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PMID: 6287460 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Involvement of outside DNA sequences in the major kinetic path by which EcoRI endonuclease locates and leaves its recognition sequence.

Jack WE, Terry BJ, Modrich P

Abstract

We have examined the kinetics of the interaction between endodeoxyribonuclease EcoRI (EC 3.1.23.13) and nine linear DNA fragments that range in size between 34 and 6,200 base pairs and contain the EcoRI site of plasmid pBR322 in a central location. The kinetic parameters governing both formation and decay of specific endonuclease . DNA complexes increase 8-fold with increasing chain length over this size range. In contrast, equilibrium competition experiments demonstrated that the intrinsic affinity of endonuclease for its recognition sequence is independent of DNA chain length over this range. Thus, DNA sequences outside the recognition site enhance the rate at which EcoRI endonuclease locates or leaves its recognition site without affecting the intrinsic thermodynamic parameters of site-specific interaction. These results are consistent with a facilitated diffusion mechanism for specific DNA site location by this enzyme.

MeSH Terms
Base Sequence DNA Restriction Enzymes/metabolism Deoxyribonuclease EcoRI Kinetics Plasmids Substrate Specificity
Chemicals
DNA Restriction Enzymes Deoxyribonuclease EcoRI
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Jack W E
Terry B J
Modrich P
References (27)
27 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1982-07-00
Pages
4010-4
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC346566
Subset
IM
Grants
NCI NIH HHS · CA 00495 · United States
NIGMS NIH HHS · GM23719 · United States
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