BC368 Biochemistry of the Cell II Electron Transport Chain CH 19 (pp 731-747) March 19, 2015 http://www.science-groove.org/Now/Oxidative.html Case Study Last fall, Michael Phelps was pulled over in Baltimore after police spotted him driving erratically. A Breathalyzer test revealed that Phelps’ blood alcohol content was 0.14, well over the 0.08 legal limit. Redox Reactions 2 Cr2O72- + 3 C2H5OH + 16 H+ --> 4 Cr3+ + 3 CH3CO + 11 H2O Ethanol is oxidized; dichromate is reduced. Reaction can be monitored through a color change of the chromium species. Half Reactions Cr2O72- + 14 H+ + 6 e- --> 2 Cr3+ + 7 H2O Reduction (cathode) C2H5OH + H2O --> CH3COOH + 4 e- + 4 H+ Oxidation (anode) Overall: 2 Cr2O72- + 3 C2H5OH + 16 H+ --> 4 Cr3+ + 3 CH3COOH + 11 H2O Higher tendency for reduction Half Reactions Standard reduction potentials are for reduction. In general, ’cell = ’cathode - ’anode Reduced Lower tendency for reduction Oxidized Half Reactions Cr2O72- + 14 H+ + 6 e- --> 2 Cr3+ + 7 H2O Reduction (cathode); = 1.33 V C2H5OH --> CH3COOH + 2 e- + 2 H+ Oxidation (anode); = 0.058 V (for the reduction) cell = 1.33 V - 0.058 V = 1.27 V Half Reactions In general, ’cell = ’cathode - ’anode Reduced Oxidized ’cell > 0 is favorable DG’ = -nF’cell In-Class Problem ATP is made through oxidative phosphorylation, powered by the free energy released from electron transfer from NADH to O2. a) Given the following reduction potentials, calculate the available standard free energy from this process. NAD+ + H+ + 2 e- NADH E’º = -0.32 V 1/2 O2 + 2 H+ + 2 e- H2O E’º = 0.82 V b) If three ATP ’ s are synthesized per electron pair transferred, what is the efficiency of the process? ETC Video Chemiosmotic Mechanism Electron transport chain sets up an H+ gradient (proton motive force). Energy of the pmf is harnessed to make ATP. Fig 19-2 Mitochondrion Double membrane, with inner membrane very impermeable TCA occurs in the matrix ETC in the inner membrane Cardiolipin Case Study The patient was delivered by emergency C-section at 31 weeks of gestation. He required intubation in the delivery room because of apnea and bradycardia and was treated in the Neonatal Intensive Care Unit. A follow-up chest X-ray taken at 1 month of age showed an enlarged heart and prompted a cardiology consult. Although there was no clinical evidence of congestive heart failure, the cardiac ultrasound showed a significant decrease in left ventricular function. The family history was significant in that the patient’s maternal uncle died from sudden infant death syndrome. At 11 months of age, the patient’s mother was concerned about his poor weight gain and development because he was not yet sitting alone. Case Study At his 20th-month visit, persistent muscle weakness, growth delays, and congestive cardiomyopathy led the cardiologist to make a genetics referral. Two days following this clinic visit, however, the patient presented to his primary care provider with cough, wheezing, runny nose, and one day of fever and mental status change. His condition deteriorated, requiring intubation, and he was transferred to the Pediatric Intensive Care Unit. The diagnosis was pneumonia, and severe lactic acidosis was found. He failed to respond to aggressive treatment and died from repeated ventricular fibrillation that occurred 10 days later. Autopsy limited to the heart was performed. The gross and microscopic findings were characteristic of Barth syndrome. The heart weighed 100 g (average for his age is 56 g, and 100 g is the average for a 7-year-old). Case Study A small number of boys suffer from Barth syndrome (~50 births/year in the United States). Cardiolipin Barth’s results from a mutation on the X chromosome in the gene coding for taffazin, an enzyme involved in the biosynthesis of cardiolipin. Patients with Barth syndrome have abnormal mitochondria and cannot maintain normal rates of ATP production. These patients develop lifethreatening cardiomyopathy and muscle weakness. Electron transport chain ETC carriers: Coenzyme Q Mobile electron carrier within the bilayer 1- or 2electron acceptor Fig 19-3 ETC carriers: FMN Prosthetic group of ETC protein (complex I) 1- or 2-electron acceptor ETC carriers: Cytochromes Heme proteins Most are integral proteins Cytochrome c is a soluble peripheral protein ETC carriers: Iron-sulfur proteins Fig 19-5 ETC carriers: Copper centers CuA center CuB center Electron Transport Chain: Proteins Electron Transport Chain ~Fig 19-16 Complex I Alternate Entries Fig 19-8 Alternate Entries Complex II (aka succinate dehydrogenase) Alternate Entries Fig 19-8 Alternate Entries Fig 19-8 Electron Transport Chain Complex III Complex III Fig 19-11 Electron Transport Chain Complex IV Fig 19-14 Complex IV Electron Transport Chain Succinate dehydrogenase Electrons flow from carriers with low to high reduction potential. This is energetically downhill. Per electron pair: 4 H+ in Electron Transport Chain 4 H+ out Succinate dehydrogenase 4 H+ in 4 H+ out Some carriers pump protons. 2 H+ in 2 H+ out Flow direction Flow direction Inhibitors of electron transport Fig 19-6 Case Study Four carriers (a, b, c, d) are required for respiration in a novel bacterial electron-transport system. In the presence of substrate and O2, three different inhibitors block respiration as shown. What is the order of carriers? Inhibitor 1 2 3 a b c d + + + - - + + + “+” = fully oxidized; “-” = fully reduced Q Cycle Q Cycle Q Cycle O2 consumption as a measure of electron transport An oxygen electrode can measure O2 consumption in respiring mitochondria. O2 consumption as a measure of electron transport Substrate added Substrate consumed An oxygen electrode can measure O2 consumption in respiring mitochondria. O2 consumption as a measure of electron transport An oxygen electrode can measure O2 consumption in respiring mitochondria. Coupling of electron transport and ATP synthesis Data can be reported as O2 concentration or O2 consumption. Coupling of electron transport and ATP synthesis Fig 19-20 Coupling of electron transport and ATP synthesis Fig 19-20