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Carbohydrate
Metabolism
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Glycolysis
Pathway Glycolysis was one of the first metabolic pathways studied and is one of the best understood, in terms of the enzymes involved, their mechanisms of action, and the regulation of the pathway to meet the needs of the organism and the cell. The glycolytic pathway is extremely ancient in evolution, and is common to essentially all living organisms. |
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Lactose
Synthesis
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Oxidative reactions of the pentose phosphate pathway
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Starch Synthesis
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Sucrose Synthesis
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The Citric Acid Cycle
The Krebs cycle, also called the citric acid cycle, is a fundamental metabolic pathway involving eight enzymes essential for energy production through aerobic respiration, and, like glycolysis, arose early in evolution. This pathway is also an important source of biosynthetic building blocks used in gluconeogenesis, amino acid biosynthesis, and fatty acid biosynthesis. |
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Fatty
Acids and Lipid Metabolism
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Beta-Oxidation of Fatty Acids
Fatty acids provide highly efficient energy storage, storing much more energy for their weight than carbohydrates like glucose. Fatty acids are stored as triglycerides in adipose tissue, in which each triglyceride molecule contains three fatty acids and one glycerol. |
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Formation of Ketone Bodies from
acetyl-CoA
The acetyl-CoA produced by mitochondrial beta-oxidation of fatty acids enters the Kreb's cycle to produce energy, but that is not the only fate of
acetyl-CoA. In liver mitochondria, some
acetyl-CoA is converted to acetoacetate, beta-hydroxybutyrate, and acetone, collectively called ketone bodies. |
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Mitochondrial Carnitine Palmitoyltransferase
(CPT) System
The oxidation of fatty acids is an important source of energy for ATP production in mitochondria through the entry of
acetyl-CoA into the Krebs cycle. Fatty acids are oxidized inside the mitochondrial matrix but the fatty acids to be oxidized come from the
cytos |
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Omega Oxidation
While the main route of fatty acid metabolism is through beta-oxidation, some minor metabolic pathways such as omega oxidation also contribute to the metabolism of fatty acids and other molecules. Omega oxidation occurs in the endoplasmic reticulum rather than the mitochondria, the site of beta-oxidation. |
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Oxidation
of odd-numbered chain fatty acid, from
Propionyl-CoA to Succinyl-CoA
The beta-oxidation of fatty acids in
mitochondria progressively shortens fatty
acids two-carbons at a time as acetyl-CoA
units are removed with each round of the
cycle. Fatty acids that enter beta-oxidation
with an even number of carbons are converted
entirely to acetyl-CoA, with the last round
producing two acetyl-CoA molecules from one
four carbon fatty acid. |
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Oxidation
of Polyunsaturated Fatty Acid Unsaturated fatty acids are those that contain one or more double bonds in their alkyl-chain. Polyunsaturated fats with two double bonds usually have one between carbons 9 and 10 in the alkyl chain and another three carbons away (carbons 12-13).
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Amino
Acid Metabolism
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Biosynthesis of
Arginine in Bacteria |
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Biosynthesis of Chorismate in Bacteria and Plants
The biosynthesis of all three aromatic amino acids (tryptophan, tyrosine and phenylalanine) begins with the metabolic intermediate chorismate.
The biosynthesis of chorismate occurs only in plants and bacterial, not in animals. The first step in the pathway involves phosphoenolpyruvate (PEP) from glycolysis and erythrose-4-phosphate from the pentose phosphate pathway. |
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Biosynthesis of isoleucine
Isoleucine is an essential amino acid, only synthesized in plants and bacteria, and required in the diet by animals. In proteins, the hydrophobic isoleucine side-chain tends to reside with other hydrophobic residues in the interior of globular proteins or in transmembrane domains. Isoleucine biosynthesis begins with the common metabolic intermediate pyruvate, the endpoint of glycolysis.
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Biosynthesis of leucine
The Krebs cycle, also called the citric acid cycle, is a fundamental metabolic pathway involving eight enzymes essential for energy production through aerobic respiration, and, like
glycolysis, arose early in evolution. This pathway is also an important source of biosynthetic building blocks used in
gluconeogenesis, amino acid biosynthesis, and fatty acid biosynthesis. |
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Biosynthesis of
Lysine in Bacteria
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Biosynthesis of neurotransmitters
Neurotransmitters are signaling
molecules used by neurons to communicate
across chemical synapses. The receptors for
neurotransmitters include G-protein coupled
receptors (GPCRs) and ligand-gated ion
channels. |
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Biosynthesis of phenylalanine and tyrosine in bacteria and plants
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Biosynthesis of Proline in Bacteria
Among the twenty amino acids encoded by the genetic code, proline is unique in having a cyclic structure with its side chain connected to the amino group to create a secondary amine. As a consequence of its cyclic structure, proline constrains the structure of proteins where it occurs, disrupting alpha-helices. |
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Biosynthesis of spermidine and spermine
The polyamines spermidine and spermine are expressed in a variety of tissues and are involved in the regulation of apoptosis, cellular proliferation, and progression through the cell cycle. Depletion of polyamines appears to reduce cell growth, and increased polyamine expression is associated with the cancer development and progression, making polyamine biosynthesis a target for the control of cancer. |
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Biosynthesis of threonine and methionine |
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Biosynthesis of Tryptophan in Bacteria and Plants
The aromatic amino acid tryptophan is an essential nutrient, meaning that humans and animals do not themselves have the biosynthetic machinery to synthesize tryptophan but rely on dietary intake from bacteria and plants that do produce it. |
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Biosynthesis
of valine |
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Catabolic
pathways for alanine, glycine, serine,
cysteine, tryptophan, and threonine Amino acids in the diet have one of two fates - either they are incorporated into proteins or they are broken down for energy and metabolic intermediates. They are not stored and the body also does not excrete them intact.
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Catabolic
Pathways for Arginine, Histidine, Glutamate,
Glutamine and Proline
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Catabolic
Pathway for Asparagine and Asparate |
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Catabolic
Pathway for Methionine, Isoleucine, Threonine
and Valine |
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Serine in E. Coli Pathway
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The reactions that feed amino groups into the urea cycle
Excess amino acids in the body can be used as a source of energy, with their carbon skeleton converted to metabolic intermediates such as acetyl-CoA or intermediates in the Krebs cycle.
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Nucleotide
Metabolism
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Coming Soon
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Energy
Metabolism
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Electrons -Transfer Reaction in Mitochondria |
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