The nature of extra-chromosomal maintenance of transforming plasmids in the filamentous basidiomycete Phanerochaete chrysosporium.
Identifieur interne : 000E43 ( Main/Exploration ); précédent : 000E42; suivant : 000E44The nature of extra-chromosomal maintenance of transforming plasmids in the filamentous basidiomycete Phanerochaete chrysosporium.
Auteurs : T A Randall [États-Unis] ; C A ReddySource :
- Current genetics [ 0172-8083 ] ; 1992.
Descripteurs français
- KwdFr :
- MESH :
- génétique : Basidiomycota, Résistance microbienne aux médicaments.
- métabolisme : Cytosine.
- pharmacologie : Gentamicine.
- physiologie : DNA restriction enzymes, Plasmides, Transformation génétique.
- Méthylation, Vecteurs génétiques.
English descriptors
- KwdEn :
- MESH :
- chemical , metabolism : Cytosine.
- genetics : Basidiomycota, Drug Resistance, Microbial.
- chemical , pharmacology : Gentamicins.
- chemical , physiology : DNA Restriction Enzymes, Plasmids, Transformation, Genetic.
- Genetic Vectors, Methylation.
Abstract
The nature of extra-chromosomal maintenance of the transforming plasmid p12-6 in Phanerochaete chrysosporium was studied. Our results indicate that the plasmid is maintained in the fungal transformants extra-chromosomally as part of a larger endogenous plasmid (designated pME) of P. chrysosporium. Using the total DNA of p12-6 fungal transformants, p12-6, as well as a larger plasmid, p511, were recovered in recA- E. coli strains while only p12-6 was recovered in recA+ E. coli strains. The results also showed that the cytosine methylation system has no apparent effect on the strain-dependent recovery of p12-6 and p511 in E. coli from the total DNA of fungal transformants.
DOI: 10.1007/BF00336850
PubMed: 1314140
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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<term>Cytosine (metabolism)</term>
<term>DNA Restriction Enzymes (physiology)</term>
<term>Drug Resistance, Microbial (genetics)</term>
<term>Genetic Vectors (MeSH)</term>
<term>Gentamicins (pharmacology)</term>
<term>Methylation (MeSH)</term>
<term>Plasmids (physiology)</term>
<term>Transformation, Genetic (physiology)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Basidiomycota (génétique)</term>
<term>Cytosine (métabolisme)</term>
<term>DNA restriction enzymes (physiologie)</term>
<term>Gentamicine (pharmacologie)</term>
<term>Méthylation (MeSH)</term>
<term>Plasmides (physiologie)</term>
<term>Résistance microbienne aux médicaments (génétique)</term>
<term>Transformation génétique (physiologie)</term>
<term>Vecteurs génétiques (MeSH)</term>
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<term>Plasmids</term>
<term>Transformation, Genetic</term>
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<term>Methylation</term>
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<front><div type="abstract" xml:lang="en">The nature of extra-chromosomal maintenance of the transforming plasmid p12-6 in Phanerochaete chrysosporium was studied. Our results indicate that the plasmid is maintained in the fungal transformants extra-chromosomally as part of a larger endogenous plasmid (designated pME) of P. chrysosporium. Using the total DNA of p12-6 fungal transformants, p12-6, as well as a larger plasmid, p511, were recovered in recA- E. coli strains while only p12-6 was recovered in recA+ E. coli strains. The results also showed that the cytosine methylation system has no apparent effect on the strain-dependent recovery of p12-6 and p511 in E. coli from the total DNA of fungal transformants.</div>
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<Abstract><AbstractText>The nature of extra-chromosomal maintenance of the transforming plasmid p12-6 in Phanerochaete chrysosporium was studied. Our results indicate that the plasmid is maintained in the fungal transformants extra-chromosomally as part of a larger endogenous plasmid (designated pME) of P. chrysosporium. Using the total DNA of p12-6 fungal transformants, p12-6, as well as a larger plasmid, p511, were recovered in recA- E. coli strains while only p12-6 was recovered in recA+ E. coli strains. The results also showed that the cytosine methylation system has no apparent effect on the strain-dependent recovery of p12-6 and p511 in E. coli from the total DNA of fungal transformants.</AbstractText>
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