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PMID: 347245 Published · ppublish English Journal Article

Cloning of a restriction fragment of phage mu DNA coding for early functions.

Molecular & general genetics : MGG ·Vol. 160 ·No. 1 ·1978-03-20 ·Pages 115-8

Schumann W, Bade EG, Delius H, Hübert P

Abstract

The DNA of an E. coli K12 strain harboring ten wildtype Mu prophages was restricted with endonuclease EcoRI, and the fragments ligated into the plasmid vector pMB9. Upon transformation of a strain carrying a heat inducible (Mu cts62) prophage, one temperature-resistant transformant was isolated. This transformant strain harbors the hybrid plasmid pKN001, containing the EcoRI.C fragment of Mu DNA as shown by restriction and heteroduplex analysis. Stable transformants of pKN001 are immune to superinfection with phage Mu. Transformation of Mu sensitive bacteria with pKN001 results in killing of the recipients (10(-4) surviving bacteria). The killing function is not expressed upon transformation of Mu-immune (lysogenic) bacteria.

MeSH Terms
Cell Transformation, Viral Coliphages/genetics DNA, Bacterial/genetics DNA, Recombinant/genetics DNA, Viral/genetics Escherichia coli/genetics Genes, Viral Plasmids
Chemicals
DNA, Bacterial DNA, Recombinant DNA, Viral
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Schumann W
Bade E G
Delius H
Hübert P
References (9)
9 references, click to expand
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  8. Biochemical method for inserting new genetic information into DNA of Simian Virus 40: circular SV40 DNA molecules containing lambda phage genes and the galactose operon of Escherichia coli.
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Article Info
Journal
Molecular & general genetics : MGG
Abbr.
Mol Gen Genet
ISSN
0026-8925
Published
1978-03-20
Pages
115-8
Language
English
Region
Germany
NLM ID
0125036
Subset
IM
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