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Bacteriophage lambda-E. coli K12 vector-host system for gene cloning and expression under lactose promoter control. II. DNA fragment insertion at the vicinity of the lac UV5 promoter.
Authors:Margaret L Palmer  Mary Alice Raker  Poindexter J Kennedy  Jon W Young  Wayne M Barnes  Raymond L Rodriguez and Harry F Noller
Institution:(1) Thimann Laboratories, University of California at Santa Cruz, 95064 Santa Cruz, CA, USA;(2) Present address: Dept. of Genetics, Univ. of California at Davis, 95616 Davis, CA, USA;(3) Present address: Basel Institute for Immunology, Grenzacher-strasse 487, Basel, Switzerland;(4) Present address: Dept. of Biol. Chem, Washington Univ. School of Medicine, 63110 St. Louis, Missouri, USA
Abstract:Summary Recombinant plasmids containing the entire 16S RNA gene from the rrn B cistron of E. coli inserted in Col E1 and pBR322 plasmid vectors have been constructed. These plasmids have been mapped using several restriction endonucleases as well as by DNA-RNA hybridization. These maps reveal previously undetected restriction sites in the rrn B cistron and in Col E1 plasmid DNA.
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