Universität zu Berlin, Kleinmachnow, Germany.</nlm:affiliation>
<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Institut für Mikrobiologie, Humboldt-Universität zu Berlin, Kleinmachnow</wicri:regionArea>
<wicri:noRegion>Kleinmachnow</wicri:noRegion>
<wicri:noRegion>Kleinmachnow</wicri:noRegion>
<wicri:noRegion>Kleinmachnow</wicri:noRegion>
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<author>
<name sortKey="Weigel, C T" sort="Weigel, C T" uniqKey="Weigel C" first="C T" last="Weigel">C T Weigel</name>
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<author>
<name sortKey="Schulz, G" sort="Schulz, G" uniqKey="Schulz G" first="G" last="Schulz">G. Schulz</name>
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<term>Agaricales (enzymology)</term>
<term>Agaricales (genetics)</term>
<term>Amino Acid Sequence (MeSH)</term>
<term>Bacteriophage T7 (genetics)</term>
<term>Base Sequence (MeSH)</term>
<term>Cellulase (genetics)</term>
<term>Cloning, Molecular (MeSH)</term>
<term>DNA, Fungal (genetics)</term>
<term>Escherichia coli (genetics)</term>
<term>Genes, Fungal (MeSH)</term>
<term>Mitosporic Fungi (enzymology)</term>
<term>Mitosporic Fungi (genetics)</term>
<term>Molecular Sequence Data (MeSH)</term>
<term>Penicillium (enzymology)</term>
<term>Penicillium (genetics)</term>
<term>Saccharomyces cerevisiae (enzymology)</term>
<term>Saccharomyces cerevisiae (genetics)</term>
<term>Sequence Homology, Amino Acid (MeSH)</term>
<term>Sequence Homology, Nucleic Acid (MeSH)</term>
<term>Trichoderma (enzymology)</term>
<term>Trichoderma (genetics)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>ADN fongique (génétique)</term>
<term>Agaricales (enzymologie)</term>
<term>Agaricales (génétique)</term>
<term>Bactériophage T7 (génétique)</term>
<term>Cellulase (génétique)</term>
<term>Clonage moléculaire (MeSH)</term>
<term>Deuteromycota (enzymologie)</term>
<term>Deuteromycota (génétique)</term>
<term>Données de séquences moléculaires (MeSH)</term>
<term>Escherichia coli (génétique)</term>
<term>Gènes fongiques (MeSH)</term>
<term>Penicillium (enzymologie)</term>
<term>Penicillium (génétique)</term>
<term>Saccharomyces cerevisiae (enzymologie)</term>
<term>Saccharomyces cerevisiae (génétique)</term>
<term>Similitude de séquences d'acides aminés (MeSH)</term>
<term>Similitude de séquences d'acides nucléiques (MeSH)</term>
<term>Séquence d'acides aminés (MeSH)</term>
<term>Séquence nucléotidique (MeSH)</term>
<term>Trichoderma (enzymologie)</term>
<term>Trichoderma (génétique)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Cellulase</term>
<term>DNA, Fungal</term>
</keywords>
<keywords scheme="MESH" qualifier="enzymologie" xml:lang="fr">
<term>Agaricales</term>
<term>Deuteromycota</term>
<term>Penicillium</term>
<term>Saccharomyces cerevisiae</term>
<term>Trichoderma</term>
</keywords>
<keywords scheme="MESH" qualifier="enzymology" xml:lang="en">
<term>Agaricales</term>
<term>Mitosporic Fungi</term>
<term>Penicillium</term>
<term>Saccharomyces cerevisiae</term>
<term>Trichoderma</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Agaricales</term>
<term>Bacteriophage T7</term>
<term>Escherichia coli</term>
<term>Mitosporic Fungi</term>
<term>Penicillium</term>
<term>Saccharomyces cerevisiae</term>
<term>Trichoderma</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>ADN fongique</term>
<term>Agaricales</term>
<term>Bactériophage T7</term>
<term>Cellulase</term>
<term>Deuteromycota</term>
<term>Escherichia coli</term>
<term>Penicillium</term>
<term>Saccharomyces cerevisiae</term>
<term>Trichoderma</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Amino Acid Sequence</term>
<term>Base Sequence</term>
<term>Cloning, Molecular</term>
<term>Genes, Fungal</term>
<term>Molecular Sequence Data</term>
<term>Sequence Homology, Amino Acid</term>
<term>Sequence Homology, Nucleic Acid</term>
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<term>Clonage moléculaire</term>
<term>Données de séquences moléculaires</term>
<term>Gènes fongiques</term>
<term>Similitude de séquences d'acides aminés</term>
<term>Similitude de séquences d'acides nucléiques</term>
<term>Séquence d'acides aminés</term>
<term>Séquence nucléotidique</term>
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<front>
<div type="abstract" xml:lang="en">From a Penicillium janthinellum cDNA library, two clones with 1.8- and 1.9-kb inserts were isolated by hybridization to a Trichoderma reesei cellulase-encoding gene probe (egl1). Both cDNAs have identical 5' ends and coding sequences, but different polyadenylation start points in their 3' untranslated regions. In the nucleotide (nt) sequence, one open reading frame of 537 amino acids was detected which shows 56% homology with endoglucanase I of T. reesei and 70% homology with cellobiohydrolase I of T. reesei, Phanerochaete chrysosporium, and Humicola grisea. Expression of the 1.9-kb cDNA in the Escherichia coli T7 system led to the detection of a 57-kDa protein, in agreement with the theoretical value. Fusion to the promoter of the yeast phosphoglycerokinase-encoding gene led to efficient expression and partial secretion of the cDNA-encoded cellulase with cellobiohydrolase I activity in Saccharomyces cerevisiae.</div>
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<DateCompleted>
<Year>1993</Year>
<Month>03</Month>
<Day>30</Day>
</DateCompleted>
<DateRevised>
<Year>2019</Year>
<Month>07</Month>
<Day>07</Day>
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<ISSN IssnType="Print">0378-1119</ISSN>
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<Volume>124</Volume>
<Issue>1</Issue>
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<Year>1993</Year>
<Month>Feb</Month>
<Day>14</Day>
</PubDate>
</JournalIssue>
<Title>Gene</Title>
<ISOAbbreviation>Gene</ISOAbbreviation>
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<ArticleTitle>Cloning, sequencing, and heterologous expression of a cellulase-encoding cDNA (cbh1) from Penicillium janthinellum.</ArticleTitle>
<Pagination>
<MedlinePgn>57-65</MedlinePgn>
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<Abstract>
<AbstractText>From a Penicillium janthinellum cDNA library, two clones with 1.8- and 1.9-kb inserts were isolated by hybridization to a Trichoderma reesei cellulase-encoding gene probe (egl1). Both cDNAs have identical 5' ends and coding sequences, but different polyadenylation start points in their 3' untranslated regions. In the nucleotide (nt) sequence, one open reading frame of 537 amino acids was detected which shows 56% homology with endoglucanase I of T. reesei and 70% homology with cellobiohydrolase I of T. reesei, Phanerochaete chrysosporium, and Humicola grisea. Expression of the 1.9-kb cDNA in the Escherichia coli T7 system led to the detection of a 57-kDa protein, in agreement with the theoretical value. Fusion to the promoter of the yeast phosphoglycerokinase-encoding gene led to efficient expression and partial secretion of the cDNA-encoded cellulase with cellobiohydrolase I activity in Saccharomyces cerevisiae.</AbstractText>
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<AccessionNumber>L03654</AccessionNumber>
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<AccessionNumber>X65067</AccessionNumber>
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<DescriptorName UI="D000363" MajorTopicYN="N">Agaricales</DescriptorName>
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<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
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<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
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<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
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<li>Allemagne</li>
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