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In the name of GOD N i n a b a as j Bioenergetics h g Biological A Oxidation h e D r M . r i n o b Definition asa N i Bioenergetics n a j Energy Changes in Biochemical h g Reaction A h – Converting foodstuffs (fats, e r i proteins, carbohydrates) into n energyo M r. D b Metabolism asa N Metabolism is definedi as the total n a j of all cellular reactions h g that occur in the body; this A includes both the synthesis of h e r i molecules and the breakdown of n o molecules. M r. D b a Isothermic Reactions as N i In Non-Biological systems: Heat n a j energy is used for hperforming work. g A h e In Biological Systems: Chemical r i n Heat energy) is used for energyo(no M all biochemical reactions. .r D b a …Isothermic Reactions as N i Energy conserved in Living organisms: n a j By h g fuels Oxidation to metabolic A Stored as the high-energy bond of ATP h e r Provide energy for biological process i n o Muscle contraction, active ion transport M r. D b a Thermodynamic alaws s N i Interconvert different forms of energy n a surrounding and exchange with their j h g 1st Law: Energy can neither be created A nor be destroyed. h e r i It meansnenergy just converting o nd 2 Law: In spontaneous reactions the M total r. Entropy must be increased. D b a Overview of Bioenergetics as N i Metabolism n a j – Sum of all chemical reactions h g body that occur in A the – Anabolic h reactions e r i Synthesis of molecules n o – Catabolic reactions M r.Breakdown of molecules D b Gibbs Free Energyasa(ΔG) N i Energy available for useful work n a j h g ΔG=ΔH- TΔS A h e r i n ΔH= Changes in enthalpy or heat o M T= Temperature . r ΔS=Changes in entropy D b a Gibbs Free Energy as N i Negative ΔG=Exergonic n a j h g A h Positive ΔG=Endergonic e r i n o M . r ΔG=0 Equilibrium state D b a Standard Free Energy ΔG0 s a N i ΔG0=-RT LnKeq n a j h g A A+B C+D h e r i n Keq= Co* D/ A*B M r. D b a Metabolic reactions as N Endergonic reactions i n – Require energy to beaadded j – Endothermic h g • Exergonic reactions A – Release energy h e – Exothermic r i • Couplednreactions o – Liberation of energy in an exergonic M reaction .r drives an D endergonic reaction D r b a Coupled Reactions as N i n a j h g A h e r i n o M . Oxidation-Reduction b Reactions asa n a N i Oxidation – Removing an electron • Reduction – Addition of an electron • Oxidation and reduction are always coupled reactions • Often involves the transfer of hydrogen atoms rather than free electrons – Hydrogen atom contains one electron – A molecule that loses a hydrogen also loses an electron and therefore is oxidized • Importance of NAD and FAD h e D r M . r i n o j h g A Oxidation Reaction sab N i a The loss of electrons from n a substance. a j Or the gain of oxygen. h g A h e r i C6H12O6 o +n6O2 6CO2 + 6H2O + energy M r. D Oxidation glucose copyright cmassengale ATP 15 Reduction Reaction sab N i The gain of electronsnto a a j substance. h g Or the loss of oxygen. A a h e r i n o2 C6H12O6 + 6O M r. D Reduction 6CO2 + 6H2O + energy glucose copyright cmassengale ATP 16 Oxidation-Reduction Reaction Involving b a NAD and NADH as n a N i h e D r M . r i n o j h g A b a High-Energy Phosphates as N Adenosine triphosphate (ATP) i n – Consists of adenine, ribose, and three a j linked h g phosphates A • Synthesis h e • Breakdown r i ADP + Pi n ATP o + Energy ATP ATPase ADP + Pi M High-Energy Phosphates .r High-Energy Phosphates D D r b a Structure of ATP as N i n a j h g A h e r i n o M . Bioenergetics N i b a as Formation of ATP n a j – Phosphocreatine (PC) breakdown h g – DegradationAof glucose and glycogen eh r i Glycolysis n o Oxidative M formation of ATP D r. b a Formation of ATP as N Anaerobic pathways i n a j – Do not involve O2 h g – PC breakdown A and glycolysis h Aerobic pathways e r i n – Require O2 o M – Oxidative phosphorylation .r D b a Anaerobic ATP Production as N ATP-PC system i n – Immediate source ofaATP j h g • Glycolysis A – Glucose 2h pyruvic acid or 2 lactic acid e – Energy investment phase r i n Requires 2 ATP o – Energy generation phase M . Produces 4 ATP, 2 NADH, and 2 r pyruvate or 2 lactate D b a AEROBIC RESPIRATION as N 4 STAGES: i n a cytoplasm j Glycolysis h g A Mitochondrial Link reactionh matrix e r i n Kreb’soCycle Mitochondrial M matrix .r 4- D Oxidative Mitochondrial Phosphorylation 1. 2. 3. inner membrane (cristae) The Two Phases Glycolysis b a n a N i h e D r M . r i n o j h g A as Glycolysis: Energy b a Investment Phase as n a N i h e D r M . r i n o j h g A n a N i h e D r M . r i n o j h g A b a as Hydrogen and Electron b a Carrier Molecules as n a N i Transport hydrogens and associated electrons – To mitochondria for ATP generation (aerobic) – To convert pyruvic acid to lactic acid (anaerobic) • Nicotinamide adenine dinucleotide (NAD) • Flavin adenine dinucleotide (FAD) NAD + 2H+ NADH + H+ FAD + 2H+ FADH2 h e D r M . r i n o j h g A A Closer Look NADH is “Shuttled” into b Mitochondriaasa N NADH produced in glycolysis must be i n converted a j h back to NAD g – By converting pyruvic acid to lactic acid A h – By “shuttling” H+ into the mitochondria e • A specificirtransport system shuttles H+ n across the o mitochondrial membrane M . r – Located in the mitochondrial membrane D b a Aerobic ATP Production as Krebs cycle (citric acid cycle) i N – Pyruvic acid (3 C) is converted to acetyl-CoA (2 n a C) j h CO2 is given off g – Acetyl-CoA combines with oxaloacetate (4 C) to A form citrate (6 C) h – Citrate is metabolized to oxaloacetate e r i Two CO2 molecules given off n – Produces three molecules of NADH and one FADH o – Also forms one molecule of GTP M Produces one ATP r. D The Three Stages of Oxidative b a Phosphorylation as n a N i h e D r M . r i n o j h g A The Krebs Cycle n a N i h e D r M . r i n o j h g A b a as Regulation of CAC: Rate controlling enzymes: n a j h Isocitrate dehydrogenase g A a-keoglutaratedehydrogenase h e Regulation of activity by: r i n Substrate availability o M Product inhibition . r Allosteric inhibition or D Citrate synthatase activation by other intermediates N i b a as b a Aerobic ATP Production as N Electron transport chain i – Oxidative phosphorylation occurs in the n a mitochondria j h – Electrons removed from NADH and FADH are g passed along a series of carriers (cytochromes) to A produce ATP h e Each NADH r produces 2.5 ATP Each FADHiproduces 1.5 ATP n – Called the o chemiosmotic hypothesis – H+ from NADH and FADH are accepted by O2 to M .water form r Bioenergetics D Oxidative Phosphorylation:b Electron transport chain n a N i a as located on the membranes of the cristae of the mitochondria. The membranes contain a series of proteins, which are involved in the electron transport chain. Electrons are supplied in the form of reduced NAD and reduced FAD, which pass from the Krebs cycle in the matrix to the cristae. Electrons are passed from one protein to the next in a series of Redox reactions. At each transfer energy from the electrons is used to make ATP. The products of this process are low energy electrons and protons. Protons bind with oxygen to form water, and a total of 38 ATP molecules are generated. h e D r M . r i n o j h g A b a Oxidative phosphorylation as N i Also known as: n Terminal oxidationja h The electron transport chain g A A series of carrier molecules that h e transfer electrons along a chain , r i n producing ATP in the process. o The M electrons come from the . r hydrogen atoms released from D Kreb’s cycle Water is produced The Chemiosmotic b a Hypothesis of ATP Formation as N i Electron transport chainnresults in a pumping of H+ j h g ions across innerAmitochondrial membrane h e r – Resultsnini H+ gradient across o membrane M • Energy r. released to form ATP as H+ D diffuse ions back across the membrane n a N i h e D r M . r i n o j h g A b a as Sequence of Electron b a Carriers as n a N i h e D r M . r i n o j h g A Sequence of Electron Carriers b a n a N i h e D r M . r i n o j h g A as n a N i h e D r M . r i n o j h g A b a as Site of action of some inhibitors of electron transport N i b a as Inhibits electron flow in Complex I Prevents the utilization of NADH as a substrate. n a h e D r M . r i n o j h g A Inhibits electron flow from Cyt bH Cyanide (CN-), azide (N3- ) react with the ferric (Fe3+ ) form of heme a3. Carbon monoxide (CO): Inhibits the ferrous (Fe2+) form. n a N i h e D r M . r i n o j h g A b a as Stage Location Reactants Glycolysis Link reaction Kreb’s cycle Ox phosp Cytosol Glucose, ATP, NAD Phosphorylation, oxidation, gain of 2ATP Acetyl coenzyme A, carbon dioxide, NADH Decarboxylation, oxidation Acetyl coenzyme A, 4C compound, NAD, FAD, ADP NADH, FADH, carbon dioxide, ATP Oxidation, decarboxylation, gain of 1ATP r Hydrogen from NADH ATP, water, NAD Oxidation, phosphorylation Mitochondrial cristae D h e r i n o M . n a N i Other b a as details Pyruvate, NADH, ADP, ATP j h g A Mitochondrial Pyruvate, NAD, matrix coenzyme A Mitochondrial matrix Products In Cytosol n a N i h e D r M . r i n o j h g A b a as In Mitochondria b a Control of Bioenergetics as N Rate-limiting enzymes i n – An enzyme that regulates a the rate of a j metabolic h g pathway A • Modulators of h rate-limiting enzymes e r – Levels of ATP and ADP+Pi i n High levels o of ATP inhibit ATP production Low levels of ATP and high levels of ADP+Pi M r. ATP production stimulate D Example of a Rate-Limiting b a Enzyme as n a N i h e D r M . r i n o j h g A Study Questions n a N i b a as Briefly explain the concept of coupled reactions. 3. Define the following terms: (1) bioenergetics, (2)endergonic reactions, and (3) exergonic reactions. 4. Discuss the role of enzymes as catalysts. What is meant by the expression “energy of activation”? 5. Where do glycolysis, the Krebs cycle, and oxidative phosphorylation take place in the cell? h e D r M . r i n o j h g A …Study Questions n a N i b a as 7. What are the high-energy phosphates? Explain the statement that “ATP is the universal energy donor.” 8. Define the terms aerobic and anaerobic. 9. Briefly discuss the function of glycolysis in bioenergetics. What role does NAD play in glycolysis? 10. Discuss the operation of the Krebs cycle and the electron transport chain in the aerobic production of ATP. What is the function of NAD and FAD in these pathways? h e D r M . r i n o j h g A b a Thanks for your attention as N i n a j h g A h e r i n o M r. D