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ELECTRON TRANSPORT CHAIN Stage 4: How far have we come? • We began with our simple glucose molecule • Through the processes of... – GLYCOLYSIS – PYRUVATE OXIDATION – KREBS CYCLE ...we have used the energy stored in the C-C bonds of glucose to help ATP • Directly (substrate-level phosphorylation) • Indirectly (oxidative phosphorylation) Energy Totals • GLYCOLYSIS • PYRUVATE OXIDATION • KREBS CYCLE ATP USED ATP produced NADH produced FADH2 produced 2 4 2 0 ATP USED ATP produced NADH produced FADH2 produced 2 4 0 ATP USED ATP produced NADH produced FADH2 produced 2 10 2 4 6 So what’s the deal with ATP?? • C6H12O6 + 6O2 6CO2 + 6H2O + 36 ATP • We need to produce 36 ATP in Cell. Resp. • After 3 stages, we have only produced 6 ATP through substrate-level oxidation • Thus, there are 30 ATP left to create – We produce the remaining 30 ATP through oxidative phosphorylation in the ETC ELECTRON-TRANSPORT-CHAIN • In this step, we will utilize the energy provided by the electron carriers NADH and FADH2 •Extremely EXERGONIC ∆G = -2870 kJ/Mol How it works • NADH + FADH2 eventually transfer the electrons they carry to a series of proteins that are located in the inner membrane • The components of the ETC are arranged in order of increasing electronegativity • Thus, allowing the electrons to flow, or BE TRANSPORTED, between the compounds • Every step involves oxidation and reduction rxns. How it works • Every time an electron moves from one molecule to the next, free energy is released • The free energy is used to pump H+ ions, or PROTONS, from the mitochondrial matrix into the INTERMEMBRANE SPACE • The ETC needs a highly electronegative compound to oxidize the last protein – OXYGEN is used here, as it is one of the most electronegative compounds on earth How it works • An oxygen atom removes two é from the final protein complex • Oxygen then combines with 2 protons (H+) in the mitochondrial matrix to form an H2O molecule Diagram • The red path shows the path that é travel through the ETC • KNOW NAMES OF THESE MOLECULES How it works UBIQUINONE (Q) cytochrome C CYTOCHROME OXIDASE COMPLEX NADH DEHYDROGENASE CYTOCHROME b-c1 COMPLEX NADH + FADH2... Not so similar • NADH passes its electrons to the first protein complex – NADH DEHYDROGENASE • FADH2 passes its electrons to Q (or ubiquinone) • This distinction means that: – NADH = 3 H+ pumped out – FADH2 = 2 H+ pumped out • SO... – NADH produces 3 ATP – FADH2 produces 2 ATP NADH + FADH2... Not so similar • The NADH you produced in glycolysis works differently than the NADH produced in pyruvate oxidation and Krebs cycle – Why? • Glycolysis occurs in the cytoplasm, thus NADH has to travel through the double membrane of mitochondria – it can’t pass the inner membrane • NADH passes its é through a protein transport to FAD thus forming FADH2 ATP PRODUCTION • Electrochemical Gradient: A concentration gradient created by pumping ions into a space surrounded by a membrane that is impermeable to the ions – This is exactly what we are doing when we pump H+ ions into the intermembrane space using the ETC – Thus, the inner membrane becomes a H+ reservoir – An potential difference, or VOLTAGE, is created across the membrane • +ve charge in the intermembrane space • –ve charge in the mitochondria matrix + ------- - ATP PRODUCTION • H+ ions can not diffuse back through the innermembrane • They need to be pumped back by the transport protein ATP SYNTHASE • As H+ ions are passed through ATP SYNTHASE, the free energy of the gradient is reduced, thus releasing enough energy to produce ATP • ADP + Pi ATP ATP PRODUCTION • This process was coined: CHEMIOSMOSIS • ATP synthesized was caused by the ‘osmosis of H+ ions’ • Chemiosmosis is said to be COUPLED to the ETC Final Energy Tally Theoretical Yield vs. Actual Yield • It is possible that we will not always obtain 36 ATP for every glucose molecule that we used • 2 reasons: 1. Some H+ ions may make it through the inner mitochondrial membrane reducing the number of H+ ions that pass through ATP synthase. Some of the protons in the H+ reservoir might get used up in other cellular reactions 2.