Abstract
Plasmid pSCC31 contains the EcoRI endonuclease gene downstream from lambda pL. It does not yield transformants upon introduction into Escherichia coli unless the structural integrity of the endonuclease is destroyed. This makes it useful as a positive-selection cloning vehicle which can be employed for regulated overproduction of hybrid proteins.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Reference18 articles.
1. Nucleotide sequence and genome organisation of filamentous bacteriophages fl and fd;Beck E.;Gene,1981
2. Construction and characterization of amplifiable multicopy DNA cloning vehicles derived from the P15A cryptic miniplasmid;Chang A. C. Y.;J. Bacteriol.,1978
3. A plasmid cloning vector for the direct selection of strains carrying recombinant plasmids;Dean D.;Gene,1981
4. Sequence analysis of the DNA encoding the EcoRI endonuclease and methylase;Greene P. J.;J. Biol. Chem.,1981
5. Horluchl K. G. F. Vovs and P. Model. 1978. The filamentous phage genome: genes physical structure and protein products p. 113-137. In D. T. Denhardt D. Dressler and D. S. Ray (ed.) The single-stranded DNA phages. Cold Spring Harbor Laboratory Cold Spring Harbor N.Y.
Cited by
50 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献