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PMID: 2821901 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

In vivo formation of gene fusions in Pseudomonas putida and construction of versatile broad-host-range vectors for direct subcloning of Mu d1 and Mu d2 fusions.

Applied and environmental microbiology ·Vol. 53 ·No. 7 ·1987-07-00 ·Pages 1649-54

Simon V, Schumann W

Abstract

The Mu d1 and Mu d2 prophages were integrated into the conjugative broad-host-range plasmid R751. The two plasmids were then transferred into Pseudomonas putida, and derivatives carrying intact Mu prophages were recovered. After induction of Mu at 42 degrees C, both operon and gene fusions were observed on 5-bromo-4-chloro-3-indolyl-beta-D-galactopyranoside (X-Gal) plates. Broad-host-range vectors were constructed which allow direct cloning of both operon or gene fusions and their analysis in Escherichia coli and P. putida. By using one of these vectors, two operon fusions were isolated from the P. putida chromosome and comparatively analyzed in E. coli and P. putida.

MeSH Terms
Bacteriophages/genetics Cloning, Molecular Conjugation, Genetic DNA Restriction Enzymes DNA Transposable Elements DNA, Bacterial/genetics Deoxyribonuclease BamHI Escherichia coli/genetics Genes, Bacterial Genetic Vectors Nucleic Acid Hybridization Operon Plasmids Protein Biosynthesis Pseudomonas/genetics Transcription, Genetic
Chemicals
DNA Transposable Elements DNA, Bacterial DNA Restriction Enzymes Deoxyribonuclease BamHI
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Simon V
Lehrstuhl für Genetik, Universität Bayreuth, Federal Republic of Germany.
Schumann W
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Article Info
Journal
Applied and environmental microbiology
Abbr.
Appl Environ Microbiol
ISSN
0099-2240
Published
1987-07-00
Pages
1649-54
Language
English
Region
United States
NLM ID
7605801
PMCID
PMC203925
Subset
IM
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