4. (a) courses (such as this one) that NADH produced through glycoly- H °H sis in the cytosol can be used to generate ATP in the mitochon- dria. Yet, if 7-(14C)-NADH (in which the nicotinamide C-7 position is radioactively labeled; see diagram on the right) is added to rat hepatocytes, no radioactivity appears in the mitochondrial matrix while, if 4-(H)-NADH is added to hepatocytes, the tritium label soon appears in the mitochondrial matrix. Explain. It is generally stated and taught in biochemistry н, NH2 NH2 R R [4-°H]NADH [7-14CINADH

4. (a) courses (such as this one) that NADH produced through glycoly- H °H sis in the cytosol can be used to generate ATP in the mitochon- dria. Yet, if 7-(14C)-NADH (in which the nicotinamide C-7 position is radioactively labeled; see diagram on the right) is added to rat hepatocytes, no radioactivity appears in the mitochondrial matrix while, if 4-(H)-NADH is added to hepatocytes, the tritium label soon appears in the mitochondrial matrix. Explain. It is generally stated and taught in biochemistry н, NH2 NH2 R R [4-°H]NADH [7-14CINADH

Biology: The Dynamic Science (MindTap Course List)

4th Edition

ISBN:9781305389892

Author:Peter J. Russell, Paul E. Hertz, Beverly McMillan

Publisher:Peter J. Russell, Paul E. Hertz, Beverly McMillan

Chapter7: Cellular Respiration: Harvesting Chemical Energy

Section: Chapter Questions

Problem 7TYK

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1 a) What is meant by the ATP currency exchange ratio? Why does the oxidation of mitochondrial FADH2 generate one less ATP than oxidation of mitochondrial NADH? b) If 12 H+ are moved across the inner mitochondrial membrane by NADH oxidation, and each ATP synthesized requires 3 H+ to move through ATP synthase, why are only 3 ATP molecules produced by oxidation of each NADH?
When the cells of our body are in dire need to synthesize Ribose 5 phosphate and it has already enough supply of NADPH, reverse non oxidative pathway of the HMP shunt pathway takes place. If the cell has 10 glucose 6 phosphate molecules, how many of these would be converted to Fructose 6 phosphate and how many to form glyceraldehyde 3 phosphate respectively to synthesize maximum number of Ribose 5 phosphate? 8:2 2:8 4:6 6:4
1. What molecule are released in the formation of alpha- ketoglutarate into succinyl CoA? A. fad - fadh + h20 B. Fad- fadh C. Nadh+ co2 D. Acetl coa + co2 2.fad is reduced in which of the reaction of the krebs cycle? 3. How many nadh and fadh2 molecules are prodcues respectively during one turn of the citric acid cycle? 4. Acetyl coa is formed from pyruvate by ___ reaction. 5. What enzyme un the ETC is responsibke for generating the atp molecules?
7. Why are electron carriers (NAD+/NADH and FAD/FADH2) so important in the process of cellular respiration? a) They deliver electrons to the ETC, which in turn sets up chemiosmosis, where most of the ATP is generated. b) They separate the electrons from the protons so that the protons can be moved out of the mitochondrion. c) NADH and FADH2 are major components of the ETC, so without them, there would be no ETC in the cell. d) The electrons that they carry are able to directly phosphorylate ADP in order to generate the bulk of ATP in the cell. e) They transport protons across the mitochondrial membrane.
Consider the typical beta oxidation of linoleic acid (C18:2 ^Δ9, 12): How many ATP are generated in complete oxidation of linoleic acid? How many NADH are generated in complete oxidation of linoleic acid? How many FADH2 are generated in complete oxidation of linoleic acid?
1. Identify the oxidized coenzyme (letter abbreviation only) that participates in this reaction of the Kreb’s cycle. Succinate --> Fumarate 2. How many mol of NADH can be obtained upon the beta oxidation of stearic acid? 3. How many mol of ATP can be obtained upon the complete oxidation of 1 mol stearic acid? 4. How many steps in glycolysis in which ATO is converted to ADP?
5. a) The cell creates molecules of NADH and FADH2to use in the electron transport chain as they are electron carrier molecules. The electron transfers from these moleculesdrives the movement of what molecule across the mitochondrial membrane?b) What is chemiosmosis?c) How does the cell use chemiosmosis to drive overcome the thermodynamic barrier of bringing phosphates close togehter to create ATP?d) What steps of oxidative phosphorylation are in the cytosol and which are in the mitochondria?e) Cellular respiration can be controlled at the post-translational level. What does this mean, using GLUT as an example? Why is post-translational control of GLUT evolutionarilyadaptive over transcriptional control?f) How does establishment of equillibria of various molecules control metabolic reactions? What are three ways high ATP in the cell control cellular respiration?g) Why are the enzymes controlling the initial steps of various biochemical pathways are targeted by allosteric control?
Which step(s) of cellular respiration would be directly inhibited by high concentrations of NADH? How would this affect other steps of cellular respiration?
Which of the following statements about the malate-aspartate shuttle is false? a) 2.5 ATPs are formed per cytoplasmic NADH shuttled. b) Transamination is involved. c) Cytoplasmic oxaloacetate is converted to malate. d) Mitochondrial malate is converted to oxaloacetate. e) Antiport transport is not involved.
1) When a de-coupler such as 2,4-DNP is added to a respiring mitochondrion, which of the following effects on the process of ETC-OP will be true, which will be false. a) Mitochondria no longer reduce O2 to H2 b) Electrons no longer enter the electron transport chain. c) Activity of Complex V (ATP Synthase) is greatly decreased. d) The P/O ratio for FADH2 becomes larger than the P/O ratio for NADH. e) Protons are no longer pumped from the mitochondrial matrix to the intermembrane space. 2) The rate-limiting step in fatty acid synthesis is: a) condensation of acetyl-CoA and malonyl-CoA. b) formation of acetyl-CoA from acetate. c) formation of malonyl-CoA from malonate and coenzyme A. d) the reaction catalyzed by acetyl-CoA carboxylase.
The inhibitor X prevents coenzyme Q (Q) from participating in electron transfer in the electrontransport chain.(a) Will the presence of X prevent electrons from N ADH from passing through the electron trans-port chain? Explain why or why not.(b) Compound Y is a non-physiological reducing agent capable of directly reducing cytochromec1 in Complex III. Would oxygen consumption resume upon the addition of compound Y tomitochondria inhibited by inhibitor X? Be sure to explain your answer.
1. How many NADH _____& ATP _____are produced from the beta oxidation of Lauric Acid? 2. How many FADH2 _____& ATP _____are produced from the beta oxidation of Lauric Acid?