Probing the Metabolic Network in Bloodstream-Form Trypanosoma brucei Using Untargeted Metabolomics with Stable Isotope Labelled Glucose
Glycerol
0301 basic medicine
570
/dk/atira/pure/subjectarea/asjc/1300/1311
/dk/atira/pure/subjectarea/asjc/1300/1312
/dk/atira/pure/subjectarea/asjc/2400/2404
QH301-705.5
/dk/atira/pure/subjectarea/asjc/2400/2405
Immunology
/dk/atira/pure/subjectarea/asjc/2400/2406
Trypanosoma brucei brucei
Succinic Acid
610
Microbiology
RS
Pentose Phosphate Pathway
03 medical and health sciences
Pharmacy and materia medica
Virology
Genetics
Animals
Metabolomics
[SDV.MP.PAR]Life Sciences [q-bio]/Microbiology and Parasitology/Parasitology
/dk/atira/pure/subjectarea/asjc/2400/2403
Biology (General)
Molecular Biology
Cells, Cultured
RC581-607
3. Good health
Glucose
Parasitology
Immunologic diseases. Allergy
Oxidation-Reduction
Metabolic Networks and Pathways
Research Article
DOI:
10.1371/journal.ppat.1004689
Publication Date:
2015-03-16T18:14:04Z
AUTHORS (17)
ABSTRACT
Metabolomics coupled with heavy-atom isotope-labelled glucose has been used to probe the metabolic pathways active in cultured bloodstream form trypomastigotes of Trypanosoma brucei, a parasite responsible for human African trypanosomiasis. Glucose enters many branches of metabolism beyond glycolysis, which has been widely held to be the sole route of glucose metabolism. Whilst pyruvate is the major end-product of glucose catabolism, its transamination product, alanine, is also produced in significant quantities. The oxidative branch of the pentose phosphate pathway is operative, although the non-oxidative branch is not. Ribose 5-phosphate generated through this pathway distributes widely into nucleotide synthesis and other branches of metabolism. Acetate, derived from glucose, is found associated with a range of acetylated amino acids and, to a lesser extent, fatty acids; while labelled glycerol is found in many glycerophospholipids. Glucose also enters inositol and several sugar nucleotides that serve as precursors to macromolecule biosynthesis. Although a Krebs cycle is not operative, malate, fumarate and succinate, primarily labelled in three carbons, were present, indicating an origin from phosphoenolpyruvate via oxaloacetate. Interestingly, the enzyme responsible for conversion of phosphoenolpyruvate to oxaloacetate, phosphoenolpyruvate carboxykinase, was shown to be essential to the bloodstream form trypanosomes, as demonstrated by the lethal phenotype induced by RNAi-mediated downregulation of its expression. In addition, glucose derivatives enter pyrimidine biosynthesis via oxaloacetate as a precursor to aspartate and orotate.
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