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PMID: 372561 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Construction and characterization of the hybrid bacteriophage lambda Charon vectors for DNA cloning.

Journal of virology ·Vol. 29 ·No. 2 ·1979-02-00 ·Pages 555-75

Williams BG, Blattner FR

Abstract

Twenty hybrid lambda phages especially designed for molecular cloning have been constructed and named Charon phages. These phages differ in the ranges of sizes of DNA fragments that may be inserted, by the selections and screens which may be used to isolate and detect the incorporation of cloned fragments, by the way transcription of the cloned fragment may be controlled, by the different restriction enzymes that can be used for cloning, by the phage immunities that may be employed for controlling replication and transcription, and by the biological safety features that they contain. The crosses used to produce the vectors are described, and their genealogy is discussed. The structure of each vector has been verified by genetic tests, by DNA length determinations, by electron micrographic analysis of DNA heteroduplexes, and by gel electrophoresis of restriction enzyme digests. In the course of these constructions, a new EcoRI site was found in a derivative of lambda Aam32Bam1 which maps very near the left cohesive end of lambda.

MeSH Terms
Coliphages/genetics DNA, Bacterial/genetics DNA, Recombinant DNA, Viral/genetics Escherichia coli/genetics Hybridization, Genetic Mutation Phenotype
Chemicals
DNA, Bacterial DNA, Recombinant DNA, Viral
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Williams B G
Blattner F R
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1979-02-00
Pages
555-75
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC353190
Subset
IM
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