Bacteriophage lambda-E. coli K12 vector-host system for gene cloning and expression under lactose promoter control
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology
Link
http://link.springer.com/content/pdf/10.1007/BF00337793.pdf
Reference28 articles.
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2. Arditti, R.R., Scaife, J.G., Beckwith, J.R.: The nature of mutants in the lac promoter region, J. Mol. Biol. 38, 421–426 (1968)
3. Bachmann, B.J., Pedigrees of some mutant strains of Escherichia coli K12: Bacteriol. Rev. 36, 525 (1972)
4. Backman, K., Ptashne, M., Gilbert, W., Construction: of plasmids carrying the cI gene of bacteriophage λ, Proc. Natl. Acad. Sci. U.S.A. 73, 4174–4178 (1976)
5. Beckwith, J.R.: Restoration of operon activity by suppressors, Biochim. Biophys. Acta 76, 162–164 (1963)
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2. Genetic approach to the role of tryptophan residues in the activities and fluorescence of a bacterial periplasmic maltose-binding protein;Journal of Molecular Biology;1990-07
3. Dependence on pH of substrate binding to a mutant lactose carrier, lacYun, in Escherichia coli. A model for H+/lactose symport;Biochemical Journal;1989-03-01
4. Bacteriophage Lambda Cloning Vectors;Vectors;1988
5. Silent and functional changes in the periplasmic maltose-binding protein of Escherichia coli K12;Journal of Molecular Biology;1987-04
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