alpha-Ketoglutaric acid

α-Ketoglutaric acid (2-oxoglutaric acid) is one of two ketone derivatives of glutaric acid. The term "ketoglutaric acid," when not further qualified, almost always refers to the alpha variant. β-Ketoglutaric acid varies only by the position of the ketone functional group, and is much less common.

α-Ketoglutaric acid[1]
Names
Preferred IUPAC name
2-Oxopentanedioic acid
Other names
2-Ketoglutaric acid
alpha-Ketoglutaric acid
2-Oxoglutaric acid
Oxoglutaric acid
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
DrugBank
ECHA InfoCard 100.005.756
KEGG
MeSH alpha-ketoglutaric+acid
PubChem CID
UNII
Properties
Chemical formula
C5H6O5
Molar mass 146.11 g/mol
Melting point 115 °C (239 °F; 388 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Its anion, α-ketoglutarate also called 2-oxoglutarate, is an important biological compound. It is the keto acid produced by deamination of glutamate, and is an intermediate in the Krebs cycle.

Functions

Alanine transaminase

The enzyme alanine transaminase converts α-ketoglutarate and L-alanine to L-glutamate and pyruvate, respectively, as a reversible process.

Krebs cycle

α-Ketoglutarate is a key intermediate in the Krebs cycle, coming after isocitrate and before succinyl CoA. Anaplerotic reactions can replenish the cycle at this juncture by synthesizing α-ketoglutarate from transamination of glutamate, or through action of glutamate dehydrogenase on glutamate.

Formation of amino acids

Glutamine is synthesized from glutamate by glutamine synthetase, which utilizes adenosine triphosphate to form glutamyl phosphate; this intermediate is attacked by ammonia as a nucleophile giving glutamine and inorganic phosphate. Proline, arginine, and lysine (in some organisms) are other amino acids synthesized as well.[2] These three amino acids derive from glutamate with the addition of further steps or enzymes to facilitate reactions.

Nitrogen transporter

Another function is to combine with nitrogen released in cells, therefore preventing nitrogen overload.

α-Ketoglutarate is one of the most important nitrogen transporters in metabolic pathways. The amino groups of amino acids are attached to it (by transamination) and carried to the liver where the urea cycle takes place.

α-Ketoglutarate is transaminated, along with glutamine, to form the excitatory neurotransmitter glutamate. Glutamate can then be decarboxylated (requiring vitamin B6) into the inhibitory neurotransmitter gamma-aminobutyric acid.

It is reported that high ammonia and/or high nitrogen levels may occur with high protein intake, excessive aluminum exposure, Reye's syndrome, cirrhosis, and urea cycle disorder.

It plays a role in detoxification of ammonia in brain.[3][4][5]

Relationship to molecular oxygen

Acting as a co-substrate for α-ketoglutarate-dependent hydroxylase, it also plays important function in oxidation reactions involving molecular oxygen.

Molecular oxygen (O2) directly oxidizes many compounds to produce useful products in an organism, such as antibiotics, in reactions catalyzed by oxygenases. In many oxygenases, α-ketoglutarate helps the reaction by being oxidized with the main substrate. EGLN1, one of the α-ketoglutarate-dependent oxygenases, is an O2 sensor, informing the organism the oxygen level in its environment.

In combination with molecular oxygen, alpha-ketoglutarate is one of the requirements for the hydroxylation of proline to hydroxyproline in the production of type 1 collagen.

Antioxidant

α-Ketoglutarate, which is released by several cell types, decreases the levels of hydrogen peroxide, and the α-ketoglutarate was depleted and converted to succinate in cell culture media.[6]

Longevity

A study released linked α-ketoglutarate with significantly increased lifespan in nematode worms. [7]

Immune regulation

A study showed that α-ketoglutarate promotes TH1 differentiation and depletion of glutamine (by depleting its metabolite, α-ketoglutarate favors treg (regulatory T-cell) differentiation. It might play a role in skewing the balance in favor of tregs in the setting of the amino acid deprivation that can be seen in the tumor microenvironment.[8]

Production

α-Ketoglutarate can be produced by:

Alpha-ketoglutarate can be used to produce:

  • Creatine-alpha ketoglutarate

Interactive pathway map

Click on genes, proteins and metabolites below to link to respective articles. [§ 1]

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go to HMDBgo to articlego to articlego to articlego to articlego to articlego to articlego to articlego to HMDBgo to articlego to HMDBgo to HMDBgo to articlego to HMDBgo to articlego to articlego to articlego to articlego to articlego to WikiPathways
|{{{bSize}}}px|alt=TCA Cycle edit]]
TCA Cycle edit
  1. The interactive pathway map can be edited at WikiPathways: "TCACycle_WP78".

See also

  • 2OG-dependent dioxygenases

References

  1. Merck Index, 13th Edition, 5320.
  2. Ledwidge, Richard; Blanchard, John S. (1999). "The Dual Biosynthetic Capability of N-Acetylornithine Aminotransferase in Arginine and Lysine Biosynthesis†". Biochemistry. 38 (10): 3019–3024. doi:10.1021/bi982574a. PMID 10074354.
  3. "Does infectious fever relieve autistic behavior by releasing glutamine from skeletal muscles as provisional fuel?". Archived from the original on 2014-05-19. Retrieved 2014-05-19.
  4. Ott, P; Clemmesen, O; Larsen, FS (Jul 2005). "Cerebral metabolic disturbances in the brain during acute liver failure: from hyperammonemia to energy failure and proteolysis". Neurochemistry International. 47 (1–2): 13–8. doi:10.1016/j.neuint.2005.04.002. PMID 15921824.
  5. Hares, P; James, IM; Pearson, RM (May–Jun 1978). "Effect of ornithine alpha ketoglutarate (OAKG) on the response of brain metabolism to hypoxia in the dog". Stroke: A Journal of Cerebral Circulation. 9 (3): 222–4. doi:10.1161/01.STR.9.3.222. PMID 644619.
  6. Long, L; Halliwell, B (2011). "Artefacts in cell culture: α-Ketoglutarate can scavenge hydrogen peroxide generated by ascorbate and epigallocatechin gallate in cell culture media". Biochemical and Biophysical Research Communications. 406 (1): 20–24. doi:10.1016/j.bbrc.2011.01.091. PMID 21281600.
  7. Chin, RM; Fu, X; Pai, MY; Vergnes, L; Hwang, H; Deng, G; Diep, S; Lomenick, B; Meli, VS; Monsalve, GC; Hu, E; Whelan, SA; Wang, JX; Jung, G; Solis, GM; Fazlollahi, F; Kaweeteerawat, C; Quach, A; Nili, M; Krall, AS; Godwin, HA; Chang, HR; Faull, KF; Guo, F; Jiang, M; Trauger, SA; Saghatelian, A; Braas, D; Christofk, HR; Clarke, CF; Teitell, MA; Petrascheck, M; Reue, K; Jung, ME; Frand, AR; Huang, J (2014). "The metabolite α-ketoglutarate extends lifespan by inhibiting ATP synthase and TOR". Nature. 510 (7505): 397–401. Bibcode:2014Natur.510..397C. doi:10.1038/nature13264. PMC 4263271. PMID 24828042.
  8. Klysz, Dorota; Tai, Xuguang (29 September 2015). "Glutamine-dependent α-ketoglutarate production regulates the balance between T helper 1 cell and regulatory T cell generation". Science Signaling. 8 (396): ra97. doi:10.1126/scisignal.aab2610. PMID 26420908.
  9. Richard, Peter; Hilditch, Satu (2009). "d-Galacturonic acid catabolism in microorganisms and its biotechnological relevance". Applied Microbiology and Biotechnology. 82 (4): 597–604. doi:10.1007/s00253-009-1870-6. ISSN 0175-7598. PMID 19159926.
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