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PowerPoint® Lecture Slides prepared by Vince Austin, Bluegrass Technical and Community College CHAPTER Elaine N. Marieb Katja Hoehn 24 PART A Human Anatomy & Physiology SEVENTH EDITION Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Nutrition, Metabolism, and Body Temperature Regulation Nutrition    Nutrient – a substance that promotes normal growth, maintenance, and repair Major nutrients – carbohydrates, lipids, and proteins Other nutrients – vitamins and minerals (and technically speaking, water) Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings USDA Food Guide Pyramid Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.1a Nutrition Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.1b Carbohydrates  Complex carbohydrates (starches) are found in bread, cereal, flour, pasta, nuts, and potatoes  Simple carbohydrates (sugars) are found in soft drinks, candy, fruit, and ice cream Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Carbohydrates  Glucose is the molecule ultimately used by body cells to make ATP  Neurons and RBCs rely almost entirely upon glucose to supply their energy needs  Excess glucose is converted to glycogen or fat and stored Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Carbohydrates  The minimum amount of carbohydrates needed to maintain adequate blood glucose levels is 100 grams per day  Starchy foods and milk have nutrients such as vitamins and minerals in addition to complex carbohydrates  Refined carbohydrate foods (candy and soft drinks) provide energy sources only and are referred to as “empty calories” Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Lipids    The most abundant dietary lipids, triglycerides, are found in both animal and plant foods Essential fatty acids – linoleic and linolenic acid, found in most vegetables, must be ingested Dietary fats:  Help the body to absorb vitamins  Are a major energy fuel of hepatocytes and skeletal muscle  Are a component of myelin sheaths and all cell membranes Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Lipids  Fatty deposits in adipose tissue provide:  A protective cushion around body organs  An insulating layer beneath the skin  An easy-to-store concentrated source of energy Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Lipids   Prostaglandins function in:  Smooth muscle contraction  Control of blood pressure  Inflammation Cholesterol stabilizes membranes and is a precursor of bile salts and steroid hormones Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Lipids: Dietary Requirements  Higher for infants and children than for adults  The American Heart Association suggests that:  Fats should represent less than 30% of one’s total caloric intake  Saturated fats should be limited to 10% or less of one’s total fat intake  Daily cholesterol intake should not exceed 200 mg Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Proteins   Complete proteins that meet all the body’s amino acid needs are found in eggs, milk, milk products, meat, and fish Incomplete proteins are found in legumes, nuts, seeds, grains, and vegetables Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Proteins   Proteins supply:  Essential amino acids, the building blocks for nonessential amino acids  Nitrogen for nonprotein nitrogen-containing substances Daily intake should be approximately 0.8g/kg of body weight Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Proteins: Synthesis and Hydrolysis  All-or-none rule   All amino acids needed must be present at the same time for protein synthesis to occur Adequacy of caloric intake  Protein will be used as fuel if there is insufficient carbohydrate or fat available Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Proteins: Synthesis and Hydrolysis  Nitrogen balance     The rate of protein synthesis equals the rate of breakdown and loss Positive – synthesis exceeds breakdown (normal in children and tissue repair) Negative – breakdown exceeds synthesis (e.g., stress, burns, infection, or injury) Hormonal control  Anabolic hormones accelerate protein synthesis Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Essential Amino Acids Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.2 Vitamins  Organic compounds needed for growth and good health  They are crucial in helping the body use nutrients and often function as coenzymes  Only vitamins D, K, and B are synthesized in the body; all others must be ingested  Water-soluble vitamins (B-complex and C) are absorbed in the gastrointestinal tract  B12 additionally requires gastric intrinsic factor to be absorbed Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Vitamins  Fat-soluble vitamins (A, D, E, and K) bind to ingested lipids and are absorbed with their digestion products  Vitamins A, C, and E also act in an antioxidant cascade Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Minerals  Seven minerals are required in moderate amounts  Calcium, phosphorus, potassium, sulfur, sodium, chloride, and magnesium  Dozens are required in trace amounts  Minerals work with nutrients to ensure proper body functioning  Calcium, phosphorus, and magnesium salts harden bone Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Minerals  Sodium and chloride help maintain normal osmolarity, water balance, and are essential in nerve and muscle function  Uptake and excretion must be balanced to prevent toxic overload Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Metabolism   Metabolism – all chemical reactions necessary to maintain life Cellular respiration – food fuels are broken down within cells and some of the energy is captured to produce ATP   Anabolic reactions – synthesis of larger molecules from smaller ones Catabolic reactions – hydrolysis of complex structures into simpler ones Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Metabolism  Enzymes shift the high-energy phosphate groups of ATP to other molecules  These phosphorylated molecules are activated to perform cellular functions Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Stages of Metabolism  Energy-containing nutrients are processed in three major stages    Digestion – breakdown of food; nutrients are transported to tissues Anabolism and formation of catabolic intermediates where nutrients are:  Built into lipids, proteins, and glycogen  Broken down by catabolic pathways to pyruvic acid and acetyl CoA Oxidative breakdown – nutrients are catabolized to carbon dioxide, water, and ATP Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.3 Oxidation-Reduction (Redox) Reactions  Oxidation occurs via the gain of oxygen or the loss of hydrogen  Whenever one substance is oxidized, another substance is reduced  Oxidized substances lose energy  Reduced substances gain energy  Coenzymes act as hydrogen (or electron) acceptors  Two important coenzymes are nicotinamide adenine dinucleotide (NAD+) and flavin adenine dinucleotide (FAD) Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Mechanisms of ATP Synthesis: Substrate-Level Phosphorylation  High-energy phosphate groups are transferred directly from phosphorylated substrates to ADP  ATP is synthesized via substrate-level phosphorylation in glycolysis and the Krebs cycle Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.4a Mechanisms of ATP Synthesis: Oxidative Phosphorylation  Uses the chemiosmotic process whereby the movement of substances across a membrane is coupled to chemical reactions Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Mechanisms of ATP Synthesis: Oxidative Phosphorylation  Is carried out by the electron transport proteins in the cristae of the mitochondria  Nutrient energy is used to pump hydrogen ions into the intermembrane space  A steep diffusion gradient across the membrane results  When hydrogen ions flow back across the membrane through ATP synthase, energy is captured and attaches phosphate groups to ADP (to make ATP) Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Mechanisms of ATP Synthesis: Oxidative Phosphorylation Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.4b Carbohydrate Metabolism  Since all carbohydrates are transformed into glucose, it is essentially glucose metabolism    Oxidation of glucose is shown by the overall reaction: C6H12O6 + 6O2  6H2O + 6CO2 + 36 ATP + heat Glucose is catabolized in three pathways  Glycolysis  Krebs cycle  The electron transport chain and oxidative phosphorylation Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Carbohydrate Catabolism Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.5 Glycolysis   A three-phase pathway in which:  Glucose is oxidized into pyruvic acid  NAD+ is reduced to NADH + H+  ATP is synthesized by substrate-level phosphorylation Pyruvic acid:  Moves on to the Krebs cycle in an aerobic pathway  Is reduced to lactic acid in an anaerobic environment Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Glycolysis Glycolysis ATP Krebs cycle ATP Electron transport chain and oxidative phosphorylation ATP Glucose Phase 1 Sugar activation Key: = Carbon atom Pi = Inorganic phosphate 2 ATP 2 ADP Fructose-1,6bisphosphate P P Phase 2 Sugar Dihydroxyacetone cleavage phosphate P Pi Glyceraldehyde phosphate P 2 NAD+ 4 ADP 2 NADH+H+ Phase 3 Sugar oxidation and formation of ATP 4 ATP 2 Pyruvic acid 2 NADH+H+ O2 To Krebs cycle (aerobic pathway) Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings O2 2 NAD+ 2 Lactic acid Figure 24.6 Glycolysis Glycolysis ATP Krebs cycle ATP Electron transport chain and oxidative phosphorylation ATP Glucose Phase 1 Sugar activation 2 ATP 2 ADP Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Key: = Carbon atom Pi = Inorganic phosphate Figure 24.6 Glycolysis Glycolysis ATP Krebs cycle ATP Electron transport chain and oxidative phosphorylation ATP Glucose Phase 1 Sugar activation 2 ATP 2 ADP Fructose-1,6bisphosphate P P Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Key: = Carbon atom Pi = Inorganic phosphate Figure 24.6 Glycolysis Glycolysis ATP Krebs cycle ATP Electron transport chain and oxidative phosphorylation ATP Glucose Phase 1 Sugar activation 2 ATP 2 ADP Fructose-1,6bisphosphate P P Phase 2 Sugar Dihydroxyacetone cleavage phosphate P Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Key: = Carbon atom Pi = Inorganic phosphate Glyceraldehyde phosphate P Figure 24.6 Glycolysis Glycolysis ATP Krebs cycle ATP Electron transport chain and oxidative phosphorylation ATP Glucose Phase 1 Sugar activation 2 ATP 2 ADP Fructose-1,6bisphosphate P P Phase 2 Sugar Dihydroxyacetone cleavage phosphate P Pi Key: = Carbon atom Pi = Inorganic phosphate Glyceraldehyde phosphate P 2 NAD+ 2 NADH+H+ Phase 3 Sugar oxidation and formation of ATP Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.6 Glycolysis Glycolysis ATP Krebs cycle ATP Electron transport chain and oxidative phosphorylation ATP Glucose Phase 1 Sugar activation 2 ATP 2 ADP Fructose-1,6bisphosphate P P Phase 2 Sugar Dihydroxyacetone cleavage phosphate P Pi Key: = Carbon atom Pi = Inorganic phosphate Glyceraldehyde phosphate P 2 NAD+ 4 ADP 2 NADH+H+ Phase 3 Sugar oxidation and formation of ATP 4 ATP 2 Pyruvic acid Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.6 Glycolysis Glycolysis ATP Krebs cycle ATP Electron transport chain and oxidative phosphorylation ATP Glucose Phase 1 Sugar activation 2 ATP 2 ADP Fructose-1,6bisphosphate P P Phase 2 Sugar Dihydroxyacetone cleavage phosphate P Pi Key: = Carbon atom Pi = Inorganic phosphate Glyceraldehyde phosphate P 2 NAD+ 4 ADP 2 NADH+H+ Phase 3 Sugar oxidation and formation of ATP 4 ATP 2 Pyruvic acid O2 To Krebs cycle (aerobic pathway) Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.6 Glycolysis Glycolysis ATP Krebs cycle ATP Electron transport chain and oxidative phosphorylation ATP Glucose Phase 1 Sugar activation Key: = Carbon atom Pi = Inorganic phosphate 2 ATP 2 ADP Fructose-1,6bisphosphate P P Phase 2 Sugar Dihydroxyacetone cleavage phosphate P Pi Glyceraldehyde phosphate P 2 NAD+ 4 ADP 2 NADH+H+ Phase 3 Sugar oxidation and formation of ATP 4 ATP 2 Pyruvic acid 2 NADH+H+ O2 To Krebs cycle (aerobic pathway) Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings O2 2 NAD+ 2 Lactic acid Figure 24.6 Glycolysis: Phase 1 and 2  Phase 1: Sugar activation   Two ATP molecules activate glucose into fructose-1,6-diphosphate Phase 2: Sugar cleavage  Fructose-1,6-bisphosphate is cleaved into two 3-carbon isomers  Bishydroxyacetone phosphate  Glyceraldehyde 3-phosphate Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Glycolysis: Phase 3  Phase 3: Oxidation and ATP formation  The 3-carbon sugars are oxidized (reducing NAD+)  Inorganic phosphate groups (Pi) are attached to each oxidized fragment  The terminal phosphates are cleaved and captured by ADP to form four ATP molecules Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Glycolysis: Phase 3  The final products are:  Two pyruvic acid molecules  Two NADH + H+ molecules (reduced NAD+)  A net gain of two ATP molecules Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Krebs Cycle: Preparatory Step  Occurs in the mitochondrial matrix and is fueled by pyruvic acid and fatty acids Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Krebs Cycle: Preparatory Step  Pyruvic acid is converted to acetyl CoA in three main steps:  Decarboxylation  Carbon is removed from pyruvic acid  Carbon dioxide is released Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Krebs Cycle: Preparatory Step   Oxidation  Hydrogen atoms are removed from pyruvic acid  NAD+ is reduced to NADH + H+ Formation of acetyl CoA – the resulting acetic acid is combined with coenzyme A, a sulfur-containing coenzyme, to form acetyl CoA Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Krebs Cycle   An eight-step cycle in which each acetic acid is decarboxylated and oxidized, generating:  Three molecules of NADH + H+  One molecule of FADH2  Two molecules of CO2  One molecule of ATP For each molecule of glucose entering glycolysis, two molecules of acetyl CoA enter the Krebs cycle PLAY Krebs Cycle Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Cytosol Pyruvic acid from glycolysis Glycolysis ATP Krebs cycle Electron transport chain and oxidative phosphorylation NAD+ CO2 CoA Acetyl CoA ATP Mitochondrion (fluid matrix) NADH+H+ ATP Oxaloacetic acid (pickup molecule) NADH+H+ Citric acid CoA (initial reactant) NAD+ Isocitric acid Malic acid NAD+ Krebs cycle CO2 NADH+H+ a-Ketoglutaric acid Fumaric acid CO2 FADH2 FAD Key: Succinic acid Succinyl-CoA CoA NAD+ NADH+H+ CoA = Carbon atom GTP GDP + Pi ADP ATP Pi = Inorganic phosphate CoA = Coenzyme A Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.7 Pyruvic acid from glycolysis Glycolysis ATP Krebs cycle Electron transport chain and oxidative phosphorylation ATP CO2 CoA Acetyl CoA Cytosol NAD+ NADH+H+ Mitochondrion (fluid matrix) ATP Key: = Carbon atom Pi = Inorganic phosphate CoA = Coenzyme A Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.7 Pyruvic acid from glycolysis Glycolysis ATP Krebs cycle Electron transport chain and oxidative phosphorylation ATP Cytosol NAD+ CO2 CoA Acetyl CoA NADH+H+ Mitochondrion (fluid matrix) ATP Oxaloacetic acid (pickup molecule) Citric acid CoA (initial reactant) Krebs cycle Key: = Carbon atom Pi = Inorganic phosphate CoA = Coenzyme A Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.7 Cytosol Pyruvic acid from glycolysis Glycolysis ATP Krebs cycle Electron transport chain and oxidative phosphorylation ATP NAD+ CO2 CoA Acetyl CoA NADH+H+ Mitochondrion (fluid matrix) ATP Oxaloacetic acid (pickup molecule) Citric acid CoA (initial reactant) Isocitric acid Krebs cycle Key: = Carbon atom Pi = Inorganic phosphate CoA = Coenzyme A Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.7 Cytosol Pyruvic acid from glycolysis Glycolysis ATP Krebs cycle Electron transport chain and oxidative phosphorylation ATP NAD+ CO2 CoA Acetyl CoA NADH+H+ Mitochondrion (fluid matrix) ATP Oxaloacetic acid (pickup molecule) Citric acid CoA (initial reactant) Isocitric acid NAD+ Krebs cycle CO2 NADH+H+ a-Ketoglutaric acid Key: = Carbon atom Pi = Inorganic phosphate CoA = Coenzyme A Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.7 Cytosol Pyruvic acid from glycolysis Glycolysis ATP Krebs cycle Electron transport chain and oxidative phosphorylation ATP NAD+ CO2 CoA Acetyl CoA Mitochondrion (fluid matrix) NADH+H+ ATP Oxaloacetic acid (pickup molecule) Citric acid CoA (initial reactant) Isocitric acid NAD+ Krebs cycle CO2 NADH+H+ a-Ketoglutaric acid CO2 Succinyl-CoA CoA NAD+ NADH+H+ Key: = Carbon atom Pi = Inorganic phosphate CoA = Coenzyme A Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.7 Cytosol Pyruvic acid from glycolysis Glycolysis ATP Krebs cycle Electron transport chain and oxidative phosphorylation ATP NAD+ CO2 CoA Acetyl CoA Mitochondrion (fluid matrix) NADH+H+ ATP Oxaloacetic acid (pickup molecule) Citric acid CoA (initial reactant) Isocitric acid NAD+ Krebs cycle CO2 NADH+H+ a-Ketoglutaric acid CO2 Succinic acid Key: Succinyl-CoA CoA NAD+ NADH+H+ CoA = Carbon atom GTP GDP + Pi ADP ATP Pi = Inorganic phosphate CoA = Coenzyme A Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.7 Cytosol Pyruvic acid from glycolysis Glycolysis ATP Krebs cycle Electron transport chain and oxidative phosphorylation NAD+ CO2 CoA Acetyl CoA ATP Mitochondrion (fluid matrix) NADH+H+ ATP Oxaloacetic acid (pickup molecule) Citric acid CoA (initial reactant) Isocitric acid NAD+ Krebs cycle CO2 NADH+H+ a-Ketoglutaric acid Fumaric acid CO2 FADH2 FAD Key: Succinic acid Succinyl-CoA CoA NAD+ NADH+H+ CoA = Carbon atom GTP GDP + Pi ADP ATP Pi = Inorganic phosphate CoA = Coenzyme A Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.7 Cytosol Pyruvic acid from glycolysis Glycolysis ATP Krebs cycle Electron transport chain and oxidative phosphorylation NAD+ CO2 CoA Acetyl CoA ATP Mitochondrion (fluid matrix) NADH+H+ ATP Oxaloacetic acid (pickup molecule) Citric acid CoA (initial reactant) Isocitric acid Malic acid NAD+ Krebs cycle CO2 NADH+H+ a-Ketoglutaric acid Fumaric acid CO2 FADH2 FAD Key: Succinic acid Succinyl-CoA CoA NAD+ NADH+H+ CoA = Carbon atom GTP GDP + Pi ADP ATP Pi = Inorganic phosphate CoA = Coenzyme A Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.7 Cytosol Pyruvic acid from glycolysis Glycolysis ATP Krebs cycle Electron transport chain and oxidative phosphorylation NAD+ CO2 CoA Acetyl CoA ATP Mitochondrion (fluid matrix) NADH+H+ ATP Oxaloacetic acid (pickup molecule) NADH+H+ Citric acid CoA (initial reactant) NAD+ Isocitric acid Malic acid NAD+ Krebs cycle CO2 NADH+H+ a-Ketoglutaric acid Fumaric acid CO2 FADH2 FAD Key: Succinic acid Succinyl-CoA CoA NAD+ NADH+H+ CoA = Carbon atom GTP GDP + Pi ADP ATP Pi = Inorganic phosphate CoA = Coenzyme A Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.7 Electron Transport Chain   Food (glucose) is oxidized and the released hydrogens:  Are transported by coenzymes NADH and FADH2  Enter a chain of proteins bound to metal atoms (cofactors)  Combine with molecular oxygen to form water  Release energy The energy released is harnessed to attach inorganic phosphate groups (Pi) to ADP, making ATP by oxidative phosphorylation Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Mechanism of Oxidative Phosphorylation  The hydrogens delivered to the chain are split into protons (H+) and electrons   The protons are pumped across the inner mitochondrial membrane by:  NADH dehydrogenase (FMN, Fe-S)  Cytochrome b-c1  Cytochrome oxidase (a-a3) The electrons are shuttled from one acceptor to the next Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Mechanism of Oxidative Phosphorylation  Electrons are delivered to oxygen, forming oxygen ions  Oxygen ions attract H+ to form water  H+ pumped to the intermembrane space:  Diffuses back to the matrix via ATP synthase  Releases energy to make ATP PLAY InterActive Physiology ®: Muscular System: Muscular Metabolism Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Glycolysis Krebs cycle Electron transport chain and oxidative phosphorylation ATP ATP ATP H+ H+ H+ H+ Intermembrane space Core Cyt c e- eQ 1 3 2 Inner mitochondrial membrane 2 H+ + FADH2 NADH + Mitochondrial matrix O2 H2O FAD ATP ADP + Pi H+ (carrying efrom food) 1 2 NAD + H+ Electron Transport Chain Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings ATP Synthase Figure 24.8 Glycolysis Krebs cycle Electron transport chain and oxidative phosphorylation ATP ATP ATP H+ Core Intermembrane space Cyt c Q 1 3 2 Inner mitochondrial membrane NADH + H+ (carrying efrom food) Mitochondrial matrix NAD + Electron Transport Chain Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.8 Glycolysis Krebs cycle Electron transport chain and oxidative phosphorylation ATP ATP ATP H+ H+ Core Intermembrane space Cyt c eQ 1 3 2 Inner mitochondrial membrane FADH2 NADH + (carrying efrom food) Mitochondrial matrix FAD H+ NAD + Electron Transport Chain Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.8 Glycolysis Krebs cycle Electron transport chain and oxidative phosphorylation ATP ATP ATP H+ H+ H+ Core Intermembrane space Cyt c e- eQ 1 3 2 Inner mitochondrial membrane FADH2 NADH + (carrying efrom food) Mitochondrial matrix FAD H+ NAD + Electron Transport Chain Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.8 Glycolysis Krebs cycle Electron transport chain and oxidative phosphorylation ATP ATP ATP H+ H+ H+ H+ Intermembrane space Core Cyt c e- eQ 1 3 2 Inner mitochondrial membrane FADH2 NADH + (carrying efrom food) Mitochondrial matrix FAD H+ NAD + Electron Transport Chain Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings ATP Synthase Figure 24.8 Glycolysis Krebs cycle Electron transport chain and oxidative phosphorylation ATP ATP ATP H+ H+ H+ H+ Intermembrane space Core Cyt c e- eQ 1 3 2 Inner mitochondrial membrane FADH2 NADH + (carrying efrom food) Mitochondrial matrix FAD ATP ADP + Pi H+ NAD + H+ Electron Transport Chain Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings ATP Synthase Figure 24.8 Glycolysis Krebs cycle Electron transport chain and oxidative phosphorylation ATP ATP ATP H+ H+ H+ H+ Intermembrane space Core Cyt c e- eQ 1 3 2 Inner mitochondrial membrane 2 H+ + FADH2 NADH + Mitochondrial matrix O2 H2O FAD ATP ADP + Pi H+ (carrying efrom food) 1 2 NAD + H+ Electron Transport Chain Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings ATP Synthase Figure 24.8 Electronic Energy Gradient  The transfer of energy from NADH + H+ and FADH2 to oxygen releases large amounts of energy  This energy is released in a stepwise manner through the electron transport chain Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Electronic Energy Gradient   The electrochemical proton gradient across the inner membrane:  Creates a pH gradient  Generates a voltage gradient These gradients cause H+ to flow back into the matrix via ATP synthase PLAY Electron Transport Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.9 ATP Synthase  The enzyme consists of three parts: a rotor, a knob, and a rod  Current created by H+ causes the rotor and rod to rotate  This rotation activates catalytic sites in the knob where ADP and Pi are combined to make ATP Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Structure of ATP Synthase Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.10 Summary of ATP Production Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.11 Glycogenesis and Glycogenolysis   Glycogenesis – formation of glycogen when glucose supplies exceed cellular need for ATP synthesis Glycogenolysis – breakdown of glycogen in response to low blood glucose Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.12 Gluconeogenesis  The process of forming sugar from noncarbohydrate molecules  Takes place mainly in the liver  Protects the body, especially the brain, from the damaging effects of hypoglycemia by ensuring ATP synthesis can continue Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Lipid Metabolism  Most products of fat metabolism are transported in lymph as chylomicrons  Lipids in chylomicrons are hydrolyzed by plasma enzymes and absorbed by cells  Only neutral fats are routinely oxidized for energy Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Lipid Metabolism  Catabolism of fats involves two separate pathways  Glycerol pathway  Fatty acids pathway Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Lipid Metabolism  Glycerol is converted to glyceraldehyde phosphate  Glyceraldehyde is ultimately converted into acetyl CoA  Acetyl CoA enters the Krebs cycle Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Lipid Metabolism  Fatty acids undergo beta oxidation which produces:  Two-carbon acetic acid fragments, which enter the Krebs cycle  Reduced coenzymes, which enter the electron transport chain Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Lipid Metabolism Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.13 Lipogenesis and Lipolysis  Excess dietary glycerol and fatty acids undergo lipogenesis to form triglycerides  Glucose is easily converted into fat since acetyl CoA is:  An intermediate in glucose catabolism  The starting molecule for the synthesis of fatty acids Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Lipogenesis and Lipolysis  Lipolysis, the breakdown of stored fat, is essentially lipogenesis in reverse  Oxaloacetic acid is necessary for the complete oxidation of fat  Without it, acetyl CoA is converted into ketones (ketogenesis) Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Lipogenesis and Lipolysis Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.14 Lipid Metabolism: Synthesis of Structural Materials  Phospholipids are important components of myelin and cell membranes Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Lipid Metabolism: Synthesis of Structural Materials   The liver:  Synthesizes lipoproteins for transport of cholesterol and fats  Makes tissue factor, a clotting factor  Synthesizes cholesterol for acetyl CoA  Uses cholesterol to form bile salts Certain endocrine organs use cholesterol to synthesize steroid hormones Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Protein Metabolism   Excess dietary protein results in amino acids being:  Oxidized for energy  Converted into fat for storage Amino acids must be deaminated prior to oxidation for energy Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Protein Metabolism   Deaminated amino acids are converted into:  Pyruvic acid  One of the keto acid intermediates of the Krebs cycle These events occur as transamination, oxidative deamination, and keto acid modification Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Amino Acid Oxidation Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Figure 24.15
 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 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