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Derived copy of Bis2A 07.3 Oxidation of Pyruvate and the Citric Acid
Derived copy of Bis2A 07.3 Oxidation of Pyruvate and the Citric Acid

... † http://cnx.org/content/m56028/1.2/ ‡ http://creativecommons.org/licenses/by/4.0/ ...
Generation of Biochemical Energy
Generation of Biochemical Energy

... The eight steps of the cycle produce two molecules of carbon dioxide, four molecules of reduced coenzymes, and one energy-rich phosphate (GTP). The final step regenerates the reactant for step 1 of the next turn of the cycle. ...
anaerobic and aerobic respiration
anaerobic and aerobic respiration

... Some prokaryotes are able to carry out anaerobic respiration, respiration in which an inorganic molecule other than oxygen (O2) is the final electron acceptor. For example, some bacteria called soleplate reducers can transfer electrons to soleplate (SO42-) reducing it to H2S. Other bacteria, called ...
8 - student.ahc.umn.edu
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... coenzyme Q donate four electrons. Two of those electrons produce two molecules of reduced cytochrome c and the other two electrons end up regenerating a molecule of QH2. Slide 18. Cytochrome c oxidase. If you thought that the last reaction sequence was complicated, here is something even more baroqu ...
chapter 11 - rci.rutgers.edu
chapter 11 - rci.rutgers.edu

... CHAPTER 17 ...
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... NAD  NADH (Reduced/Oxidized)  Carried to ETC : at Glycolysis, Krebs cycle NADH  NAD (Reduced/Oxidized) : at ETC ( Electron Transport Chain ) *The more reduced = the more energy it holds. ...
PHARMACY BIOMEDICAL PREVIEW PROGRAM 2014
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... • Also known as the Tricarboxylic Acid (TCA) Cycle and the Kreb’s Cycle. ...
BI 200 - Exam #2
BI 200 - Exam #2

... 23. In eukaryotic mitochondria enzymes of the Krebs cycle are found in the _________ and components of the electron transport chain are associated with the ____________. a. cristae; matrix b. cytoplasm; cristae c. matrix; cristae d. none of the above – eukaryotes don’t have mitochondria 24. In chem ...
CITRIC ACID (KREB`S, TCA) CYCLE
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... Acetyl CoA, citrate, and succinylCoA are the end products of individual steps in the citric acid cycle and their accumulation inhibits the step involved in their production. That, of course, results in inhibition of the cycle as a whole. Finally, Ca++ stimulates the citric acid cycle at several poin ...
Bis2A 07.3 Oxidation of Pyruvate and the Citric
Bis2A 07.3 Oxidation of Pyruvate and the Citric

... † http://cnx.org/content/m44433/1.7/ ‡ http://creativecommons.org/licenses/by/4.0/ ...
Cellular respiration - Lake City Public Schools High School
Cellular respiration - Lake City Public Schools High School

... CoA combines with a four-carbon molecule to form a six-carbon citrate molecule. In a series of events, the citrate reforms a four-carbon molecule. With each turn of the cycle, one ATP and two carbon dioxide molecules are released. NADH and FADH2 are also produced. The cycle must turn twice to proces ...
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... • Know overall reaction equation, including how many ATP, NADH, and pyruvate are formed. • Given the structure of each intermediate in the pathway, explain what is happening chemically in each step, the type of reaction(s), and the type of enzyme that catalyzes the reaction. 11. Explain the th ...
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... subunits (α3 : β3 : γ : δ : ε : a : b2 : cx) and the eukaryotic V-ATPase has thirteen subunits (A3 : B3 : C : D : E : F : G2 : Hx : a : d : cx : c’x : c’’x).2 The A-ATP synthase is composed of two functional sectors; a water soluble A1 part, containing the catalytic sites, and the membrane bound AO ...
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... changes shape so its active site embraces the substrates (induced fit). ...
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... • a. Electron transport and oxygen consumption are inhibited • b. Electron transport and phosphorylation of ADP remain tightly coupled • c. The inner mitochondrial membrane remains impermeable to protons • d. Protons pass through the membrane-bound Fo fragment, but they do not sustain any ATP format ...
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... slopes of the primary double-reciprocal plots (of reaction rate against ATP concentration) as a function of inhibitor concentration were linear. When pyruvate was the variable substrate, however, non-linear-slope replots were obtained. Non-linear-slope effects normally reflect multiple combination o ...
Fructose-1,6 - LSU School of Medicine
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... All the intermediates of glycolysis are part of gluconeogenesis In addition, gluconeogenesis involves oxaloacetate and (indirectly) malate O- ...
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biology 2402
biology 2402

... manageable amounts of energy from one molecule to another. ATP, the "energy currency" of a living cell, is the molecule that accomplishes this transfer of manageable energy. A typical cell has about a billion molecules of ATP, which usually lasts for less than a minuet before being used. It is there ...
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Journal of Biological Chemistry

... upon amino acid incorporation into protein of the liver ribosome system (Table II) just as effectively as it does the decrease in hepatic ATP concentration induced by the same analogue (3). These results tend to implicate cellular BTP deficiency as being important in the inhibition of protein synthe ...
Role of cryo-ET in membrane bioenergetics research
Role of cryo-ET in membrane bioenergetics research

... Upper panel: in mitochondria, ATP is generated by oxidative phosphorylation. Electrons are transferred from the electron donors NADH + and FADH + to O2 via NADH dehydrogenase (Complex I, blue), ubiquinone (UQ), cytochrome c reductase (Complex III, orange), cytochrome c (black), and cytochrome c oxid ...
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Adenosine triphosphate



Adenosine triphosphate (ATP) is a nucleoside triphosphate used in cells as a coenzyme often called the ""molecular unit of currency"" of intracellular energy transfer.ATP transports chemical energy within cells for metabolism. It is one of the end products of photophosphorylation, cellular respiration, and fermentation and used by enzymes and structural proteins in many cellular processes, including biosynthetic reactions, motility, and cell division. One molecule of ATP contains three phosphate groups, and it is produced by a wide variety of enzymes, including ATP synthase, from adenosine diphosphate (ADP) or adenosine monophosphate (AMP) and various phosphate group donors. Substrate-level phosphorylation, oxidative phosphorylation in cellular respiration, and photophosphorylation in photosynthesis are three major mechanisms of ATP biosynthesis.Metabolic processes that use ATP as an energy source convert it back into its precursors. ATP is therefore continuously recycled in organisms: the human body, which on average contains only 250 grams (8.8 oz) of ATP, turns over its own body weight equivalent in ATP each day.ATP is used as a substrate in signal transduction pathways by kinases that phosphorylate proteins and lipids. It is also used by adenylate cyclase, which uses ATP to produce the second messenger molecule cyclic AMP. The ratio between ATP and AMP is used as a way for a cell to sense how much energy is available and control the metabolic pathways that produce and consume ATP. Apart from its roles in signaling and energy metabolism, ATP is also incorporated into nucleic acids by polymerases in the process of transcription. ATP is the neurotransmitter believed to signal the sense of taste.The structure of this molecule consists of a purine base (adenine) attached by the 9' nitrogen atom to the 1' carbon atom of a pentose sugar (ribose). Three phosphate groups are attached at the 5' carbon atom of the pentose sugar. It is the addition and removal of these phosphate groups that inter-convert ATP, ADP and AMP. When ATP is used in DNA synthesis, the ribose sugar is first converted to deoxyribose by ribonucleotide reductase.ATP was discovered in 1929 by Karl Lohmann, and independently by Cyrus Fiske and Yellapragada Subbarow of Harvard Medical School, but its correct structure was not determined until some years later. It was proposed to be the intermediary molecule between energy-yielding and energy-requiring reactions in cells by Fritz Albert Lipmann in 1941. It was first artificially synthesized by Alexander Todd in 1948.
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