A report on Mitochondrion and Flavin adenine dinucleotide

Two mitochondria from mammalian lung tissue displaying their matrix and membranes as shown by electron microscopy
Reaction of FAD to form FADH2
Simplified structure of a mitochondrion.
Approximate absorption spectrum for FAD
Cross-sectional image of cristae in a rat liver mitochondrion to demonstrate the likely 3D structure and relationship to the inner membrane
Mechanism 1. Hydride transfer occurs by addition of H+ and 2 e−
Electron transport chain in the mitochondrial intermembrane space
Mechanism 2. Hydride transfer by abstraction of hydride from NADH
Transmission electron micrograph of a chondrocyte, stained for calcium, showing its nucleus (N) and mitochondria (M).
Mechanism 3. Radical formation by electron abstraction
Typical mitochondrial network (green) in two human cells (HeLa cells)
Mechanism 4. The loss of hydride to electron deficient R group
Model of the yeast multimeric tethering complex, ERMES
Mechanism 5. Use of nucleophilic addition to break R1-R2 bond
Evolution of MROs
Mechanism 6. Carbon radical reacts with O2 and acid to form H2O2
The circular 16,569 bp human mitochondrial genome encoding 37 genes, i.e., 28 on the H-strand and 9 on the L-strand.
Riboflavin
FADH{{sub|2}}

Flavoproteins are mainly located in the mitochondria because of their redox power.

- Flavin adenine dinucleotide

The citric acid cycle oxidizes the acetyl-CoA to carbon dioxide, and, in the process, produces reduced cofactors (three molecules of NADH and one molecule of FADH2) that are a source of electrons for the electron transport chain, and a molecule of GTP (which is readily converted to an ATP).

- Mitochondrion
Two mitochondria from mammalian lung tissue displaying their matrix and membranes as shown by electron microscopy

8 related topics with Alpha

Overall
Overview of the citric acid cycle

Citric acid cycle

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Series of chemical reactions to release stored energy through the oxidation of acetyl-CoA derived from carbohydrates, fats, and proteins.

Series of chemical reactions to release stored energy through the oxidation of acetyl-CoA derived from carbohydrates, fats, and proteins.

Overview of the citric acid cycle
Structural diagram of acetyl-CoA: The portion in blue, on the left, is the acetyl group; the portion in black is coenzyme A.

In eukaryotic cells, the citric acid cycle occurs in the matrix of the mitochondrion.

The overall yield of energy-containing compounds from the citric acid cycle is three NADH, one FADH2, and one GTP.

Interactive animation of the structure of ATP

Adenosine triphosphate

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Organic compound and hydrotrope that provides energy to drive many processes in living cells, such as muscle contraction, nerve impulse propagation, condensate dissolution, and chemical synthesis.

Organic compound and hydrotrope that provides energy to drive many processes in living cells, such as muscle contraction, nerve impulse propagation, condensate dissolution, and chemical synthesis.

Interactive animation of the structure of ATP
The cycles of synthesis and degradation of ATP; 2 and 1 represent input and output of energy, respectively.
This image shows a 360-degree rotation of a single, gas-phase magnesium-ATP chelate with a charge of −2. The anion was optimized at the UB3LYP/6-311++G(d,p) theoretical level and the atomic connectivity modified by the human optimizer to reflect the probable electronic structure.
An example of the Rossmann fold, a structural domain of a decarboxylase enzyme from the bacterium Staphylococcus epidermidis with a bound flavin mononucleotide cofactor.

ATP production by a non-photosynthetic aerobic eukaryote occurs mainly in the mitochondria, which comprise nearly 25% of the volume of a typical cell.

NADH and FADH2 are recycled (to NAD+ and FAD, respectively) by oxidative phosphorylation, generating additional ATP.

The electron transport chain in the mitochondrion is the site of oxidative phosphorylation in eukaryotes. The NADH and succinate generated in the citric acid cycle are oxidized, which releases the energy of oxygen to power ATP synthase.

Electron transport chain

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Series of protein complexes and other molecules that transfer electrons from electron donors to electron acceptors via redox reactions (both reduction and oxidation occurring simultaneously) and couples this electron transfer with the transfer of protons (H+ ions) across a membrane.

Series of protein complexes and other molecules that transfer electrons from electron donors to electron acceptors via redox reactions (both reduction and oxidation occurring simultaneously) and couples this electron transfer with the transfer of protons (H+ ions) across a membrane.

The electron transport chain in the mitochondrion is the site of oxidative phosphorylation in eukaryotes. The NADH and succinate generated in the citric acid cycle are oxidized, which releases the energy of oxygen to power ATP synthase.
Photosynthetic electron transport chain of the thylakoid membrane.
Depiction of ATP synthase, the site of oxidative phosphorylation to generate ATP.

The energy released by reactions of oxygen and reduced compounds such as cytochrome c and (indirectly) NADH and FADH is used by the electron transport chain to pump protons into the intermembrane space, generating the electrochemical gradient over the inner mitochondrial membrane.

Most eukaryotic cells have mitochondria, which produce ATP from reactions of oxygen with products of the citric acid cycle, fatty acid metabolism, and amino acid metabolism.

Typical eukaryotic cell

Cellular respiration

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Set of metabolic reactions and processes that take place in the cells of organisms to convert chemical energy from nutrients into adenosine triphosphate , and then release waste products.

Set of metabolic reactions and processes that take place in the cells of organisms to convert chemical energy from nutrients into adenosine triphosphate , and then release waste products.

Typical eukaryotic cell
Out of the cytoplasm it goes into the Krebs cycle with the acetyl CoA. It then mixes with CO2 and makes 2 ATP, NADH, and FADH. From there the NADH and FADH go into the NADH reductase, which produces the enzyme. The NADH pulls the enzyme's electrons to send through the electron transport chain. The electron transport chain pulls H+ ions through the chain. From the electron transport chain, the released hydrogen ions make ADP for an result of 32 ATP. O2 provides most of the energy for the process and combines with protons and the electrons to make water. Lastly, ATP leaves through the ATP channel and out of the mitochondria.
Stoichiometry of aerobic respiration and most known fermentation types in eucaryotic cell. Numbers in circles indicate counts of carbon atoms in molecules, C6 is glucose C6H12O6, C1 carbon dioxide CO2. Mitochondrial outer membrane is omitted.

Although carbohydrates, fats, and proteins are consumed as reactants, aerobic respiration is the preferred method of pyruvate breakdown in glycolysis, and requires pyruvate to the mitochondria in order to be fully oxidized by the citric acid cycle.

The products of this process are carbon dioxide and water, and the energy transferred is used to break bonds in ADP to add a third phosphate group to form ATP (adenosine triphosphate), by substrate-level phosphorylation, NADH and FADH2

The electron transport chain in the cell is the site of oxidative phosphorylation. The NADH and succinate generated in the citric acid cycle are oxidized, releasing the energy of O2 to power the ATP synthase.

Oxidative phosphorylation

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Metabolic pathway in which cells use enzymes to oxidize nutrients, thereby releasing chemical energy in order to produce adenosine triphosphate (ATP).

Metabolic pathway in which cells use enzymes to oxidize nutrients, thereby releasing chemical energy in order to produce adenosine triphosphate (ATP).

The electron transport chain in the cell is the site of oxidative phosphorylation. The NADH and succinate generated in the citric acid cycle are oxidized, releasing the energy of O2 to power the ATP synthase.
Reduction of coenzyme Q from its ubiquinone form (Q) to the reduced ubiquinol form (QH2).
Complex I or NADH-Q oxidoreductase. The abbreviations are discussed in the text. In all diagrams of respiratory complexes in this article, the matrix is at the bottom, with the intermembrane space above.
Complex II: Succinate-Q oxidoreductase.
The two electron transfer steps in complex III: Q-cytochrome c oxidoreductase. After each step, Q (in the upper part of the figure) leaves the enzyme.
Complex IV: cytochrome c oxidase.
Mechanism of ATP synthase. ATP is shown in red, ADP and phosphate in pink and the rotating γ subunit in black.

In eukaryotes, this takes place inside mitochondria.

The energy stored in the chemical bonds of glucose is released by the cell in the citric acid cycle producing carbon dioxide, and the energetic electron donors NADH and FADH.

Solution NMR structure of protein NMA1147 from Neisseria meningitidis. Northeast structural genomics consortium target mr19

Succinate dehydrogenase

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Enzyme complex, found in many bacterial cells and in the inner mitochondrial membrane of eukaryotes.

Enzyme complex, found in many bacterial cells and in the inner mitochondrial membrane of eukaryotes.

Solution NMR structure of protein NMA1147 from Neisseria meningitidis. Northeast structural genomics consortium target mr19
Image 5: Subunits of succinate dehydrogenase
Image 6: E2 Succinate oxidation mechanism.
Image 7: E1cb Succinate oxidation mechanism.
Image 8: Ubiquinone reduction mechanism.
Image 9: Electron carriers of the SQR complex. FADH2, iron-sulfur centers, heme b, and ubiquinone.

Mitochondrial and many bacterial SQRs are composed of four structurally different subunits: two hydrophilic and two hydrophobic.

SdhA contains a covalently attached flavin adenine dinucleotide (FAD) cofactor and the succinate binding site and SdhB contains three iron-sulfur clusters: [2Fe-2S], [4Fe-4S], and [3Fe-4S].

Schematic demonstrating mitochondrial fatty acid beta-oxidation and effects of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency, LCHAD deficiency

Beta oxidation

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Schematic demonstrating mitochondrial fatty acid beta-oxidation and effects of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency, LCHAD deficiency
Complete beta oxidation of linoleic acid (an unsaturated fatty acid).

In biochemistry and metabolism, beta-oxidation is the catabolic process by which fatty acid molecules are broken down in the cytosol in prokaryotes and in the mitochondria in eukaryotes to generate acetyl-CoA, which enters the citric acid cycle, and NADH and FADH2, which are co-enzymes used in the electron transport chain.

Ribbon diagram of a monomer of human MAO-A, with FAD and clorgiline bound, oriented as if attached to the outer membrane of a mitochondrion. From.

Monoamine oxidase

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Monoamine oxidases (MAO) are a family of enzymes that catalyze the oxidation of monoamines, employing oxygen to clip off their amine group.

Monoamine oxidases (MAO) are a family of enzymes that catalyze the oxidation of monoamines, employing oxygen to clip off their amine group.

Ribbon diagram of a monomer of human MAO-A, with FAD and clorgiline bound, oriented as if attached to the outer membrane of a mitochondrion. From.
Norepinephrine degradation. Monoamine oxidase is shown left in the blue box.
Ribbon diagram of human MAO-B. From.

They are found bound to the outer membrane of mitochondria in most cell types of the body.

Monoamine oxidases contain the covalently bound cofactor FAD and are, thus, classified as flavoproteins.