DNA polymerase I: Difference between revisions

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DNA polymerase I is an enzyme that is involved in DNA replication in [[E.Coli|''E''''.coli''''']]
DNA polymerase I is an enzyme that is involved in [[DNA|DNA]] replication in ''[[Escherichia coli|Escherichia coli]]''. It is part of a group of [[DNA polymerase|DNA polymerases]] that copy [[DNA|DNA]]; they are highly coordinated in order to replicate whole genomes precisely and rapidly. DNA polymerase I is a slow, non-processive [[Enzyme|enzyme]] that fills the gaps between [[Okazaki fragment|Okazaki]] fragments of the lagging strand by Watson-Crick base pairing. The [[Enzyme|enzyme]] has two additional activites:


1) 5’→3’ exonuclease activity to remove RNA primers ahead of the polymerase site<ref>Berg J, Tymoczko J, Stryer L (2007) Biochemistry, 6th edition, New York: W.H. Freeman, p. 801</ref>.<br>2) 3’→5’ exonuclease activity for proof-reading and accuracy.  
#5’→3’ [[Exonuclease|exonuclease]] activity to remove RNA primers ahead of the polymerase site&nbsp;<ref>Berg J, Tymoczko J, Stryer L (2007) Biochemistry, 6th edition, New York: W.H. Freeman, p. 801</ref>.
#3’→5’ [[Exonuclease|exonuclease]] activity for proof-reading and accuracy.


=== References  ===
=== References  ===


<references />
<references />

Latest revision as of 22:45, 27 November 2010

DNA polymerase I is an enzyme that is involved in DNA replication in Escherichia coli. It is part of a group of DNA polymerases that copy DNA; they are highly coordinated in order to replicate whole genomes precisely and rapidly. DNA polymerase I is a slow, non-processive enzyme that fills the gaps between Okazaki fragments of the lagging strand by Watson-Crick base pairing. The enzyme has two additional activites:

  1. 5’→3’ exonuclease activity to remove RNA primers ahead of the polymerase site [1].
  2. 3’→5’ exonuclease activity for proof-reading and accuracy.

References

  1. Berg J, Tymoczko J, Stryer L (2007) Biochemistry, 6th edition, New York: W.H. Freeman, p. 801