FEBS Letters · 1996 · 13 citations · 30 references
Life SciencesBiochemistryMolecular BiologyEnzyme MechanismEnzymologyNucleic Acid BiochemistryCatalytic MechanismsEnzyme FunctionEnzyme SpecificityEnzyme-substrate RecognitionNucleic Acid CleavageSubstrate SpecificityCatalytic ActivityCatalytic Dna CleavageCatalytic Reaction MechanismsDna CleavageDna Cleavage MechanismRestriction Endonuclease SpecificityRestriction EndonucleasesRestriction Enzyme Digestion
The amino acid Asp-59 was proposed to be involved in EcoRI catalyzed DNA cleavage (Cheng et al., EMBO J. 13, 3927-35, 1994). We have tested this hypothesis by site directed mutagenesis experiments. The four mutants D59A, D59E, D59G, and D59N bind with similar stability to the specific recognition sequence as wild type EcoRI. The D59E mutant cleaves DNA as fast as the wild type enzyme. Specific activities of the other three mutants are five to tenfold lower. Therefore, we conclude that Asp-59 is not involved in catalysis of the EcoRI restriction endonuclease. Consequences for catalytic mechanisms of EcoRI and other restriction enzymes are discussed.
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Refinement of Eco RI Endonuclease Crystal Structure: A Revised Protein Chain Tracing
Youngchang Kim, John Grable, Robert A. Love et al. · Science · 1990 · 338 citations