Publication: Molecular characterization of Plasmodium falciparum putative polynucleotide kinase/phosphatase
Issued Date
2011-11-01
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ISSN
18729428
01666851
01666851
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2-s2.0-80052699697
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Mahidol University
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SCOPUS
Bibliographic Citation
Molecular and Biochemical Parasitology. Vol.180, No.1 (2011), 1-7
Suggested Citation
Saranya Siribal, Michael Weinfeld, Feridoun Karimi-Busheri, J. N. Mark Glover, Nina K. Bernstein, Danny Aceytuno, Porntip Chavalitshewinkoon-Petmitr Molecular characterization of Plasmodium falciparum putative polynucleotide kinase/phosphatase. Molecular and Biochemical Parasitology. Vol.180, No.1 (2011), 1-7. doi:10.1016/j.molbiopara.2011.06.007 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/11443
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Title
Molecular characterization of Plasmodium falciparum putative polynucleotide kinase/phosphatase
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Abstract
Polynucleotide kinase/phosphatase (PNKP) is a bifunctional enzyme that can phosphorylate the 5′-OH termini and dephosphorylate the 3′-phosphate termini of DNA. It is a DNA repair enzyme involved in the processing of strand break termini, which permits subsequent repair proteins to replace missing nucleotides and rejoin broken strands. Little is known about DNA repair in Plasmodium falciparum, including the roles of PNKP in repairing parasite DNA. We identified a P. falciparum gene encoding a protein with 24% homology to human PNKP and thus suggestive of a putative PNKP. In this study, the PNKP gene of P. falciparum strain K1 (PfPNKP) was successfully cloned and expressed in E. coli as a GST-PfPNKP recombinant protein. MALDI-TOF/TOF analysis of the protein confirmed the identity of PfPNKP. Assays for enzymatic activity were carried out with a variety of single- and double-stranded substrates. Although 3′-phosphatase activity was detected, PfPNKP was observed to dephosphorylate single-stranded substrates or double-stranded substrates with a short 3′-single-stranded overhang, but not double-stranded substrates that mimicked single-strand breaks. We hypothesize that unlike human PNKP, PfPNKP may not be involved in single-strand break repair, since alternative terminal processing mechanisms can substitute for PfPNKP, and that PfPNKP DNA repair actions may be confined to overhanging termini of double-strand breaks. © 2011 Elsevier B.V. All rights reserved.