Pentose phosphate pathway

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Pentose phosphate pathway

HMBP

HMBP

Glycolysis
Citric acid cycle
Electron transport chain and oxidative phosphorylation
Gluconeogenesis
Glycogen metabolism
Pentose phosphate pathway
Physiological changes during exercise
Amino acid metabolism
Nitrogen and urea cycle
Fatty acid synthesis
Fatty acid oxidation
Ketone body metabolism
Cholesterol metabolism
Essential fructosuria
Hereditary fructose intolerance
Galactosemia
Pyruvate dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Lactose intolerance
Glycogen storage disease type I
Glycogen storage disease type II (NORD)
Glycogen storage disease type III
Glycogen storage disease type IV
Glycogen storage disease type V
Leukodystrophy
Metachromatic leukodystrophy (NORD)
Krabbe disease
Gaucher disease (NORD)
Niemann-Pick disease types A and B (NORD)
Niemann-Pick disease type C
Fabry disease (NORD)
Tay-Sachs disease (NORD)
Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD)
Mucopolysaccharide storage disease type 2 (Hunter syndrome) (NORD)
Cystinosis
Hartnup disease
Alkaptonuria
Ornithine transcarbamylase deficiency
Phenylketonuria (NORD)
Cystinuria (NORD)
Homocystinuria
Maple syrup urine disease
Abetalipoproteinemia
Familial hypercholesterolemia
Hypertriglyceridemia
Hyperlipidemia
Disorders of carbohydrate metabolism: Pathology review
Disorders of fatty acid metabolism: Pathology review
Dyslipidemias: Pathology review
Glycogen storage disorders: Pathology review
Lysosomal storage disorders: Pathology review
Disorders of amino acid metabolism: Pathology review
Cellular structure and function
Cell membrane
Selective permeability of the cell membrane
Extracellular matrix
Cell-cell junctions
Endocytosis and exocytosis
Osmosis
Resting membrane potential
Nernst equation
Cytoskeleton and intracellular motility
Cell signaling pathways
Adrenoleukodystrophy (NORD)
Zellweger spectrum disorders (NORD)
Primary ciliary dyskinesia
Alport syndrome
Ehlers-Danlos syndrome
Osteogenesis imperfecta
Marfan syndrome
Vitamin C deficiency
Peroxisomal disorders: Pathology review
Nuclear structure
DNA structure
Transcription of DNA
Translation of mRNA
Gene regulation
Epigenetics
Amino acids and protein folding
Protein structure and synthesis
Nucleotide metabolism
DNA replication
Lac operon
DNA damage and repair
Cell cycle
Mitosis and meiosis
DNA mutations
Lesch-Nyhan syndrome
Orotic aciduria
Adenosine deaminase deficiency
Xeroderma pigmentosum
Li-Fraumeni syndrome
Bloom syndrome
Fanconi anemia
McCune-Albright syndrome
Acute radiation syndrome
Purine and pyrimidine synthesis and metabolism disorders: Pathology review
Polymerase chain reaction (PCR) and reverse-transcriptase PCR (RT-PCR)
Gel electrophoresis and genetic testing
ELISA (Enzyme-linked immunosorbent assay)
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DNA cloning
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Independent assortment of genes and linkage
Evolution and natural selection
Down syndrome (Trisomy 21)
Edwards syndrome (Trisomy 18)
Patau syndrome (Trisomy 13)
Fragile X syndrome
Huntington disease
Myotonic dystrophy
Friedreich ataxia
Turner syndrome
Klinefelter syndrome
Prader-Willi syndrome
Angelman syndrome
Beckwith-Wiedemann syndrome
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Williams syndrome
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Tuberous sclerosis
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Autosomal trisomies: Pathology review
Muscular dystrophies and mitochondrial myopathies: Pathology review
Miscellaneous genetic disorders: Pathology review

Transcript

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Content Reviewers

Let’s say you just ate a carbohydrate loaded meal, like a bowl of rice.

A few hours after you’re done, those carbohydrates are broken down in the small intestine into their simplest chemical form; monosaccharides, the most important of which is glucose - a 6-carbon molecule that’s in the shape of a ring.

Glucose moves from the small intestine into the bloodstream, and blood glucose levels rise, which causes the pancreas to secretes a hormone called insulin.

Insulin makes more glucose enter cells through specific transporters called GLUTs.

Once glucose is in the cell, an enzyme called hexokinase attaches a phosphate group to its sixth carbon, creating glucose-6-phosphate.

From there, the cell has the option to take glucose through a metabolic pathway called glycolysis; which is the breakdown of glucose in order to generate ATP.

But if the cell doesn’t need ATP, glucose can be used to make some other useful products by entering an alternative metabolic pathway called the pentose phosphate pathway.

The pentose phosphate pathway is named for the products it ultimately generates; pentose refers to a five-carbon sugar called ribose, and phosphate refers to a molecule called nicotinamide adenine dinucleotide phosphate, or NADPH.

So the pentose phosphate pathway is an alternative pathway that glucose can enter when cells need to make more ribose and NADPH.

Ribose can be used to make nucleotides, which are the building blocks of our DNA and RNA.

And NADPH is rich in electrons, and can be used in various anabolic pathways.

Anabolic pathways are ones that synthesize molecules like fatty acids, from scratch, and require an electron donor - such as NADPH.

Like glycolysis, the pentose phosphate pathway happens exclusively in the cytoplasm and it doesn’t require any special organelles which means that all of our cells can use this pathway.

The pentose phosphate pathway can be divided into two phases: an irreversible oxidative phase that ultimately yields NADPH, and a reversible non-oxidative phase that yields ribose.

Irreversible means that the reaction can only go in one direction - that is, substrate to product.

On the other hand, reversible means that the reaction can go in both directions, and the substrate and product can be interconverted into one another, depending on what the body needs more.

Oxidation of a molecule means that a molecule donates or loses its electrons - in the form of hydrogens - to another molecule.

Okay, to launch the oxidative phase, an enzyme called glucose-6-phosphate dehydrogenase, or G6PD, snatches a hydrogen from glucose-6-phosphate, and offers it to NADP+, making 6-phosphogluconate and NADPH in the process.

This is the rate-limiting step of the pentose phosphate pathway.

The rate-limiting step of any reaction is the step that takes the longest to happen, so it determines the overall rate of the pathway.

The next step involves an enzyme called 6-phosphogluconate dehydrogenase, which, much like G6PD, steals an electron from 6-phosphogluconate and offers it to another NADP+, making our second NADPH.

But unlike G6PD, this enzyme also removes a carbon from the 6-carbon 6-phosphogluconate and releases it as carbon dioxide, making a 5-carbon sugar called ribulose-5-phosphate.

This marks the end of the oxidative phase, with a total of 2 NADPH molecules created per glucose.

Now, since NADPH is electron-rich, it’s time for it to give back to the cellular community.

NADPH can donate electrons in anabolic pathways such as fatty acid synthesis, steroid hormone synthesis, and cholesterol synthesis.

So there’s usually a lot of NADPH in tissues that make these molecules, like the liver, the adrenal cortex, the gonads, and the milk-producing breast glands.

In addition to anabolic pathways, NADPH is also a key player for antioxidant reactions.

For example, red blood cells normally produce reactive oxygen species such as hydrogen peroxide as a byproduct of oxygen metabolism.