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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1984-2-14
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pubmed:abstractText |
Several plasmid vectors for cloning in Staphylococcus aureus and S. carnosus have been constructed and characterized. The chimeric plasmids are composed of parts of the following parental plasmids: The chloramphenicol-resistance plasmid, pC194, the tetracycline-resistance plasmid, pMK148, and the erythromycin-resistance plasmid, pE12. All the chimeric plasmids confer two selectable antibiotic-resistance markers on host cells. Insertional inactivation of the various antibiotic-resistance markers occurred at the BclI site of pE12, and the Sau96- or AvaII-site of pMK148; only a slight inactivation of the chloramphenicol-resistance marker occurred at the HaeIII-site of pC194. The chimeric plasmids pCT20 and pCE10 are both stable in S. aureus and S. carnosus. In addition, the hybrid plasmids of pCT20 and pCE10, containing lambda-DNA fragments in various restriction sites between 0.4 and 1.2 kb, are stably maintained. The inserted lambda-DNA fragments appear unchanged.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0147-619X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
270-8
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:6318248-Chloramphenicol,
pubmed-meshheading:6318248-Chromosome Mapping,
pubmed-meshheading:6318248-Cloning, Molecular,
pubmed-meshheading:6318248-DNA, Recombinant,
pubmed-meshheading:6318248-Drug Resistance, Microbial,
pubmed-meshheading:6318248-Erythromycin,
pubmed-meshheading:6318248-Genetic Vectors,
pubmed-meshheading:6318248-Plasmids,
pubmed-meshheading:6318248-Staphylococcus,
pubmed-meshheading:6318248-Tetracycline
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pubmed:year |
1983
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pubmed:articleTitle |
Construction and characterization of plasmid vectors for cloning in Staphylococcus aureus and Staphylococcus carnosus.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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