Trypanosomatids are parasitic eukaryotic organisms that cause human disease. These organisms have complex lifestyles; cycling between vertebrate and insect hosts and alternating between two morphologies; a replicating form and an infective, nonreplicating one. Because trypanosomatids are one of the few organisms that do not synthesize the essential cofactor, heme, these parasites sequester the most common form, heme B, from their hosts. Once acquired, the parasites derivatize heme B to heme A by two sequential enzyme reactions. Although heme C is found in many cytochrome c and c1 proteins, heme A is the cofactor of only one known protein, cytochrome c oxidase (CcO). In a recent issue of the Biochemical Journal, Merli et al. [Biochem. J. (2017) 474, 2315–2332] demonstrate that the final step in the synthesis of heme A by heme A synthase (TcCox15) and the subsequent activity of CcO are essential for infectivity and replication of Trypanosoma cruzi.
Commentary| August 31 2017
From B to A: making an essential cofactor in a human parasite
Naomi S. Morrissette;
Celia W. Goulding
1Departments of Molecular Biology and Biochemistry, University of California Irvine, Irvine, CA 92697, U.S.A.
2Pharmaceutical Sciences, University of California Irvine, Irvine, CA 92697, U.S.A.
Correspondence: Celia W. Goulding (email@example.com)
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Naomi S. Morrissette, Celia W. Goulding; From B to A: making an essential cofactor in a human parasite. Biochem J 15 September 2017; 474 (18): 3089–3092. doi: https://doi.org/10.1042/BCJ20170446
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