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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1973 May;70(5):1613–1618. doi: 10.1073/pnas.70.5.1613

Studies on In Vitro DNA Synthesis Purification of the dna G Gene Product from Escherichia coli*

Sue Wickner 1, Michel Wright 1, Jerard Hurwitz 1
PMCID: PMC433553  PMID: 4197093

Abstract

ϕX174 DNA-dependent dNMP incorporation is temperature-sensitive (ts) in extracts of uninfected E. coli dna A, B, C, D, E, and G ts strains. DNA synthesis can be restored in heat-inactivated extracts of various dna ts mutants by addition of extracts of wild-type or other dna ts mutants. A protein that restores activity to heat-inactivated extracts of dna G ts cells has been extensively purified. This protein has also been purified from dna G ts cells and is thermolabile when compared to the wild-type protein. The purified dna G protein has a molecular weight of about 60,000, is insensitive to N-ethylmaleimide, and binds poorly to DNA. It does not stimulate heat-inactivated crude extracts of dna B, C, D, or E ts cells and lacks detectable RNA and DNA polymerase activities.

Keywords: dna A, dna B, dna C, dna D, and dna E gene products; ϕX174; DNA replication; DNA polymerase III

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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