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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
1992-7-30
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pubmed:abstractText |
IS493 is an insertion sequence isolated from Streptomyces lividans by a method designed to 'trap' transposable elements. IS493 was converted to functional transposons by cloning antibiotic-resistance-encoding genes between ORF-A and ORF-B of IS493 or near the left-end inverted repeat of the element. Tn5096 transposed relatively randomly in several Streptomyces species. Tn5096 can be introduced into streptomycetes on temperature-sensitive vectors by protoplast transformation, FP43-mediated transduction, or by conjugation from Escherichia coli. We have shown that additional genes can be inserted in Tn5096 without disrupting transposition, and that Tn5096 insertions in a tylosin (Ty)-producing strain of Streptomyces fradiae frequently cause no deleterious effects on Ty production. A promoter probe transposon, Tn5099, containing a promoterless xylE gene, transposed in Streptomyces griseofuscus and S. fradiae, and transcriptional fusions were readily identified.
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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 |
Jun
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pubmed:issn |
0378-1119
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
115
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
61-5
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:1319378-Cloning, Molecular,
pubmed-meshheading:1319378-Conjugation, Genetic,
pubmed-meshheading:1319378-DNA Probes,
pubmed-meshheading:1319378-DNA Transposable Elements,
pubmed-meshheading:1319378-Escherichia coli,
pubmed-meshheading:1319378-Genes, Bacterial,
pubmed-meshheading:1319378-Promoter Regions, Genetic,
pubmed-meshheading:1319378-Streptomyces,
pubmed-meshheading:1319378-Transduction, Genetic,
pubmed-meshheading:1319378-Tylosin
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pubmed:year |
1992
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pubmed:articleTitle |
Transposition of Tn5096 and related transposons in Streptomyces species.
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pubmed:affiliation |
Lilly Research Laboratories, Indianapolis, IN 46285.
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pubmed:publicationType |
Journal Article
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