Metabolic control exerted by the 2-oxoglutarate dehydrogenase reaction: a cross-kingdom comparison of the crossroad between energy production and nitrogen assimilation

被引:109
作者
Bunik, Victoria I. [1 ]
Fernie, Alisdair R. [2 ]
机构
[1] Moscow MV Lomonosov State Univ, AN Belozersky Inst Physicochem Biol, Moscow 119992, Russia
[2] Max Planck Inst Mol Planzenphysiol, D-14476 Potsdam, Germany
关键词
gamma-aminobutytic acid (GABA); excitotoxicity; metabolic control; nitrogen assimilation; 2-oxoglutarate dehydrogenase (OGDH); thiamine deficiency; ALPHA-KETOGLUTARATE-DEHYDROGENASE; CITRIC-ACID CYCLE; PYRUVATE-DEHYDROGENASE; ESCHERICHIA-COLI; OXOGLUTARATE DEHYDROGENASE; ISOCITRATE DEHYDROGENASE; THIAMINE PYROPHOSPHATE; DIHYDROLIPOAMIDE SUCCINYLTRANSFERASE; PHOTOSYNTHETIC PERFORMANCE; OXIDATIVE DECARBOXYLATION;
D O I
10.1042/BJ20090722
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mechanism-based inhibitors and both forward and reverse genetics have proved to be essential tools in revealing roles for specific enzymatic processes in cellular function. Here, we review experimental studies aimed at assessing the impact of OG (2-oxoglutarate) oxidative decarboxylation oil basic cellular activities in a number of biological systems. After summarizing the catalytic and regulatory properties of the OGDHC (OG dehydrogenase complex), we describe the evidence that has been accrued on its cellular role. We demonstrate an essential role of this enzyme in metabolic control in a wide range of organisms. Targeting this enzyme in different cells and tissues, mainly by its specific inhibitors, effects changes in a number of basic functions, such as mitochondrial potential, tissue respiration, ROS (reactive oxygen species) production, nitrogen metabolism, glutamate signalling and survival, Supporting the notion that the evolutionary conserved reaction of OG degradation is required for metabolic adaptation. In particular, regulation of OGDHC under stress conditions may be essential to overcome glutamate excitotoxicity in neurons or affect the wound response in plants. Thus, apart from its role in producing energy, the flux through OGDHC significantly affects nitrogen' assimilation and amino acid metabolism, whereas the side reactions of OGDHC, such as ROS production and the carboligase reaction, have biological functions in signalling and glyoxylate utilization. Our current view on the role of OGDHC reaction in various processes within complex biological systems allows us a far greater fundamental understanding of metabolic regulation and also opens up new opportunities for us to address both biotechnological and medical challenges.
引用
收藏
页码:405 / 421
页数:17
相关论文
共 172 条
[1]   CONTROL OF CITRIC ACID CYCLE BY GLYOXYLATE - MECHANISM OF INHIBITION OF OXOGLUTARATE DEHYDROGENASE, ISOCITRATE DEHYDROGENASE AND ACONITATE HYDRATASE [J].
ADINOLFI, A ;
MORATTI, R ;
OLEZZA, S ;
RUFFO, A .
BIOCHEMICAL JOURNAL, 1969, 114 (03) :513-&
[2]  
ADINOLFI A, 1967, BIOCHEM J, V104, pP50
[3]   Global organization of metabolic fluxes in the bacterium Escherichia coli [J].
Almaas, E ;
Kovács, B ;
Vicsek, T ;
Oltvai, ZN ;
Barabási, AL .
NATURE, 2004, 427 (6977) :839-843
[4]  
AMARASINGHAM CR, 1965, J BIOL CHEM, V240, P3664
[5]   Identification of 315 genes essential for early zebrafish development [J].
Amsterdam, A ;
Nissen, RM ;
Sun, ZX ;
Swindell, EC ;
Farrington, S ;
Hopkins, N .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (35) :12792-12797
[6]   Inhibition of 2-Oxoglutarate Dehydrogenase in Potato Tuber Suggests the Enzyme Is Limiting for Respiration and Confirms Its Importance in Nitrogen Assimilation [J].
Araujo, Wagner L. ;
Nunes-Nesi, Adriano ;
Trenkamp, Sandra ;
Bunik, Victoria I. ;
Fernie, Alisdair R. .
PLANT PHYSIOLOGY, 2008, 148 (04) :1782-1796
[7]   A thiamin-bound, pre-decarboxylation reaction intermediate analogue in the pyruvate dehydrogenase E1 subunit induces large scale disorder-to-order transformations in the enzyme and reveals novel structural features in the covalently bound adduct [J].
Arjunan, Palaniappa ;
Sax, Martin ;
Brunskill, Andrew ;
Chandrasekhar, Krishnamoorthy ;
Nemeria, Natalia ;
Zhang, Sheng ;
Jordan, Frank ;
Furey, William .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (22) :15296-15303
[8]   Thioredoxin links redox to the regulation of fundamental processes of plant mitochondria [J].
Balmer, Y ;
Vensel, WH ;
Tanaka, CK ;
Hurkman, WJ ;
Gelhaye, E ;
Rouhier, N ;
Jacquot, JP ;
Manieri, W ;
Schüurmann, P ;
Droux, M ;
Buchanan, BB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (08) :2642-2647
[9]   Kinetics and specificity of reductive acylation of mild-type and mutated lipoyl domains of 2-oxo-acid dehydrogenase complexes from Azotobacter vinelandii [J].
Berg, A ;
Westphal, AH ;
Bosma, HJ ;
De Kok, A .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1998, 252 (01) :45-50
[10]   Discovery of a natural thiamine adenine nucleotide [J].
Bettendorff, Lucien ;
Wirtzfeld, Barbara ;
Makarchikov, Alexander F. ;
Mazzucchelli, Gabriel ;
Frederich, Michel ;
Gigliobianco, Tiziana ;
Gangolf, Marjorie ;
De Pauw, Edwin ;
Angenot, Luc ;
Wins, Pierre .
NATURE CHEMICAL BIOLOGY, 2007, 3 (04) :211-212