The goal of the proposed project is to test the hypothesis that core metabolism of the medically important cavity parasites of humans, the amitochondriate Giardia lamblia, Entamoeba histolytica and Trichomonas vaginalis differs markedly from that of their human host. It will also be explored to what extent the unique and diverse """"""""chimeric"""""""" metabolic patterns of these organisms are due to evolutionary losses or new acquisitions of enzymes. In the next grant period emphasis will be placed on two critical but essentially unexplored aspects of """"""""amitochondriate"""""""" parasites, a) carbohydrate (glycogen) reserves and their regulation and, b) enzymes involved in electron transport, to complement accumulating data on glycolysis and its distal extensions. a) Enzymes involved in the mobilization of glucose from glycogen and of glycogen synthesis will be expressed in heterologous systems, purified and studied with biochemical methods, with special emphasis on their regulatory properties. In addition, both the sequences and physiological characteristics of the enzymes will be evaluated in comparison with existing data in order to obtain insight into their evolutionary relationships. b ) Enzymes transferring reducing equivalents from glycolytically reduced NADH and ferredoxin to diverse electron acceptors and O2 will be explored with essentially the same approaches.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI011942-26
Application #
6372955
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Program Officer
Rogers, Martin J
Project Start
1978-07-01
Project End
2004-05-31
Budget Start
2001-06-01
Budget End
2002-05-31
Support Year
26
Fiscal Year
2001
Total Cost
$334,000
Indirect Cost
Name
Rockefeller University
Department
Microbiology/Immun/Virology
Type
Other Domestic Higher Education
DUNS #
071037113
City
New York
State
NY
Country
United States
Zip Code
10065
Müller, Miklós; Mentel, Marek; van Hellemond, Jaap J et al. (2012) Biochemistry and evolution of anaerobic energy metabolism in eukaryotes. Microbiol Mol Biol Rev 76:444-95
Sutak, Robert; Hrdy, Ivan; Dolezal, Pavel et al. (2012) Secondary alcohol dehydrogenase catalyzes the reduction of exogenous acetone to 2-propanol in Trichomonas vaginalis. FEBS J 279:2768-80
Yee, Janet; Tang, Anita; Lau, Wei-Ling et al. (2007) Core histone genes of Giardia intestinalis: genomic organization, promoter structure, and expression. BMC Mol Biol 8:26
Arisue, Nobuko; Hasegawa, Masami; Hashimoto, Tetsuo (2005) Root of the Eukaryota tree as inferred from combined maximum likelihood analyses of multiple molecular sequence data. Mol Biol Evol 22:409-20
Arisue, Nobuko; Maki, Yasushi; Yoshida, Hideji et al. (2004) Comparative analysis of the ribosomal components of the hydrogenosome-containing protist, Trichomonas vaginalis. J Mol Evol 59:59-71
Sutak, Robert; Dolezal, Pavel; Fiumera, Heather L et al. (2004) Mitochondrial-type assembly of FeS centers in the hydrogenosomes of the amitochondriate eukaryote Trichomonas vaginalis. Proc Natl Acad Sci U S A 101:10368-73
Chow, Billy K C; Moon, Thomas W; Hoo, Ruby L C et al. (2004) Identification and characterization of a glucagon receptor from the goldfish Carassius auratus: implications for the evolution of the ligand specificity of glucagon receptors in vertebrates. Endocrinology 145:3273-88
Jordan, I King; Henze, Katrin; Fedorova, Natalie D et al. (2003) Phylogenomic analysis of the Giardia intestinalis transcarboxylase reveals multiple instances of domain fusion and fission in the evolution of biotin-dependent enzymes. J Mol Microbiol Biotechnol 5:172-89
Wu, Gang; Muller, Miklos (2003) Glycogen phosphorylase sequences from the amitochondriate protists, Trichomonas vaginalis, Mastigamoeba balamuthi, Entamoeba histolytica and Giardia intestinalis. J Eukaryot Microbiol 50:366-72
Vernal, Javier; Fiser, Andras; Sali, Andrej et al. (2002) Probing the specificity of a trypanosomal aromatic alpha-hydroxy acid dehydrogenase by site-directed mutagenesis. Biochem Biophys Res Commun 293:633-9

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