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PMID: 6104665 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

A prepriming DNA replication enzyme of Escherichia coli. I. Purification of protein n': a sequence-specific, DNA-dependent ATPase.

The Journal of biological chemistry ·Vol. 255 ·No. 14 ·1980-07-25 ·Pages 6789-93

Shlomai J, Kornberg A

Abstract

Protein n', an enzyme essential for in vitro conversion of single-stranded phiX174 DNA to the duplex replicative form, has been purified about 16,000-fold from Escherichia coli. The enzyme is a single polypeptide chain with a native molecular weight of 76,000; about 70 enzyme molecules are present in an E. coli cell. Nearly homogeneous preparations display an ATPase (dATPase) activity which depends on a unique sequence in the phiX174 DNA. Replicative activity of n' protein and its phiX174 DNA-dependent ATPase activity were present in a constant ratio during the latter stages of purification, upon sedimentation in a glycerol gradient, and during heat inactivation. Further studies of the properties of protein n' are presented in a succeeding paper.

MeSH Terms
Adenosine Triphosphatases/isolation & purification,metabolism Bacteriophage phi X 174 Base Sequence DNA Helicases/isolation & purification,metabolism DNA Replication DNA, Viral Escherichia coli/enzymology Kinetics Molecular Weight Substrate Specificity
Chemicals
DNA, Viral Adenosine Triphosphatases DNA Helicases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Shlomai J
Kornberg A
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1980-07-25
Pages
6789-93
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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