Analysis of IS21-mediated mobilization of plasmid pACYC184 by R68.45 in Escherichia coli

Riess, G.; Masepohl, B.; Pühler, Alfred

Analysis of IS21-mediated mobilization of plasmid pACYC184 by R68.45 in Escherichia coli

Riess G, Masepohl B, Pühler A (1983)
Plasmid 10(2): 111-118.

Zeitschriftenaufsatz | Veröffentlicht | Englisch

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DOI

https://doi.org/10.1016/0147-619X(83)90063-X

Autor*in

Riess, G.; Masepohl, B.; Pühler, Alfred^UniBi

Einrichtung

Fakultät für Biologie

Erscheinungsjahr

1983

Zeitschriftentitel

Plasmid

Band

10

Ausgabe

2

Seite(n)

111-118

ISSN

0147-619X

Page URI

https://pub.uni-bielefeld.de/record/1659603

Zitieren

Riess G, Masepohl B, Pühler A. Analysis of IS21-mediated mobilization of plasmid pACYC184 by R68.45 in Escherichia coli. Plasmid. 1983;10(2):111-118.

Riess, G., Masepohl, B., & Pühler, A. (1983). Analysis of IS21-mediated mobilization of plasmid pACYC184 by R68.45 in Escherichia coli. Plasmid, 10(2), 111-118. https://doi.org/10.1016/0147-619X(83)90063-X

Riess, G., Masepohl, B., and Pühler, Alfred. 1983. “Analysis of IS21-mediated mobilization of plasmid pACYC184 by R68.45 in Escherichia coli”. Plasmid 10 (2): 111-118.

Riess, G., Masepohl, B., and Pühler, A. (1983). Analysis of IS21-mediated mobilization of plasmid pACYC184 by R68.45 in Escherichia coli. Plasmid 10, 111-118.

Riess, G., Masepohl, B., & Pühler, A., 1983. Analysis of IS21-mediated mobilization of plasmid pACYC184 by R68.45 in Escherichia coli. Plasmid, 10(2), p 111-118.

G. Riess, B. Masepohl, and A. Pühler, “Analysis of IS21-mediated mobilization of plasmid pACYC184 by R68.45 in Escherichia coli”, Plasmid, vol. 10, 1983, pp. 111-118.

Riess, G., Masepohl, B., Pühler, A.: Analysis of IS21-mediated mobilization of plasmid pACYC184 by R68.45 in Escherichia coli. Plasmid. 10, 111-118 (1983).

Riess, G., Masepohl, B., and Pühler, Alfred. “Analysis of IS21-mediated mobilization of plasmid pACYC184 by R68.45 in Escherichia coli”. Plasmid 10.2 (1983): 111-118.

13 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Four different integrative recombination events involved in the mobilization of the gonococcal 5.2 kb beta-lactamase plasmid pSJ5.2 in Escherichia coli.
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Cointegrase, a naturally occurring, truncated form of IS21 transposase, catalyzes replicon fusion rather than simple insertion of IS21.
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Use of a xylE marker gene to monitor survival of recombinant Pseudomonas putida populations in lake water by culture on nonselective media.
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The istA gene of insertion sequence IS21 is essential for cleavage at the inner 3' ends of tandemly repeated IS21 elements in vitro.
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Interactions between the transposable element IS21 on R68.45 and TN7 in Pseudomonas aeruginosa PAO.
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Mode of replicon fusion mediated by the duplicated insertion sequence IS21 in Escherichia coli.
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Novel rearrangements of IS30 carrying plasmids leading to the reactivation of gene expression.
Dalrymple B., Mol Gen Genet 207(2-3), 1987
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Behavior of the IncW plasmid Sa in Zymomonas mobilis.
Strzelecki AT, Goodman AE, Rogers PL., Plasmid 18(1), 1987
PMID: 2962214

IS21 insertion in the trfA replication control gene of chromosomally integrated plasmid RP1: a property of stable Pseudomonas aeruginosa Hfr strains.
Reimmann C, Haas D., Mol Gen Genet 203(3), 1986
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Vector insertion mutagenesis of Rhizobium sp. strain ORS571: direct cloning of mutagenized DNA sequences.
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pULB113, an RP4::mini-Mu plasmid, mediates chromosomal mobilization and R-prime formation in Erwinia amylovora, Erwinia chrysanthemi, and subspecies of Erwinia carotovora.
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Die Tandemduplikation der Insertions-sequenz IS21 im Plasmid R68.45 ist verantwortlich fuer die Mobilisierung des Escherichia coli Chromosoms
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