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Direct evidence for cyanide-insensitive quinol oxidase (alternative oxidase) in apicomplexan parasite Cryptosporidium parvum: phylogenetic and therapeutic implications
- Source :
- Biochemical and Biophysical Research Communications. 313:1044-1052
- Publication Year :
- 2004
- Publisher :
- Elsevier BV, 2004.
-
Abstract
- Cryptosporidium parvum is a parasitic protozoan that causes the diarrheal disease cryptosporidiosis, for which no satisfactory chemotherapy is currently available. Although the presence of mitochondria in this parasite has been suggested, its respiratory system is poorly understood due to difficulties in performing biochemical analyses. In order to better understand the respiratory chain of C. parvum, we surveyed its genomic DNA database in GenBank and identified a partial sequence encoding cyanide-insensitive alternative oxidase (AOX). Based on this sequence, we cloned C. parvum AOX (CpAOX) cDNA from the phylum apicomplexa for the first time. The deduced amino acid sequence (335 a.a.) of CpAOX contains diiron coordination motifs (-E-, -EXXH-) that are conserved among AOXs. Phylogenetic analysis suggested that CpAOX is a mitochondrial-type AOX, possibly derived from mitochondrial endosymbiont gene transfer. The recombinant enzyme expressed in Escherichia coli showed quinol oxidase activity. This activity was insensitive to cyanide and highly sensitive to ascofuranone, a specific inhibitor of trypanosome AOX.
- Subjects :
- Alternative oxidase
Molecular Sequence Data
Biophysics
Respiratory chain
Cryptosporidiosis
Biology
Biochemistry
Microbiology
chemistry.chemical_compound
Phylogenetics
Complementary DNA
parasitic diseases
Animals
Humans
Amino Acid Sequence
Cloning, Molecular
Enzyme Inhibitors
Molecular Biology
Peptide sequence
Phylogeny
Cryptosporidium parvum
Base Sequence
Sequence Homology, Amino Acid
Cell Biology
DNA, Protozoan
biology.organism_classification
Recombinant Proteins
Mitochondria
Ascofuranone
chemistry
GenBank
Oxidoreductases
Sesquiterpenes
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 313
- Database :
- OpenAIRE
- Journal :
- Biochemical and Biophysical Research Communications
- Accession number :
- edsair.doi.dedup.....532db08e9a965a7b4ed6d087b98f8d8e
- Full Text :
- https://doi.org/10.1016/j.bbrc.2003.12.038