Localization of Molecules and Functions Within the Mitochondrion. Indicate whether you would expect to find each of the following molecules or functions in the matrix (MA), the inner membrane (IM), the outer membrane (OM), the intermembrane space (IS), or not in the mitochondrion at all (NO). Write abbreviation in front of the molecules. No explanation is required. Succinate dehydrogenase Coenzyme A Conversion of lactate into pyruvate ATP synthase Malate dehydrogenase Pyruvate Citrate synthase Cristae Accumulation of a high proton concentration Pyruvate dehydrogenase

Localization of Molecules and Functions Within the Mitochondrion. Indicate whether you would expect to find each of the following molecules or functions in the matrix (MA), the inner membrane (IM), the outer membrane (OM), the intermembrane space (IS), or not in the mitochondrion at all (NO). Write abbreviation in front of the molecules. No explanation is required. Succinate dehydrogenase Coenzyme A Conversion of lactate into pyruvate ATP synthase Malate dehydrogenase Pyruvate Citrate synthase Cristae Accumulation of a high proton concentration Pyruvate dehydrogenase

Human Physiology: From Cells to Systems (MindTap Course List)

9th Edition

ISBN:9781285866932

Author:Lauralee Sherwood

Publisher:Lauralee Sherwood

Chapter2: Cell Physiology

Section: Chapter Questions

Problem 10RE: Using the answer code on the right, indicate which form of energy production is being described: 1....

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We have discussed the aerobic metabolism of glucose extensively in this class. To capture and use the energy in glucose to make ATP, we must utilize 4 different sequential pathways/steps. Starting with one glucose molecule and eventually ending with CO, H;O and ATP, list the 4 pathways/steps in order and tell me what molecules enter each pathway, and what the final products of each pathway are. Edit View Insert Format Tools Table 12pt v Paragraph v BIUAv ev Tov : I
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Leigh syndrome is characterized by psychomotor regression: that is, the progressive loss of mental andmovement abilities. Patients also suffer from lacticacidosis, a condition in which mitochondrial respiration is deficient, so their tissues metabolize glucoseanaerobically, leading to the buildup of lactate. Somepatients with Leigh syndrome have a mutation in themitochondrial gene MT-CO3, which encodes a subunit of the electron transport complex cytochromec oxidase. Other patients diagnosed with Leigh syndrome have a loss-of-function mutation in the nucleargene SURF1, which encodes a factor needed for theassembly of this same enzyme complex.a. How can the same symptoms result from mutationsin a mitochondrial gene and from mutations in anuclear gene?
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