Literature DB >> 22142562

When, how and why glycolysis became compartmentalised in the Kinetoplastea. A new look at an ancient organelle.

Melisa Gualdrón-López1, Ana Brennand, Véronique Hannaert, Wilfredo Quiñones, Ana J Cáceres, Frédéric Bringaud, Juan Luis Concepción, Paul A M Michels.   

Abstract

A characteristic, well-studied feature of the pathogenic protists belonging to the family Trypanosomatidae is the compartmentalisation of the major part of the glycolytic pathway in peroxisome-like organelles, hence designated glycosomes. Such organelles containing glycolytic enzymes appear to be present in all members of the Kinetoplastea studied, and have recently also been detected in a representative of the Diplonemida, but they are absent from the Euglenida. Glycosomes therefore probably originated in a free-living, common ancestor of the Kinetoplastea and Diplonemida. The initial sequestering of glycolytic enzymes inside peroxisomes may have been the result of a minor mistargeting of proteins, as generally observed in eukaryotic cells, followed by preservation and its further expansion due to the selective advantage of this specific form of metabolic compartmentalisation. This selective advantage may have been a largely increased metabolic flexibility, allowing the organisms to adapt more readily and efficiently to different environmental conditions. Further evolution of glycosomes involved, in different taxonomic lineages, the acquisition of additional enzymes and pathways - often participating in core metabolic processes - as well as the loss of others. The acquisitions may have been promoted by the sharing of cofactors and crucial metabolites between different pathways, thus coupling different redox processes and catabolic and anabolic pathways within the organelle. A notable loss from the Trypanosomatidae concerned a major part of the typical peroxisomal H(2)O(2)-linked metabolism. We propose that the compartmentalisation of major parts of the enzyme repertoire involved in energy, carbohydrate and lipid metabolism has contributed to the multiple development of parasitism, and its elaboration to complicated life cycles involving consecutive different hosts, in the protists of the Kinetoplastea clade.
Copyright © 2011 Australian Society for Parasitology Inc. Published by Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 22142562     DOI: 10.1016/j.ijpara.2011.10.007

Source DB:  PubMed          Journal:  Int J Parasitol        ISSN: 0020-7519            Impact factor:   3.981


  36 in total

Review 1.  Biochemistry and evolution of anaerobic energy metabolism in eukaryotes.

Authors:  Miklós Müller; Marek Mentel; Jaap J van Hellemond; Katrin Henze; Christian Woehle; Sven B Gould; Re-Young Yu; Mark van der Giezen; Aloysius G M Tielens; William F Martin
Journal:  Microbiol Mol Biol Rev       Date:  2012-06       Impact factor: 11.056

Review 2.  Purine salvage in Leishmania: complex or simple by design?

Authors:  Jan M Boitz; Buddy Ullman; Armando Jardim; Nicola S Carter
Journal:  Trends Parasitol       Date:  2012-06-20

3.  N-Terminal Presequence-Independent Import of Phosphofructokinase into Hydrogenosomes of Trichomonas vaginalis.

Authors:  Petr Rada; Abhijith Radhakrishna Makki; Verena Zimorski; Sriram Garg; Vladimír Hampl; Ivan Hrdý; Sven B Gould; Jan Tachezy
Journal:  Eukaryot Cell       Date:  2015-10-16

Review 4.  The neomuran revolution and phagotrophic origin of eukaryotes and cilia in the light of intracellular coevolution and a revised tree of life.

Authors:  Thomas Cavalier-Smith
Journal:  Cold Spring Harb Perspect Biol       Date:  2014-09-02       Impact factor: 10.005

5.  Contribution of pyruvate phosphate dikinase in the maintenance of the glycosomal ATP/ADP balance in the Trypanosoma brucei procyclic form.

Authors:  Kamel Deramchia; Pauline Morand; Marc Biran; Yoann Millerioux; Muriel Mazet; Marion Wargnies; Jean-Michel Franconi; Frédéric Bringaud
Journal:  J Biol Chem       Date:  2014-05-02       Impact factor: 5.157

6.  Differential remodelling of peroxisome function underpins the environmental and metabolic adaptability of diplonemids and kinetoplastids.

Authors:  Jorge Morales; Muneaki Hashimoto; Tom A Williams; Hiroko Hirawake-Mogi; Takashi Makiuchi; Akiko Tsubouchi; Naoko Kaga; Hikari Taka; Tsutomu Fujimura; Masato Koike; Toshihiro Mita; Frédéric Bringaud; Juan L Concepción; Tetsuo Hashimoto; T Martin Embley; Takeshi Nara
Journal:  Proc Biol Sci       Date:  2016-05-11       Impact factor: 5.349

Review 7.  Trypanosoma brucei: Metabolomics for analysis of cellular metabolism and drug discovery.

Authors:  Fanta Fall; Lucia Mamede; Laura Schioppa; Allison Ledoux; Pascal De Tullio; Paul Michels; Michel Frédérich; Joëlle Quetin-Leclercq
Journal:  Metabolomics       Date:  2022-03-19       Impact factor: 4.290

8.  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

9.  Role of cytosolic glyceraldehyde-3-phosphate dehydrogenase in visceral organ infection by Leishmania donovani.

Authors:  Wen-Wei Zhang; Laura-Isobel McCall; Greg Matlashewski
Journal:  Eukaryot Cell       Date:  2012-11-02

10.  Channel-forming activities in the glycosomal fraction from the bloodstream form of Trypanosoma brucei.

Authors:  Melisa Gualdron-López; Miia H Vapola; Ilkka J Miinalainen; J Kalervo Hiltunen; Paul A M Michels; Vasily D Antonenkov
Journal:  PLoS One       Date:  2012-04-10       Impact factor: 3.240

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