The Essential Carboxyl Group in Restriction Endonuclease EcoRI
- 1 November 1981
- journal article
- Published by Wiley in European Journal of Biochemistry
- Vol. 120 (1) , 125-128
- https://doi.org/10.1111/j.1432-1033.1981.tb05678.x
Abstract
We have carried out studies on type II restriction endonuclease EcoRI, which cleaves the DNA sequence 5'd(-G-A-A-T-T-C-)3', as indicated. The active form of the enzyme consists of two subunits, each 31063 molecular weight. A water-soluble reagent, 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide metho-p-sulphonate, which reacts with carboxyl groups and also with tyrosine and cysteine residues, has been found to inactivate this enzyme. Results are presented which show the following. (1) This specific inactivation is not due to modification of tyrosine or cysteine residues. (2) There is one carboxyl group per subunit which, when modified with carbodiimide, inactivates the enzyme. (3) phi X174 DNA (which does not contain EcoRI sites) partially protects the enzyme from the carbodiimide; protection is unaffected by the additional presence of Mg2+, but significantly greater with Co2+ and phi X174 DNA.Keywords
This publication has 17 references indexed in Scilit:
- Cation Dependence of Restriction Endonuclease EcoRI ActivityEuropean Journal of Biochemistry, 1981
- Non-specific binding of restriction endonudease EcoR1 to DNANucleic Acids Research, 1980
- Substrate activity of (adenosine triphosphato)tetraamminecobalt(III) with yeast hexokinase and separation of diastereomers using the enzymeBiochemistry, 1978
- Preliminary X-ray diffraction analysis of crystalline EcoRI endonucleaseJournal of Molecular Biology, 1978
- Specific recognition of guanine bases in protein—nucleic acid complexesFEBS Letters, 1977
- [1] Measurement of molecular weights by electrophoresis on SDS-acrylamide gelPublished by Elsevier ,1972
- Investigation of nucleic acid secondary structure by means of chemical modification with a carbodiimide reagent. I. Reaction between N-cyclohexyl-N'-β-(4-methylmorpholinium)ethylcarbodiimide and model nucleotidesBiochemistry, 1969
- Role of a Buried Acid Group in the Mechanism of Action of ChymotrypsinNature, 1969
- Reaction of tyrosine residues in proteins with carbodiimide reagentsBiochimica et Biophysica Acta (BBA) - Protein Structure, 1968
- The Chemistry of Carbodiimides.Chemical Reviews, 1953