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Transketolase in Trypanosoma brucei

Authors :
Vincent P. Alibu
Michael P. Barrett
Jean-Charles Portais
Frédéric Bringaud
Jane Hubert
Sabine A. Stoffel
Charles Ebikeme
M. Ernst Schweingruber
Pev Biotech AG
Partenaires INRAE
University of Glasgow
Laboratoire d'Ingénierie des Systèmes Biologiques et des Procédés (LISBP)
Institut National de la Recherche Agronomique (INRA)-Institut National des Sciences Appliquées - Toulouse (INSA Toulouse)
Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Centre National de la Recherche Scientifique (CNRS)
Université de Bordeaux Ségalen [Bordeaux 2]
Universität Bern- University of Bern [Bern]
Swiss National Foundation
Wellcome Trust
Agence Nationale de la Recherche (ANR) [ANR-MIME2007]
BBSRC-ANR
Institut National des Sciences Appliquées (INSA)-Université de Toulouse (UT)-Institut National des Sciences Appliquées (INSA)-Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS)
Source :
Molecular and Biochemical Parasitology, Molecular and Biochemical Parasitology, Elsevier, 2011, 179 (1), pp.1-7. ⟨10.1016/j.molbiopara.2011.04.006⟩, Molecular and Biochemical Parasitology, 2011, 179 (1), pp.1-7. ⟨10.1016/j.molbiopara.2011.04.006⟩
Publication Year :
2011
Publisher :
HAL CCSD, 2011.

Abstract

International audience; A single copy gene, encoding a protein highly similar to transketolase from other systems, was identified in the Trypanosoma brucei genome. The gene was expressed in E. coil and the purified protein demonstrated transketolase activity with Km values of 0.2 mM and 0.8 mM respectively for xylulose 5-phosphate and ribose 5-phosphate. A peroxisomal targeting signal (PTS-1) present at the C-terminus of the protein suggested a glycosomal localisation. However, subcellular localisation experiments revealed that while the protein was present in glycosomes it was found mainly within the cytosol and thus has a dual localisation. Transketolase activity was absent from the long slender bloodstream form of the parasite and the protein was not detectable in this life cycle stage, with the RNA present only at low abundance, indicating a strong differential regulation, being present predominantly in the procyclic form. The gene was knocked out from procyclic T. brucei and transketolase activity was lost but no growth phenotype was evident in the null mutants. Metabolite profiling to compare wild type and TKT null mutants revealed substantial increases in transketolase substrate metabolites coupled to loss of sedoheptulose 7-phosphate, a principal product of the transketolase reaction. (C) 2011 Elsevier B.V. All rights reserved.

Details

Language :
English
ISSN :
01666851
Database :
OpenAIRE
Journal :
Molecular and Biochemical Parasitology, Molecular and Biochemical Parasitology, Elsevier, 2011, 179 (1), pp.1-7. ⟨10.1016/j.molbiopara.2011.04.006⟩, Molecular and Biochemical Parasitology, 2011, 179 (1), pp.1-7. ⟨10.1016/j.molbiopara.2011.04.006⟩
Accession number :
edsair.doi.dedup.....ed9cef70bc8cc0854379e83db76f6993