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Peculiarities of recognition of CC A / T GG sequences in DNA by restriction endonucleases Mva I and Eco RII
Author(s) -
Gromova Elizabeth S.,
Kubareva Elena A.,
Vinogradova Mari.,
Oretskaya Tatjana S.,
Shabarova Zoe A.
Publication year - 1991
Publication title -
journal of molecular recognition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.401
H-Index - 79
eISSN - 1099-1352
pISSN - 0952-3499
DOI - 10.1002/jmr.300040405
Subject(s) - endonuclease , cleave , restriction enzyme , dna , chemistry , nucleotide , hydrolysis , stereochemistry , substrate (aquarium) , base pair , enzyme , phosphate , biochemistry , biology , gene , ecology
Abstract To elucidate the mechanism of action of restriction endonucleases Mva I and Eco RII a study was made of their interaction with a set of synthetic substrates in which the heterocyclic bases or the sugar–phosphate backbone had been modified; individual nucleotide residues had been removed or replaced with hydrocarbon bridges, and mismatched base pairs had been introduced. The groups of atoms in the heterocyclic bases and the phosphates in the recognition site that produce the most significant influence on the functioning of endonucleases Mva I and Eco RII were discerned. Profound differences were found in the functioning of the Mva I and Eco RII neo‐schizomers. The catalytic activity of Eco RII is significantly affected by any alteration in the recognition site structure and conformation, with a modification in one strand of the substrate causing the same decrease in the hydrolysis rate of both strands. Endonuclease Mva I is tolerant to a number of structural abnormalities; the latter sometimes affect only hydrolysis of one strand of the recognition site. The enzyme can preferentially cleave one of the substrate strands. Mismatched base pairs retard and sometimes block the hydrolysis. The effect depends on the particular enzyme, mismatch and its location.