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    Mol Biochem Parasitol. 2006 Jul;148(1):93-8. Epub 2006 Mar 30.

    Cloning and preliminary characterization of the dihydroorotase from Toxoplasma gondii.

    Robles Lopez SM, Hortua Triana MA, Zimmermann BH.

    Department of Biochemistry, University of Puerto Rico School of Medicine, Medical Sciences Campus, San Juan, USA.

    A full-length dihydroorotase (DHOase) sequence was cloned from a Toxoplasma gondii tachyzoite cDNA library. The sequence had a calculated molecular mass of 44.2 kDa and a pI of 5.72, and was most similar to type IIa DHOases. A recombinant protein was expressed and purified with a yield of approximately 20 mg L(-1) of cell culture. Polyclonal antibodies raised against purified recombinant protein reacted with a band of the expected molecular mass in tachyzoite extracts. Specific activities of 18.3 micromol/min/mg in the biosynthetic direction and 18.4 micromol/min/mg in the degradative direction, with K(m, carbamyl aspartate) = 323 microM and K(m, dihydroorotate) = 64.3 microM, were measured for purified recombinant protein. Size exclusion chromatography/laser light scattering showed a single, monodisperse peak with a molecular mass of 45.6 kDa, suggesting that the native protein is a monomer.

    PMID: 16621066 [PubMed - indexed for MEDLINE]

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