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丙酮酸磷酸二激酶在布氏锥虫前循环型糖体ATP/ADP平衡维持中的作用。

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

作者信息

Deramchia Kamel, Morand Pauline, Biran Marc, Millerioux Yoann, Mazet Muriel, Wargnies Marion, Franconi Jean-Michel, Bringaud Frédéric

机构信息

From the Centre de Résonance Magnétique des Systèmes Biologiques, Université de Bordeaux, CNRS UMR-5536, 146 rue Léo Saignat, 33076 Bordeaux Cedex, France.

From the Centre de Résonance Magnétique des Systèmes Biologiques, Université de Bordeaux, CNRS UMR-5536, 146 rue Léo Saignat, 33076 Bordeaux Cedex, France

出版信息

J Biol Chem. 2014 Jun 20;289(25):17365-78. doi: 10.1074/jbc.M114.567230. Epub 2014 May 2.

Abstract

Trypanosoma brucei belongs to a group of protists that sequester the first six or seven glycolytic steps inside specialized peroxisomes, named glycosomes. Because of the glycosomal membrane impermeability to nucleotides, ATP molecules consumed by the first glycolytic steps need to be regenerated in the glycosomes by kinases, such as phosphoenolpyruvate carboxykinase (PEPCK). The glycosomal pyruvate phosphate dikinase (PPDK), which reversibly converts phosphoenolpyruvate into pyruvate, could also be involved in this process. To address this question, we analyzed the metabolism of the main carbon sources used by the procyclic trypanosomes (glucose, proline, and threonine) after deletion of the PPDK gene in the wild-type (Δppdk) and PEPCK null (Δppdk/Δpepck) backgrounds. The rate of acetate production from glucose is 30% reduced in the Δppdk mutant, whereas threonine-derived acetate production is not affected, showing that PPDK function in the glycolytic direction with production of ATP in the glycosomes. The Δppdk/Δpepck mutant incubated in glucose as the only carbon source showed a 3.8-fold reduction of the glycolytic rate compared with the Δpepck mutant, as a consequence of the imbalanced glycosomal ATP/ADP ratio. The role of PPDK in maintenance of the ATP/ADP balance was confirmed by expressing the glycosomal phosphoglycerate kinase (PGKC) in the Δppdk/Δpepck cell line, which restored the glycolytic flux. We also observed that expression of PGKC is lethal for procyclic trypanosomes, as a consequence of ATP depletion, due to glycosomal relocation of cytosolic ATP production. This illustrates the key roles played by glycosomal and cytosolic kinases, including PPDK, to maintain the cellular ATP/ADP homeostasis.

摘要

布氏锥虫属于一类原生生物,它们将糖酵解的前六个或七个步骤隔离在特殊的过氧化物酶体(称为糖体)中。由于糖体膜对核苷酸不渗透,糖酵解前几步消耗的ATP分子需要由激酶(如磷酸烯醇丙酮酸羧激酶(PEPCK))在糖体中再生。糖体丙酮酸磷酸二激酶(PPDK)可将磷酸烯醇丙酮酸可逆地转化为丙酮酸,也可能参与这一过程。为了解决这个问题,我们分析了在野生型(Δppdk)和PEPCK缺失型(Δppdk/Δpepck)背景下删除PPDK基因后,前循环锥虫使用的主要碳源(葡萄糖、脯氨酸和苏氨酸)的代谢情况。在Δppdk突变体中,由葡萄糖产生乙酸盐的速率降低了30%,而苏氨酸衍生的乙酸盐产生不受影响,这表明PPDK在糖体中沿糖酵解方向发挥作用并产生ATP。与Δpepck突变体相比,以葡萄糖作为唯一碳源培养的Δppdk/Δpepck突变体的糖酵解速率降低了3.8倍,这是糖体中ATP/ADP比例失衡的结果。通过在Δppdk/Δpepck细胞系中表达糖体磷酸甘油酸激酶(PGKC),恢复了糖酵解通量,从而证实了PPDK在维持ATP/ADP平衡中的作用。我们还观察到,由于胞质ATP产生在糖体中的重新定位导致ATP耗竭,PGKC的表达对前循环锥虫是致命的。这说明了包括PPDK在内的糖体和胞质激酶在维持细胞ATP/ADP稳态中所起的关键作用。

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本文引用的文献

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Flux Analysis of the Trypanosoma brucei Glycolysis Based on a Multiobjective-Criteria Bioinformatic Approach.
Adv Bioinformatics. 2012;2012:159423. doi: 10.1155/2012/159423. Epub 2012 Oct 13.
6
Multiple roles of proline transport and metabolism in trypanosomatids.
Front Biosci (Landmark Ed). 2012 Jan 1;17(1):349-74. doi: 10.2741/3931.
7
When, how and why glycolysis became compartmentalised in the Kinetoplastea. A new look at an ancient organelle.
Int J Parasitol. 2012 Jan;42(1):1-20. doi: 10.1016/j.ijpara.2011.10.007. Epub 2011 Nov 22.
8
Concentration Measurement by Proton NMR Using the ERETIC Method.
Anal Chem. 1999 Jul 1;71(13):2554-7. doi: 10.1021/ac981422i.
9
The exopolyphosphatase TbrPPX1 of Trypanosoma brucei.
BMC Microbiol. 2011 Jan 6;11:4. doi: 10.1186/1471-2180-11-4.

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