EcoRI (pronounced "eco R one") is a restriction endonuclease enzyme isolated from species E. coli. It is a restriction enzyme that cleaves DNA double helices into fragments at specific sites, and is also a part of the restriction modification system. The Eco part of the enzyme's name originates from the species from which it was isolated - "E" denotes generic name which is "Escherichia" and "co" denotes species name, "coli" - while the R represents the particular strain, in this case RY13, and the I denotes that it was the first enzyme isolated from this strain.
In molecular biology it is used as a restriction enzyme. EcoRI creates 4 nucleotide sticky ends with 5' end overhangs of AATT. The nucleic acid recognition sequence where the enzyme cuts is G↓AATTC, which has a palindromic, complementary sequence of CTTAA↓G. Other restriction enzymes, depending on their cut sites, can also leave 3' overhangs or blunt ends with no overhangs.
EcoRI is an example of type II restriction enzymes which now has more the 300 enzymes with more than 200 different sequence-specificities, which has transformed molecular biology and medicine.
EcoRI was isolated by PhD student Robert Yoshimori who investigated clinical E. coli isolates which contained restriction systems presented on its plasmids. The purified isolates became known as EcoRI that is used to cleave G’AATTC.
EcoRI contains the PD..D/EXK motif within its active site like many restriction endonucleases.
The enzyme is a homodimer of a 31 kilodalton subunit consisting of one globular domain of the α/β architecture. Each subunit contains a loop which sticks out from the globular domain and wraps around the DNA when bound.
EcoRI has been cocrystallized with the sequence it normally cuts. This crystal was used to solve the structure of the complex (). The solved crystal structure shows that the subunits of the enzyme homodimer interact with the DNA symmetrically. In the complex, two α-helices from each subunit come together to form a four-helix bundle.
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thumb|L'enzyme de restriction EcoRV (en vert) avec son substrat : l'ADN. Une enzyme de restriction est une protéine capable de couper un fragment d'ADN au niveau d'une séquence de nucléotides caractéristique appelée site de restriction. Chaque enzyme de restriction reconnaît ainsi un site spécifique. Plusieurs centaines d'enzymes de restriction sont actuellement connues. Naturellement présentes chez un grand nombre d'espèces de bactéries, ces enzymes sont devenues des outils importants en génie génétique.
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