By Katsuhiko S. Murakami, Michael A. Trakselis

ISBN-10: 3642397956

ISBN-13: 9783642397950

ISBN-10: 3642397964

ISBN-13: 9783642397967

This ebook presents a assessment of the multitude of nucleic acid polymerases, together with DNA and RNA polymerases from Archea, micro organism and Eukaryota, mitochondrial and viral polymerases, and different really good polymerases reminiscent of telomerase, template-independent terminal nucleotidyl transferase and RNA self-replication ribozyme. even though many books disguise numerous kinds of polymerases, no publication to date has tried to catalog all nucleic acid polymerases. The aim of this e-book is to be the pinnacle reference paintings for postgraduate scholars, postdocs, and precept investigators who learn polymerases of all kinds. In different phrases, this booklet is for polymerase enthusiasts via polymerase fans.

Nucleic acid polymerases play a basic position in genome replication, upkeep, gene expression and rules. all through evolution those enzymes were pivotal in reworking existence in the direction of RNA self-replicating structures in addition to into extra reliable DNA genomes. those enzymes are usually tremendous effective and exact in RNA transcription and DNA replication and proportion universal kinetic and structural positive aspects. How catalysis could be so amazingly speedy with no lack of specificity is a query that has intrigued researchers for over 60 years. definite really good polymerases that play a severe position in mobile metabolism are used for various biotechnological purposes and are consequently a necessary device for research.

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Extra info for Nucleic Acid Polymerases

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2012; Podust et al. 2002). The Pol δ p125/p50 heterodimer (also referred to as the core dimer) is a tightly associated complex with low specific activity. The three subunit complex, Pol δ3 (core + p68 subunit), displays high DNA synthesis activity but is unstable in vitro. The p68 subunit is essential for synthesis of long DNA products by Pol δ. The p12 subunit increases stability of the holoenzyme and increases DNA synthesis activity. All four subunits of human Pol δ individually interact with PCNA, which may allow for flexibility during DNA replication, as many proteins functionally interact with PCNA during Okazaki fragment maturation (Zhang et al.

Thus, phosphorylation may serve to regulate Pol δ activity by controlling its interaction with DNA and/or auxiliary proteins during replication. 1 Overview Purified Pol ε was first characterized as a larger form of Pol δ that was highly processive, but not stimulated by PCNA in vitro (Syvaoja and Linn 1989). 1) (Pursell et al. 2008). 50 exonuclease active sites within the N-terminus, and binding domains for smaller 26 E. A. Eckert subunits and PCNA within the C-terminus. The C and D subunits form a subcomplex that is important for double-stranded DNA binding (Tsubota ˚ resolution et al.

Biochemistry 49 (34):7344–7350. 1021/bi100556m Dua R, Levy DL, Campbell JL (1998) Role of the putative zinc finger domain of Saccharomyces cerevisiae DNA polymerase epsilon in DNA replication and the S/M checkpoint pathway. J Biol Chem 273(45):30046–30055. 30046 Dua R, Levy DL, Campbell JL (1999) Analysis of the essential functions of the C-terminal protein/ protein interaction domain of Saccharomyces cerevisiae pol epsilon and its unexpected ability to support growth in the absence of the DNA polymerase domain.

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Nucleic Acid Polymerases by Katsuhiko S. Murakami, Michael A. Trakselis


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