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Cloning, expression, and characterization of iron-containing superoxide dismutase from Neospora caninum.

Authors
Cho, MH; Na, BK; Song, KJ; Cho, JH; Kang, SW; Lee, KH; Song, CY; Kim, TS
Citation
The Journal of parasitology, 90(2):278-285, 2004
Journal Title
The Journal of parasitology
ISSN
0022-33951937-2345
Abstract
A gene encoding superoxide dismutase (SOD) from Neospora caninum, a causative agent of neosporosis, has been cloned and its gene product functionally expressed and characterized. The gene had an open reading frame of 606 bp and deduced 201 amino acids. Sequence analysis showed that the gene had conserved metal-binding residues and conserved amino acid residues that were found in Fe-SODs. Comparison of the deduced amino acid sequence of the enzyme with previously reported Fe-SOD amino acid sequences of the other parasitic protozoans revealed significant high homology. The coding region of the N. caninum Fe-SOD was cloned and functionally expressed in Escherichia coli. Enzyme activity of the expressed protein was inhibited by hydrogen peroxide but not by sodium azide and potassium cyanide, and the enzyme showed similar biochemical properties with typical Fe-SODs of other parasitic protozoans. Southern blot analysis showed that the SOD gene appears to be present as a single-copy gene in N. caninum genome. Semiquantitative reverse transcription-polymerase chain reaction and immunoblot using antiserum raised against the purified recombinant protein showed that Fe-SOD is expressed in both developmental stages of N. caninum, i.e., in bradyzoites and tachyzoites. In an immunofluorescence assay, the enzyme was localized on the cell surface of N. caninum tachyzoites. These results suggest that Fe-SOD might be essential for the intracellular survival of N. caninum and may play an important role in the pathogenesis of the parasite by protecting the parasite from oxidative killing.
MeSH terms
Amino Acid SequenceAnimalsBlotting, NorthernBlotting, SouthernCloning, MolecularDNA, Complementary/biosynthesis/chemistryElectrophoresis, Polyacrylamide GelFluorescent Antibody Technique, IndirectGene Expression Regulation, EnzymologicHydrogen-Ion ConcentrationMolecular Sequence DataNeospora/*enzymology/geneticsPolymerase Chain ReactionRNA, Messenger/genetics/isolation & purificationSequence AlignmentSequence Homology, Amino AcidSuperoxide Dismutase/chemistry/*genetics/metabolism
DOI
10.1645/GE-3222
PMID
15165050
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Microbiology
AJOU Authors
송, 경주
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