Characterization of anEcoR 124I restriction-modification enzyme produced from a deleted form of the DNA-binding subunit, which results in a novel DNA specificity
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Microbiology
Link
http://link.springer.com/content/pdf/10.1007/BF02931361.pdf
Reference21 articles.
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2. Abadjieva A., Patel J., Zinkevich V., Firman K.: Deletions within the DNA recognition subunit of M.EcoR124I that identify a region involved in protein-protein interactions between HsdS and HsdM.J.Mol.Biol. 241, 35–43 (1994).
3. Barcus V.A., Titheradge A.J.B., Murray N.E.: The diversity of alleles at thehsd locus in natural populations ofEscherichia coli.Genetics 140, 1187–1197 (1995).
4. Burckhardt J., Weisemann J., Yuan R.: Characterization of the DNA methylase activity of the restriction enzyme fromEscherichia coli K.J.Biol.Chem. 256, 4024–4032 (1981).
5. Cowan G.M., Daniel A.S., Gann A.A.F., Kelleher J.E., Murray N.E.: Defining domains in type-I restriction and modification enzymes.Gene 74, 239–241 (1988).
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1. EcoR124I: from Plasmid-Encoded Restriction-Modification System to Nanodevice;Microbiology and Molecular Biology Reviews;2008-06
2. Characterization of a complex restriction-modification system detected inStaphylococcus aureus andStreptococcus agalactiae strains isolated from infections of domestic animals;Folia Microbiologica;2004-05
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