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The pentose phosphate pathway (also called the phosphogluconate pathway and the hexose monophosphate shunt) is a process that generates NADPH and pentoses (5-carbon sugars). There are two distinct phases in the pathway. The first is the oxidative phase, in which NADPH is generated, and the second is the nonoxidative synthesis of 5-carbon sugars. This pathway is an alternative to glycolysis. While it does involve oxidation of glucose, its primary role is anabolic rather than catabolic. For most organisms, it takes place in the cytosol; in plants, most steps take place in plastids.[1]
Contents
1 Outcome 2 Phases 2.1 Oxidative phase 2.2 Non-oxidative phase 2.3 Regulation 3 See also 4 Erythrocytes and the pentose phosphate pathway 5 References 6 External links
Outcome
The primary results of the Pathway are:
The generation of reducing equivalents, in the form of NADPH, used in reductive biosynthesis reactions within cells. (e.g. fatty acid synthesis) Production of ribose-5-phosphate (R5P), used in the synthesis of nucleotides and nucleic acids. Production of erythrose-4-phosphate (E4P), used in the synthesis of aromatic amino acids.
Aromatic amino acids, in turn, are precursors for many biosynthetic pathways, notably including the lignin in wood. 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, and is found to be most active in the liver, mammary gland and adrenal cortex in the human. However, the pathway is absent in skeletal muscle tissue. 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. One of the uses of NADPH in the cell is to prevent oxidative stress. It reduces glutathione via glutathione reductase, which converts reactive H2O 2 into H2O by glutathione peroxidase. If absent, the H2O2 would be converted to hydroxyl free radicals by Fenton chemistry, which can attack the cell. In a significant step, erythrocytes generate, through the pentose phosphate pathway, a large amount of NADPH used in the reduction of glutathione. Hydrogen peroxide is also generated for phagocytes in a process often referred to as a respiratory burst.[2]
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), 6phosphoglucono--lactone (2), 6-phosphogluconate (3), ribulose 5-phosphate (4).
The entire set of reactions can be summarized as follows: Reactants Glucose 6phosphate + NADP+ Products Enzyme Description Dehydrogenation. The hemiacetal hydroxyl group located on carbon 1 of glucose 6phosphate is converted into a carbonyl group, generating a lactone, and, in the process, NADPH is generated.
-lactone + H2O + H+ 6 ribulose 56-phosphogluconate phosphogluconate phosphate + dehydrogenase NADPH + CO2 + NADP+ The overall reaction for this process is:
Oxidative decarboxylation. NADP+ is the electron acceptor, generating another molecule of NADPH, a CO2, and ribulose 5phosphate.
Non-oxidative phase
Reactants ribulose 5-phosphate ribulose 5-phosphate xylulose 5-phosphate + ribose 5phosphate sedoheptulose 7-phosphate + glyceraldehyde 3-phosphate xylulose 5-phosphate + erythrose 4phosphate
Products ribose 5-phosphate xylulose 5-phosphate glyceraldehyde 3-phosphate + sedoheptulose 7-phosphate erythrose 4-phosphate + fructose 6phosphate
Regulation
Glucose-6-phosphate dehydrogenase is the rate-controlling enzyme of this pathway. It is allosterically stimulated by NADP+. The ratio of NADPH:NADP+ is normally about 100:1 in liver cytosol. This makes the cytosol a highlyreducing environment. An NADPH-utilizing pathway forms NADP+, which stimulates Glucose-6-phosphate dehydrogenase to produce more NADPH.
See also
G6PDH deficiency - A hereditary disease that disrupts the pentose phosphate pathway NADPH RNA thiamine deficiency
References
1. ^ Kruger NJ, von Schaewen A (June 2003). "The oxidative pentose phosphate pathway: structure and organisation" (http://linkinghub.elsevier.com/retrieve/pii/S1369526603000396) . Curr. Opin. Plant Biol. 6 (3): 236 46. doi:10.1016/S1369-5266(03)00039-6 (http://dx.doi.org/10.1016%2FS1369-5266%2803%2900039-6) . PMID 12753973 (http://www.ncbi.nlm.nih.gov/pubmed/12753973) . http://linkinghub.elsevier.com/retrieve/pii/S1369526603000396. 2. ^ Immunology at MCG 1/cytotox (http://www.lib.mcg.edu/edu/esimmuno/ch1/cytotox.htm) 3. ^ 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" (http://bloodjournal.hematologylibrary.org/cgi/content/full/92/7/2527) . Blood 92 (7): 252734. PMID 9746794 (http://www.ncbi.nlm.nih.gov/pubmed/9746794) . http://bloodjournal.hematologylibrary.org/cgi/content/full/92/7/2527.
External links
The chemical logic behind the pentose phosphate pathway (http://www2.ufp.pt/~pedros/bq/ppp.htm) MeSH Pentose+Phosphate+Pathway (http://www.nlm.nih.gov/cgi/mesh/2011/MB_cgi? mode=&term=Pentose+Phosphate+Pathway) Pentose phosphate pathway Map - Homo sapiens (http://www.genome.jp/dbget-bin/www_bget? path:hsa00030) Retrieved from "http://en.wikipedia.org/wiki/Pentose_phosphate_pathway" Categories: Metabolic pathways | Phosphorus This page was last modified on 30 August 2011 at 11:52. Text is available under the Creative Commons Attribution-ShareAlike License; additional terms may apply. See Terms of use for details. Wikipedia is a registered trademark of the Wikimedia Foundation, Inc., a non-profit organization.