Pentose phosphate pathway

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The pentose phosphate pathway Pentose Phosphate Pathway.png
The pentose phosphate pathway

The pentose phosphate pathway (also called the phosphogluconate pathway and the hexose monophosphate shunt and the HMP Shunt) is a metabolic pathway parallel to glycolysis. [1] It generates NADPH and pentoses (5-carbon sugars) as well as ribose 5-phosphate, a precursor for the synthesis of nucleotides. [1] While the pentose phosphate pathway does involve oxidation of glucose, its primary role is anabolic rather than catabolic. The pathway is especially important in red blood cells (erythrocytes). The reactions of the pathway were elucidated in the early 1950s by Bernard Horecker and co-workers. [2] [3]

Contents

There are two distinct phases in the pathway. The first is the oxidative phase, in which NADPH is generated, and the second is the non-oxidative synthesis of 5-carbon sugars. For most organisms, the pentose phosphate pathway takes place in the cytosol; in plants, most steps take place in plastids. [4]

Like glycolysis, the pentose phosphate pathway appears to have a very ancient evolutionary origin. The reactions of this pathway are mostly enzyme-catalyzed in modern cells, however, they also occur non-enzymatically under conditions that replicate those of the Archean ocean, and are catalyzed by metal ions, particularly ferrous ions (Fe(II)). [5] This suggests that the origins of the pathway could date back to the prebiotic world.

Outcome

The primary results of the pathway are:

Aromatic amino acids, in turn, are precursors for many biosynthetic pathways, including the lignin in wood.[ citation needed ]

Dietary pentose sugars derived from the digestion of nucleic acids may be metabolized through the pentose phosphate pathway, and the carbon skeletons of dietary carbohydrates may be converted into glycolytic/gluconeogenic intermediates.

In mammals, the PPP occurs exclusively in the cytoplasm. In humans, it is found to be most active in the liver, mammary glands, and adrenal cortex.[ citation needed ] The PPP is one of the three main ways the body creates molecules with reducing power, accounting for approximately 60% of NADPH production in humans.[ citation needed ]

One of the uses of NADPH in the cell is to prevent oxidative stress. It reduces glutathione via glutathione reductase, which converts reactive H2O2 into H2O by glutathione peroxidase. If absent, the H2O2 would be converted to hydroxyl free radicals by Fenton chemistry, which can attack the cell. Erythrocytes, for example, generate a large amount of NADPH through the pentose phosphate pathway to use in the reduction of glutathione.

Hydrogen peroxide is also generated for phagocytes in a process often referred to as a respiratory burst. [6]

Phases

Oxidative phase

In this phase, two molecules of NADP + are reduced to NADPH, utilizing the energy from the conversion of glucose-6-phosphate into ribulose 5-phosphate.

Oxidative phase of pentose phosphate pathway. Glucose-6-phosphate (1), 6-phosphoglucono-d-lactone (2), 6-phosphogluconate (3), ribulose 5-phosphate (4) Ox Pentose phosphate pathway.svg
Oxidative phase of pentose phosphate pathway.
Glucose-6-phosphate (1), 6-phosphoglucono-δ-lactone (2), 6-phosphogluconate (3), ribulose 5-phosphate (4)

The entire set of reactions can be summarized as follows:

ReactantsProductsEnzymeDescription
Glucose 6-phosphate + NADP+→ 6-phosphoglucono-δ-lactone + NADPH glucose 6-phosphate dehydrogenase Dehydrogenation. The hydroxyl on carbon 1 of glucose 6-phosphate turns into a carbonyl, generating a lactone, and, in the process, NADPH is generated.
6-phosphoglucono-δ-lactone + H2O→ 6-phosphogluconate + H+ 6-phosphogluconolactonase Hydrolysis
6-phosphogluconate + NADP+→ ribulose 5-phosphate + NADPH + CO2 6-phosphogluconate dehydrogenase Oxidative decarboxylation. NADP+ is the electron acceptor, generating another molecule of NADPH, a CO2, and ribulose 5-phosphate.

The overall reaction for this process is:

Glucose 6-phosphate + 2 NADP+ + H2O → ribulose 5-phosphate + 2 NADPH + 2 H+ + CO2

Non-oxidative phase

The pentose phosphate pathway's nonoxidative phase Nichtox Pentosephosphatweg.png
The pentose phosphate pathway's nonoxidative phase
ReactantsProductsEnzymes
ribulose 5-phosphate → ribose 5-phosphate ribose-5-phosphate isomerase
ribulose 5-phosphate → xylulose 5-phosphate ribulose 5-phosphate 3-epimerase
xylulose 5-phosphate + ribose 5-phosphate → glyceraldehyde 3-phosphate + sedoheptulose 7-phosphate transketolase
sedoheptulose 7-phosphate + glyceraldehyde 3-phosphate → erythrose 4-phosphate + fructose 6-phosphate transaldolase
xylulose 5-phosphate + erythrose 4-phosphate → glyceraldehyde 3-phosphate + fructose 6-phosphate transketolase

Net reaction: 3 ribulose-5-phosphate → 1 ribose-5-phosphate + 2 xylulose-5-phosphate → 2 fructose-6-phosphate + glyceraldehyde-3-phosphate

Regulation

Glucose-6-phosphate dehydrogenase is the rate-controlling enzyme of this pathway[ citation needed ]. It is allosterically stimulated by NADP+ and strongly inhibited by NADPH. [7] The ratio of NADPH:NADP+ is the primary mode of regulation for the enzyme and is normally about 100:1 in liver cytosol[ citation needed ]. This makes the cytosol a highly-reducing environment. An NADPH-utilizing pathway forms NADP+, which stimulates Glucose-6-phosphate dehydrogenase to produce more NADPH. This step is also inhibited by acetyl CoA.[ citation needed ]

G6PD activity is also post-translationally regulated by cytoplasmic deacetylase SIRT2. SIRT2-mediated deacetylation and activation of G6PD stimulates oxidative branch of PPP to supply cytosolic NADPH to counteract oxidative damage or support de novo lipogenesis. [8] [9]

Erythrocytes

Several deficiencies in the level of activity (not function) of glucose-6-phosphate dehydrogenase have been observed to be associated with resistance to the malarial parasite Plasmodium falciparum among individuals of Mediterranean and African descent. The basis for this resistance may be a weakening of the red cell membrane (the erythrocyte is the host cell for the parasite) such that it cannot sustain the parasitic life cycle long enough for productive growth. [10]

See also

Related Research Articles

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References

  1. 1 2 Alfarouk KO, Ahmed SB, Elliott RL, et al. (2020). "The Pentose Phosphate Pathway Dynamics in Cancer and Its Dependency on Intracellular pH". Metabolites. 10: 285. doi: 10.3390/metabo10070285 . PMC   7407102 . PMID   32664469.
  2. ↑ Horecker BL, Smyrniotis PZ, Seegmiller JE (1951). "The enzymatic conversion of 6-phosphogluconate to ribulose-5-phosphate and ribose-5-phosphate". J. Biol. Chem. 193 (1): 383–396. doi: 10.1016/S0021-9258(19)52464-4 . PMID   14907726.
  3. ↑ Horecker BL (2002). "The pentose phosphate pathway". J. Biol. Chem. 277 (50): 47965–47971. doi: 10.1074/jbc.X200007200 . PMID   12403765.
  4. ↑ Kruger NJ, von Schaewen A (June 2003). "The oxidative pentose phosphate pathway: structure and organisation". Current Opinion in Plant Biology. 6 (3): 236–246. Bibcode:2003COPB....6..236K. doi:10.1016/S1369-5266(03)00039-6. PMID   12753973.
  5. ↑ Keller MA, Turchyn AV, Ralser M (25 April 2014). "Non-enzymatic glycolysis and pentose phosphate pathway-like reactions in a plausible Archean ocean". Molecular Systems Biology. 10 (4): 725. doi:10.1002/msb.20145228. PMC   4023395 . PMID   24771084.
  6. ↑ Immunology at MCG 1/cytotox
  7. ↑ Voet Donald, Voet Judith G (2011). Biochemistry (4th ed.). John Wiley & Sons. p. 894. ISBN   978-0-470-57095-1.
  8. ↑ Wang YP, Zhou LS, Zhao YZ, Wang SW, Chen LL, Liu LX, Ling ZQ, Hu FJ, Sun YP, Zhang JY, Yang C, Yang Y, Xiong Y, Guan KL, Ye D (June 2014). "Regulation of G6PD acetylation by SIRT2 and KAT9 modulates NADPH homeostasis and cell survival during oxidative stress". EMBO Journal. 33 (12): 1304–20. doi:10.1002/embj.201387224. PMC   4194121 . PMID   24769394.
  9. ↑ Xu SN, Wang TS, Li X, Wang YP (Sep 2016). "SIRT2 activates G6PD to enhance NADPH production and promote leukaemia cell proliferation". Sci Rep. 6: 32734. Bibcode:2016NatSR...632734X. doi:10.1038/srep32734. PMC   5009355 . PMID   27586085.
  10. ↑ Cappadoro M, Giribaldi G, O'Brien E, et al. (October 1998). "Early phagocytosis of glucose-6-phosphate dehydrogenase (G6PD)-deficient erythrocytes parasitized by Plasmodium falciparum may explain malaria protection in G6PD deficiency". Blood. 92 (7): 2527–34. doi: 10.1182/blood.V92.7.2527 . PMID   9746794.
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