Literature DB >> 18430732

Glucose-induced remodeling of intermediary and energy metabolism in procyclic Trypanosoma brucei.

Virginie Coustou1, Marc Biran, Marc Breton, Fabien Guegan, Loïc Rivière, Nicolas Plazolles, Derek Nolan, Michael P Barrett, Jean-Michel Franconi, Frédéric Bringaud.   

Abstract

The procyclic form of Trypanosoma brucei is a parasitic protozoan that normally dwells in the midgut of its insect vector. In vitro, this parasite prefers d-glucose to l -proline as a carbon source, although this amino acid is the main carbon source available in its natural habitat. Here, we investigated how l -proline is metabolized in glucose-rich and glucose-depleted conditions. Analysis of the excreted end products of (13)C-enriched l -proline metabolism showed that the amino acid is converted into succinate or l -alanine depending on the presence or absence of d-glucose, respectively. The fact that the pathway of l -proline metabolism was truncated in glucose-rich conditions was confirmed by the analysis of 13 separate RNA interference-harboring or knock-out cell lines affecting different steps of this pathway. For instance, RNA interference studies revealed the loss of succinate dehydrogenase activity to be conditionally lethal only in the absence of d-glucose, confirming that in glucose-depleted conditions, l -proline needs to be converted beyond succinate. In addition, depletion of the F(0)/F(1)-ATP synthase activity by RNA interference led to cell death in glucose-depleted medium, but not in glucose-rich medium. This implies that, in the presence of d-glucose, the importance of the F(0)/F(1)-ATP synthase is diminished and ATP is produced by substrate level phosphorylation. We conclude that trypanosomes develop an elaborate adaptation of their energy production pathways in response to carbon source availability.

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Year:  2008        PMID: 18430732     DOI: 10.1074/jbc.M709592200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  55 in total

1.  Isotopomer profiling of Leishmania mexicana promastigotes reveals important roles for succinate fermentation and aspartate uptake in tricarboxylic acid cycle (TCA) anaplerosis, glutamate synthesis, and growth.

Authors:  Eleanor C Saunders; William W Ng; Jennifer M Chambers; Milica Ng; Thomas Naderer; Jens O Krömer; Vladimir A Likic; Malcolm J McConville
Journal:  J Biol Chem       Date:  2011-06-02       Impact factor: 5.157

2.  ATP synthesis-coupled and -uncoupled acetate production from acetyl-CoA by mitochondrial acetate:succinate CoA-transferase and acetyl-CoA thioesterase in Trypanosoma.

Authors:  Yoann Millerioux; Pauline Morand; Marc Biran; Muriel Mazet; Patrick Moreau; Marion Wargnies; Charles Ebikeme; Kamel Deramchia; Lara Gales; Jean-Charles Portais; Michael Boshart; Jean-Michel Franconi; Frédéric Bringaud
Journal:  J Biol Chem       Date:  2012-04-02       Impact factor: 5.157

3.  Host-parasite interactions revealed by Plasmodium falciparum metabolomics.

Authors:  Kellen L Olszewski; Joanne M Morrisey; Daniel Wilinski; James M Burns; Akhil B Vaidya; Joshua D Rabinowitz; Manuel Llinás
Journal:  Cell Host Microbe       Date:  2009-02-19       Impact factor: 21.023

4.  pH regulation in glycosomes of procyclic form Trypanosoma brucei.

Authors:  Sheng Lin; Charles Voyton; Meredith T Morris; P Christine Ackroyd; James C Morris; Kenneth A Christensen
Journal:  J Biol Chem       Date:  2017-03-27       Impact factor: 5.157

5.  Antimalarial drug targets in Plasmodium falciparum predicted by stage-specific metabolic network analysis.

Authors:  Carola Huthmacher; Andreas Hoppe; Sascha Bulik; Hermann-Georg Holzhütter
Journal:  BMC Syst Biol       Date:  2010-08-31

6.  Functional characterization of TbMCP5, a conserved and essential ADP/ATP carrier present in the mitochondrion of the human pathogen Trypanosoma brucei.

Authors:  Priscila Peña-Diaz; Ludovic Pelosi; Charles Ebikeme; Claudia Colasante; Fei Gao; Frederic Bringaud; Frank Voncken
Journal:  J Biol Chem       Date:  2012-10-16       Impact factor: 5.157

7.  Acetate produced in the mitochondrion is the essential precursor for lipid biosynthesis in procyclic trypanosomes.

Authors:  Loïc Rivière; Patrick Moreau; Stefan Allmann; Matthias Hahn; Marc Biran; Nicolas Plazolles; Jean-Michel Franconi; Michael Boshart; Frédéric Bringaud
Journal:  Proc Natl Acad Sci U S A       Date:  2009-07-22       Impact factor: 11.205

8.  Proteomic and network analysis characterize stage-specific metabolism in Trypanosoma cruzi.

Authors:  Seth B Roberts; Jennifer L Robichaux; Arvind K Chavali; Patricio A Manque; Vladimir Lee; Ana M Lara; Jason A Papin; Gregory A Buck
Journal:  BMC Syst Biol       Date:  2009-05-16

9.  Digital gene expression analysis of two life cycle stages of the human-infective parasite, Trypanosoma brucei gambiense reveals differentially expressed clusters of co-regulated genes.

Authors:  Nicola J Veitch; Paul C D Johnson; Urmi Trivedi; Sandra Terry; David Wildridge; Annette MacLeod
Journal:  BMC Genomics       Date:  2010-02-22       Impact factor: 3.969

10.  The F(0)F(1)-ATP synthase complex contains novel subunits and is essential for procyclic Trypanosoma brucei.

Authors:  Alena Zíková; Achim Schnaufer; Rachel A Dalley; Aswini K Panigrahi; Kenneth D Stuart
Journal:  PLoS Pathog       Date:  2009-05-15       Impact factor: 6.823

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