• Refine Query
  • Source
  • Publication year
  • to
  • Language
  • 3
  • Tagged with
  • 4
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Biochemical and structural analysis of the p58C and p68N domains of DNA polymerase alpha/primase

Weiner, Brian Edward. January 2008 (has links)
Thesis (Ph. D. in Biochemistry)--Vanderbilt University, Aug. 2008. / Title from title screen. Includes bibliographical references.
2

Kinetics of DNA polymerase conformational changes during nucleotide binding and incorporation

Tsai, Yu-chih, Johnson, Kenneth A., January 2005 (has links) (PDF)
Thesis (Ph. D.)--University of Texas at Austin, 2005. / Supervisor: Kenneth A. Johnson. Vita. Includes bibliographical references.
3

Isolation and characterisation of a novel archaeal DNA polymerase

Cooper, Christopher D. O. January 2012 (has links)
DNA replication is a key process required by organisms during cell division, with a concomitant requirement for genome synthesis by DNA polymerases. Biotechnological exploitation of thermostable DNA polymerases for DNA amplification by the Polymerase Chain Reaction (PCR), provides a significant market for novel enzymes or those with improved properties. An approach was taken to isolate alternative thermostable DNA polymerases, by enriching thermophilic bacteria from a novel thermal environment, aerobically spoiling silage. In addition, a novel DNA polymerase (Abr polBl) was cloned from the thermoacidophilic archaeon, Acidianus brierleyi, with the intention of characterising its in vivo role and application to PCR. Protein sequence analysis suggested a proofreading (high fidelity) DNA synthesis activity most related to polBl DNA polymerases from Crenarchaeota. Abr polBl was heterologously expressed in bacteria and protein purified to homogeneity. Biochemical assays confirmed high-temperature DNA polymerase and 3'-5'exonuclease activities of Abr polBl, with an accompanying proofreading ability. Sequence analysis, processivity, strand displacement and lesion bypass activities indicated potential roles in genome replication and DNA repair. Abr polBl could not amplify DNA under a range of PCR conditions, presumably following its low intrinsic thermostability. Biophysical analyses confirmed irreversible unfolding of Abr polBl at temperatures required for PCR. Supplementation with organic compounds and ionic salts stabilised Abr polBl, promoting retention of conformational stability and DNA synthesis activity following thermal incubation, but could not promote DNA amplification with Abr polB 1.
4

The role of human Rev7, the accessory subunit of human DNA polymerase zeta, in cell survival and DNA damage induced mutagenesis

Neal, Jessica A. January 2008 (has links)
Thesis (PH. D.)--Michigan State University. Biochemistry and Molecular Biology, 2008. / Title from PDF t.p. (viewed on Sept. 2, 2009) Includes bibliographical references. Also issued in print.

Page generated in 0.1021 seconds