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Electron Transport System Electron Transport System

Electron Transport System - PowerPoint Presentation

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Electron Transport System - PPT Presentation

ETS Dr Keshav Singh Associate Professor Department of Zoology DDU Gorakhpur University The NADH and FADH 2  formed in  glycolysis   TCA cycle  and fatty acid oxidation are energyrich molecules because they contain a pair of electrons that have high transfer potential ID: 1044174

complex electrons atp electron electrons complex electron atp transport cytochrome chain nadh membrane transfer energy protons dehydrogenase gradient respiratory

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1. Electron Transport System(ETS)Dr. Keshav SinghAssociate ProfessorDepartment of ZoologyD.D.U Gorakhpur University

2. The NADH and FADH2 formed in glycolysis, TCA cycle and fatty acid oxidation are energy-rich molecules because they contain a pair of electrons that have high transfer potential.ATP is generated as a result of the energy produced when electrons from NADH and FADH2 are passed to molecular oxygen by a series of electron carriers, collectively known as the electron transport chain (ETC).The electron transport chain is also called the Cytochrome oxidase system or as the Respiratory chain.The components of the chain include FMN, Fe–S centers, coenzyme Q, and a series of cytochromes (b, c1, c, and aa3).The energy derived from the transfer of electrons through the electron transport chain is used to pump protons across the inner mitochondrial membrane from the matrix to the cytosolic side.As a result, an electrochemical gradient is generated, consisting of a proton gradient and a membrane potential.The energy created by the formation of this gradient is then harnessed to form ATP as the protons travel down their gradient into the matrix through the ATP synthase channel.The oxidation of 1 mole of NADH generates approximately 2.5 moles of ATP, whereas the oxidation of 1 mole of FADH2 generates approximately 1.5 moles of ATP.Because energy generated by the transfer of electrons through the electron transport chain to O2 is used in the production of ATP, the overall process is known as oxidative phosphorylation.Thus, the electron transport and ATP production occur simultaneously and are tightly coupled.

3. The electron transport chain is a series of four protein complexes that couple redox reactions, creating an electrochemical gradient that leads to the creation of ATP in a complete system named oxidative phosphorylation. It occurs in mitochondria in both cellular respiration.ETS also known as chemiosmotic mechanism.Oxidation of hydrogen in mitochondriaHydrogen atoms ionized and split in electron(e-) and proton(H+).Electrons are very rich in free energy.ETS sequences are called “respiratory chain or assemblies”.Each assemblies consists of electron carrier protein which is divisible in to four groups or multiprotein complexes.Assemblies have six components- 1.NADH-dehydrogenase complex 2. Succinate- dehydrogenase complex 3.Co-enzyme-Q( CoQ) or ubiquinone 4.Ubiquinone-cytochrome c-reductase complex 5. Cytochrome –c 6.Cytochrome c-oxidase complex

4.

5. The electron transport chain, and site of oxidative phosphorylation is found on the inner mitochondrial membrane. The energy stored from the process of respiration in reduced compounds (such as NADH and FADH) is used by the electron transport chain to pump protons into the inter membrane space, generating the electrochemical gradient over the inner mitochrondrial membrane. In photosynthetic eukaryotes, the electron transport chain is found on the thylakoid membrane. Here, light energy drives the reduction of components of the electron transport chain and therefore causes subsequent synthesis of ATP. In bacteria, the electron transport chain can vary over species but it always constitutes a set of redox reactions that are coupled to the synthesis of ATP, through the generation of an electrochemical gradient, and oxidative phosphorylation through ATP synthase.

6. Components of the Electron Transport ChainComplex I (NADH dehydrogenase)It contains FMN, which accepts 2 electrons and H + from 2 NADH to become the reduced form of FMNH2; also contains iron atoms, which assist in the transfer of the e − and H + to coenzyme Q.Complex II (Succinate dehydrogenase)Contains iron and succinate, which oxidizes FAD to form FADH2Coenzyme QAccepts electrons from FMNH2 (complex I) and FADH2 (complex II) and transfers electrons to complex III.Complex III (cytochrome b)It contains heme group, in which the Fe 3+ accepts the electrons from coenzyme Q to become Fe 2+. Transfers electrons to cytochrome c.Cytochrome cIt contains the heme group, in which the Fe 3+ accepts the electrons from complex III to become Fe 2+. Transfers electrons to complex IV.Complex IV (cytochrome a) It contains the heme group, in which the Fe 3+ accepts electrons from cytochrome c to become Fe 2+. Transfers electrons to O2, which is combined with hydrogen to form H2O.Complex V (ATP synthase)It contains a proton channel that allows for protons to cross into the matrix, using the proton gradient energy to form ATP.

7. Major Steps in Electron Transport Chain1.Transfer of electrons from NADH to coenzyme QNADH passes electrons via the NADH dehydrogenase complex (complex I) to FMN. The complex is also known as the NADH:CoQ oxidoreductase.NADH is produced by the α-ketoglutarate dehydrogenase, isocitrate dehydrogenase, and malate dehydrogenase reactions of the TCA cycle, by the pyruvate dehydrogenase reaction that converts pyruvate to acetyl-CoA, by β-oxidation of fatty acids, and by other oxidation reactions.NADH produced in the mitochondrial matrix diffuses to the inner mitochondrial membrane where it passes electrons to FMN, which is tightly bound to a protein.FMN passes the electrons through a series of iron–sulfur (Fe–S) complexes to coenzyme Q, which accepts electrons one at a time, forming first the semiquinone and then ubiquinol.The energy produced by these electron transfers is used to pump protons to the cytosolic side of the inner mitochondrial membrane.As the protons flow back into the matrix through the pores in the ATP synthase complex, ATP is generated.

8. 2. Transfer of electrons from coenzyme Q to cytochrome cCoenzyme Q passes electrons through Fe–S centers to cytochromes b and c1, which transfer the electrons to cytochrome c.The protein complex involved in these transfers is called complex III, or the cytochrome b-c1 complex. The complex is also known as CoQ:C1 oxidoreductase.These cytochromes each contain heme as a prosthetic group but have different apoproteins.In the ferric (Fe3+) state, the heme iron can accept one electron and be reduced to the ferrous (Fe2+) state.Because the cytochromes can only carry one electron at a time, two molecules in each cytochrome complex must be reduced for every molecule of NADH that is oxidized.The energy produced by the transfer of electrons from coenzyme Q to cytochrome c is used pump protons across the inner mitochondrial membrane.As the protons flow back into the matrix through the pores in the ATP synthase complex, ATP is generated.Electrons from FADH2, produced by reactions such as the oxidation of succinate to fumarate, enter the electron transport chain at complex II, which contains succinate dehydrogenase.Complex II will transfer electrons to coenzyme Q, without the associated proton pumping across the inner mitochondrial membrane.

9. 3.Transfer of electrons from cytochrome c to oxygenCytochrome c transfers electrons to the cytochrome aa3 complex, which transfers the electrons to molecular oxygen, reducing it to water.Cytochrome oxidase (complex IV) catalyzes this transfer of electrons.Cytochromes a and a3 each contain a heme and two different proteins that each contain copper.Two electrons are required to reduce one atom of oxygen; therefore, for each NADH that is oxidized, one-half of O2 is converted to H2O.The energy produced by the transfer of electrons from cytochrome c to oxygen is used to pump protons across the inner mitochondrial membrane.As the protons flow back into the matrix, ATP is generated.ATP Generation in ETCThe production of ATP is coupled to the transfer of electrons through the electron transport chain to O2. The overall process is known as oxidative phosphorylation. Protons flow down their electrochemical gradient through the membrane-bound ATP synthase. The flow of protons through the ATPase allows the enzyme to synthesize ATP.Significance of Electron Transport ChainThe electron transport chain is the final and most important step of cellular respiration.While Glycolysis and the Citric Acid Cycle make the necessary precursors, the electron transport chain is where a majority of the ATP is created.It has an important role in both cellular respiration.

10. ATP- Synthesis

11. Electron Transport Shuttles Inner mitochondrial membrane is impermeable to NADH of Glycolysis.NADH of Glycolysis can not deliverd electrons to ETS(Respiratory Chain) directly so,cells emply special reaction of transport the electrons to the ETS.This is called Shuttles and it is of two types –1- Malate –Asparate Shuttle-38 ATP Liver,Kidney,Heart cells 2- Glycerol-Phosphate Shuttle -36 ATP Skeletal and Brain cell

12. Electron Transport Shuttles

13. Referenceshttps://nurseslabs.com/respiratory-system/http://www.phschool.com/atschool/florida/pdfbooks/sci_Marieb/pdf/Marieb_ch22.pdfbio.libretexts.org/Bookshelves/Human_Biology/Book%3A_Human_Biology_(Wakim_and_Grewal)/16%3A_Respiratory_System/16.2%3A_Structure_and_Function_of_the_Respiratory_Systemhttps://westderbyschool.co.uk/userfiles/files/Curriculum/Revision%20Guides/PE/L3_Respiratory_System.pdfhttps://www.slideshare.net/mpattani/the-respiratory-system-60142115http://ncert.nic.in/NCERTS/l/kebo117.pdfhttps://quizlet.com/197913990/modified-respiratory-movements-flash-cards/A Textbook of Modern Zoology by Dr. Ramesh Guptahttps://media.lanecc.edu/users/driscolln/RT127/Softchalk/regulation_of_Breathing/https://ia803004.us.archive.org/31/items/akakkaakakakphyyyyssssiiiojajajaiiin/akakkaakakak%20Phyyyyssssiiio%20jajajaiiin.pdfhttps://www.unitypoint.org/homecare/article.aspx?id=2448b930-1451-43e4-8634-c0c16707c749https://en.wikipedia.org/wiki/Hering%E2%80%93Breuer_reflex

14. https://link.springer.com/referenceworkentry/10.1007%2F978-3-540-29678-2_4653https://opentextbc.ca/anatomyandphysiology/chapter/22-5-transport-of-gases/Jain JL, Jain S, and Jain N (2005). Fundamentals of Biochemistry. S. Chand and Company.Nelson DL and Cox MM. Lehninger Principles of Biochemistry. Fourth Edition.Berg JM et al. (2012) Biochemistry. Seventh Edition. W. H Freeman and Company.Berg JM, Tymoczko JL, Stryer L. Biochemistry. 5th edition. New York: W H Freeman; 2002. Section 17.2, Entry to the Citric Acid Cycle and Metabolism Through It Are Controlled. Available from: https://www.ncbi.nlm.nih.gov/books/NBK22347/https://en.wikipedia.org/wiki/Digestionhttps://www.news-medical.net/health/What-Does-the-Small-Intestine-Do.aspxhttps://biologydictionary.net/pharynx/Marieb, Elaine Nicpon,Hoehn, Katja. (2012) Human anatomy & physiology /Boston : Pearsonhttps://www.verywellhealth.com/what-are-digestive-enzymes-1945036https://socratic.org/questions/what-are-the-layers-of-the-gastrointestinal-tract-what-are-their-functionsA. K. Jain. Human Physiology book .Avichal Publishing Company,Delhihttps://www.ncbi.nlm.nih.gov/books/NBK537284/https://www.drbeen.com/blog/hormones-of-the-gastrointestinal-tract/H.R. Singh and Neeraj Kumar.Animal Physiology and Biochemistry.Vishal publishing Co.JalandharDr.V.K.Tyagi (2005)Animal Physiology and bio chemistry.Kedar nath Ram Nath ,Meerut.Dr. Ramesh Gupta..Modern Zoology a text book, Prakash Publication MuzaffnagarA.Guyton and J.E. Hall.(2010) Text book of Medical Physiologyhttps://google.comSmith, C. M., Marks, A. D., Lieberman, M. A., Marks, D. B., & Marks, D. B. (2005). Marks’ basic medical biochemistry: A clinical approach. Philadelphia: Lippincott Williams & Wilkins.Rodwell, V. W., Botham, K. M., Kennelly, P. J., Weil, P. A., & Bender, D. A. (2015). Harper’s illustrated biochemistry (30th ed.). New York, N.Y.: McGraw-Hill Education LLC.Lehninger, A. L., Nelson, D. L., & Cox, M. M. (2000). Lehninger principles of biochemistry. New York: Worth Publishers.Voet, D., & Voet, J. G. (1995). Biochemistry. New York: J. Wiley & Sons.