Identification of a Functional Type IA Topoisomerase,LdTopIIIβ, from Kinetoplastid ParasiteLeishmania donovani
Author(s) -
Bijoylaxmi Banerjee,
Nilkantha Sen,
Hemanta K. Majumder
Publication year - 2011
Publication title -
enzyme research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.439
H-Index - 39
eISSN - 2090-0406
pISSN - 2090-0414
DOI - 10.4061/2011/230542
Subject(s) - kinetoplast , topoisomerase , biology , mutant , complementation , leishmania donovani , dna , saccharomyces cerevisiae , microbiology and biotechnology , genetics , biochemistry , gene , leishmaniasis , visceral leishmaniasis
DNA topoisomerases of kinetoplastids represent a family of DNA processing enzymes that essentially solve the topological problems not only in nuclear DNA but also in kinetoplast DNA. We have, for the first time, identified a Leishmania donovani homologue of bacterial and eukaryotic IA type of topoisomerase III protein and termed as LdTopIIIβ. Complementation study of wild-type and mutant LdTopIIIβ with slow-growing topoisomerase III mutant yeast S. cerevisiae revealed the functional conservation of the leishmanial counterpart of topoisomerase IIIβ protein, the 327 tyrosine being the active site amino acid. A C-terminal deletion construct of LdTopIIIβ could not suppress the slow-growth phenotype of mutant yeast, indicating the requirement of C-terminal region for the enzyme function in vivo.LdTopIIIβ localized inside the nucleus and kinetoplast of the parasite. Taken together, our study indicates functional conservation and possible role of LdTopIIIβ in parasite DNA processing
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