Pioglitazone, a drug used to treat diabetes, causes some membrane-embedded portions of mitochondrial Complex I to separate from the rest of the protein that includes the matrix “arm.” Predict the effect of pioglitazone on electron transport and ATP production. The protonmotive force is decreased, leading to less ATP produced by ATP synthase
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Pioglitazone, a drug used to treat diabetes, causes some membrane-embedded portions of mitochondrial Complex I to separate from the rest of the protein that includes the matrix “arm.” Predict the effect of pioglitazone on electron transport and ATP production.
The protonmotive force is decreased, leading to less ATP produced by ATP synthase.
The protonmotive force is increased, leading to more ATP produced by ATP synthase.
The protonmotive force is increased, leading to less ATP produced by ATP synthase.
The protonmotive force is decreased, leading to more ATP produced by ATP synthase.
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- Draw and label a lipid bilayer containing the large mitochondrial trans-membrane protein complexes representing complex I, II, III, and IV, and ATP Synthase. Make two more of these drawings. Label the first one mitochondrial electron source and using a different ink color, indicate the source(s) of electrons. Label the second mitochondrial energy source, and indicate the source of energy driving the electron transport chain. In the third, label the mitochondrial electron acceptor in its proper position. In this third drawing, also include ATP synthase (in its correct orientation-the spherical part is on the opposite side of the membrane as the H+ reservoir). Label your diagrams with the correct names for the membranes, ATP synthase, and to show where the protons (H+) are pumped to drive ATP synthesis.Draw and label a lipid bilayer containing the large mitochondrial trans-membrane protein complexes representing complex I, II, II, and IV, and ATP Synthase. Make two more of these drawings. Label the first one mitochondrial electron source and using a different ink color, indicate the source(s) of electrons. Label the second mitochondrial energy source, and indicate the source of energy driving the electron transport chain. In the third, label the mitochondrial electron acceptor in its proper position. In this third drawing, also include ATP synthase (in its correct orientation-the spherical part is on the opposite side of the membrane as the H+ reservoir). Label your diagrams with the correct names for the membranes, ATP synthase, and to show where the protons (H*) are pumped to drive ATP synthesis.Draw and label a lipid bilayer containing the large mitochondrial trans-membrane protein complexes representing complex I, II, III, and IV, and ATP Synthase. Label your diagrams with the correct names for the membranes, Make two more of these drawings. Label the first one mitochondrial electron source and using a different ink color, indicate the source(s) of electrons. Label the second mitochondrial energy source, and indicate the source of energy driving the electron transport chain. In the third, label the mitochondrial electron acceptor in its proper position. Also include ATP synthase (in its correct orientation-the spherical part is on the opposite side of the membrane as the H+ reservoir). Use a different color of ink to show where the protons (H+) are pumped to drive ATP synthesis. also indicate where ATP is generated and were the power is stored to generate ATP. NOW, do the same thing with chloroplasts. Draw and label a lipid bilayer containing the large photosynthetic…
- When the antibiotic X is added to actively respiring mitochondria, several things happen: the yield of ATP decreases, the rate of O2 consumption increases, heat is released, and the pH gradient across the inner mitochondrial membrane increases. Does X act as an uncoupler or an inhibitor of oxidative phosphorylation? Explain the experimental observations in terms of the antibiotic’s ability to transfer K+ ions across the inner mitochondrial membrane.Calcium is an important regulator of the citric acid cycle. Calcium is transported across the mitochondrial inner membrane by a Ca²- 2+ uniporter that is driven by the negative potential inside the matrix. Part A Assuming a membrane potential across the inner membrane of 172 mV (inside negative), calculate the ratio of the [Ca2+] in the matrix to that in the cytoplasm ([Ca2+]m/[Ca²+]c) that would exist at equilibrium (i.e., AG = 0). Express your answer using two significant figures. [Ca2+]m [Ca2+] = ΤΟ ΑΣΦ Submit Request Answer Part B ? Cytoplasmic [Ca2+] is on the order of 10-7 M in a healthy cell. Based on your answer in Part A, calculate the [Ca2+] that would exist in the matrix at equilibrium. Express your answer to two significant figures and include the appropriate units. ☐ μÅ ? Value UnitsThe four complexes of the electron transport chain use the energy of electrons stored in reducing agents to create a concentration gradient of protons (H*) across the mitochondrial inner membrane. Give the number of protons pumped into the intermembrane space by each of the four complexes: complex I: complex II: complex III: complex IV:
- The maintenance of a proton motive force across the inner mitochondrial membrane is crucial for continued ATP production. Surprisingly, it has been discovered that the inner membranes of certain cells contain proteins, called uncoupling proteins, that are capable of transporting protons from the intermembrane space to the mitochondrial matrix. Why would mitochondria contain transporters that essentially waste energy potential in the proton gradient?In the 1930s, some physicians prescribed low doses of a compound called dinitrophenol (DNP) to help patients lose weight. This unsafe method was abandoned after some patients died. DNP uncouples the chemiosmotic machinery by making the lipid bilayer of the inner mitochondrial membrane leaky to H+. Chemical agents that cause this effect are called uncouplers. Explain how this could cause weight loss and also death. Considering the danger, is there any use for compounds like DNP or other uncouplers?The majority of ATP production in aerobic cellular respiration occurs within the mitochondria during electron transport. In this phase of cellular respiration, NADH and FADH, are oxidized to become NAD+ and FAD+. The protons and electrons released during this axidation are used to establisha chemiosmotic gradient in the mitochondrial intermembrane space. The potential established by this gradient is used to convert mechanical energy into the chemical energy needed to join an inorganic phosphate on to ADP, thus creating ATP. Mitochondrial DNA Lamela er membrane Inner boundary membrane - Cristal membrane Matrin- Cristae Matrix granule Ribosome ATP synthase Intermembrane space Intracristal space Peripheral space Outer membrane Parins Mitochondrion structure by Kelvin13 (CC BY-SA 3.0) Outer membrane Cyt e ATP Synthase NADH NAD+H ATP Citric ADP acid cycle Matrix Suecinate Fumee Inner membrane Intermembrane space Mitochondrial electron transport chain by Fvasconcello (CCO) a. Analyze why…
- Electron transfer translocates protons from the mitochondrial matrix to the external medium, establishing a pH gradient across the inner membrane (outside more acidic than inside). The tendency of protons to diffuse back into the matrix is the driving force for ATP synthesis by ATP synthase. During oxidative phosphorylation by a suspension of mitochondria in a medium of pH 7.4,pH 7.4, the measured pH of the matrix is 7.7. Calculate [H+] in the external medium and in the matrix under these conditions. a)[H+]in the matrix: b)What is the outside‑to‑inside ratio of [H+]? c)What is the free‑energy change inherent in this concentration difference across the membrane? (Assume a temperature of 25 °C.25 °C.)A central tenet in mitochondrial bioenergetics is that exergonic electron transfer drives the creation of an electrical potential () across the inner mitochondrial membrane (IMM). This is entirely true. Another tenet of mitochondrial bioenergetics, that you will read everywhere, is that this electrical potential is created by three proton pumps, Complexes I, III and IV. This is less true. A proton pump is this: It’s a protein that binds a proton from one side of a membrane, translocates that very proton across the membrane, through the protein, and ejects it into solution on the other side of the membrane. Complex I is a proton pump, but we did not discuss complex I. Complex III is NOT a proton pump, yet it creates electrical potential across the IMM. It is an electron/proton charge separation device. Complex IV is both types of these devices. Fifty percent of the electrical potential that complex IV creates is as a proton pump. But, 50% of the electrical potential that complex IV…Under some conditions, mitochondrial ATP synthase has been observed to actually run in reverse. How would that situation affect the protonmotive force?
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