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Respiration as an energy
    transfer process




                           ALBIO9700/2006JK
Respiration
• A process in which organic molecules act as a
  fuel
• Molecules broken down to release chemical
  potential energy which is used to synthesise ATP
• Many cells can only use glucose as their
  respiratory substrate but others break down
  fatty acid, glycerol and amino acids in
  respiration
• Glucose breakdown occur in 4 stages:
  –   Glycolysis
  –   Link reaction
  –   Krebs cycle
  –   Oxidative phosphorylation
                                             ALBIO9700/2006JK
Glycolysis
• Splitting/lysis of glucose
• 6C glucose molecule to 2 molecules of 3C
  pyruvate
• ATP needed at first but energy released in
  later steps can be used to make ATP
• Net gain of 2 ATP molecules per glucose
  molecule broken down
• Takes place in cytoplasm
• Pyruvate enters link reaction in
  mitochondria
                                        ALBIO9700/2006JK
ALBIO9700/2006JK
Link reaction
• Pyruvate passed from cytoplasm into the
  mitochondrial matrix (active transport)
• Decarboxylated (CO2 removed), dehydrogenated
  and combined with coenzyme A (CoA) to give
  acetyl coenzyme A
• Coenzyme A:
   – adenine + ribose + pantothenic acid
   – acts as a carrier of acetyl groups to Krebs cycle
• Pyruvate + CoA + NAD ↔ acetyl CoA + CO2 + reduced NAD
• Fatty acids from fat metabolism also used to
  produce acetyl coenzyme A
                                                         ALBIO9700/2006JK
Krebs cycle
• aka citric acid cycle/tricarboxylic acid cycle
• Closed pathway of enzyme-controlled reactions:
  – Acetyl CoA + oxaloacetate (4C) → citrate (6C)
  – Citrate decarboxylated and dehydrogenated to yield
    CO2 (waste) and hydrogens (accepted by NAD and
    FAD)
  – Oxaloacetate is regenerated to combine with another
    acetyl CoA
• For each turn of the cycle, 2 CO2 produced, 1
  FAD and 3 NAD reduced and 1 ATP generated
• O2 not used
• Most important contribution: release of
  hydrogen (used in oxidative phosphorylation to
  provide energy to make ATP)
                                                  ALBIO9700/2006JK
ALBIO9700/2006JK
ALBIO9700/2006JK
Oxidative phosphorylation
• Energy for the phosphorylation of ADP to ATP
  comes from the activity of the electron transport
  chain (mitochondrial membranes)
• NADH and FADH2 are passed to the electron
  transport chain (ETC)
• Hydrogen      H+ and e-
• e- transferred to the first of a series of electron
  carriers; H+ remains in solution in mitochondrial
  matrix
• e- transferred to O2 (in solution), H+ drawn from
  solution to reduce O2 to H2O
• Transfer of e- along series of electron carriers
  makes energy available which is used to convert
  ADP + Pi to ATP
                                                ALBIO9700/2006JK
ALBIO9700/2006JK
• Potentially, 3 ATP from each NADH
  molecule/2 ATP from each FADH2
  molecule
• This yield cannot be realised unless ADP
  and Pi are available inside the
  mitochondrion
• 25% of total energy yield is used to
  transport ADP into the mitochondrion and
  ATP into cytoplasm
• Each NADH molecule entering the chain
  produces on average 2½ molecules of
  ATP and each FADH2 produces 1½
  molecules of ATP
                                       ALBIO9700/2006JK
ALBIO9700/2006JK
Sites of events of respiration in a cell




                                     ALBIO9700/2006JK
ALBIO9700/2006JK
Anaerobic respiration
• When free oxygen is not present, hydrogen
  cannot be disposed of by combination with
  oxygen
• ‘dumping’ hydrogen stops ETC and affects
  glycolysis
• 2 anaerobic pathways in cytoplasm which solve
  the problem:
  – Ethanol pathway (yeast and some plant tissues)
  – Lactate pathway (microorganisms and mammalian
    muscles)

                                              ALBIO9700/2006JK
• Ethanol pathway
  – Hydrogen from NADH is passed to ethanal (CH3CHO),
    releasing NAD and allows glycolysis to continue
  – Alcoholic fermentation: pyruvate decarboxylated
    to ethanal; ethanal reduced to ethanol (C2H5OH) by
    alcohol dehydrogenase
• Lactate pathway
  – Pyruvate acts as the hydrogen acceptor and is
    converted to lactate by lactate dehydrogenase
  – NAD is released and allows glycolysis to continue
• These reactions allow continued production of
  ATP even though oxygen is not available as the
  hydrogen acceptor

                                                    ALBIO9700/2006JK
• However, ethanol and lactate are toxic, and so
  reactions cannot continue indefinitely
• Pathway leading to ethanol cannot be reversed
  and the remaining chemical potential energy of
  ethanol is wasted
• Lactate pathway can be reversed in mammals
  (carried by blood plasma to the liver and
  converted back into pyruvate; 20% oxidised to
  CO2 and H2O via aerobic respiration when O2 is
  available again; remainder converted to
  glycogen)
• O2 needed to allow this removal of lactate is
  called oxygen debt
                                             ALBIO9700/2006JK
ALBIO9700/2006JK

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02 Respiration

  • 1. Respiration as an energy transfer process ALBIO9700/2006JK
  • 2. Respiration • A process in which organic molecules act as a fuel • Molecules broken down to release chemical potential energy which is used to synthesise ATP • Many cells can only use glucose as their respiratory substrate but others break down fatty acid, glycerol and amino acids in respiration • Glucose breakdown occur in 4 stages: – Glycolysis – Link reaction – Krebs cycle – Oxidative phosphorylation ALBIO9700/2006JK
  • 3. Glycolysis • Splitting/lysis of glucose • 6C glucose molecule to 2 molecules of 3C pyruvate • ATP needed at first but energy released in later steps can be used to make ATP • Net gain of 2 ATP molecules per glucose molecule broken down • Takes place in cytoplasm • Pyruvate enters link reaction in mitochondria ALBIO9700/2006JK
  • 5. Link reaction • Pyruvate passed from cytoplasm into the mitochondrial matrix (active transport) • Decarboxylated (CO2 removed), dehydrogenated and combined with coenzyme A (CoA) to give acetyl coenzyme A • Coenzyme A: – adenine + ribose + pantothenic acid – acts as a carrier of acetyl groups to Krebs cycle • Pyruvate + CoA + NAD ↔ acetyl CoA + CO2 + reduced NAD • Fatty acids from fat metabolism also used to produce acetyl coenzyme A ALBIO9700/2006JK
  • 6. Krebs cycle • aka citric acid cycle/tricarboxylic acid cycle • Closed pathway of enzyme-controlled reactions: – Acetyl CoA + oxaloacetate (4C) → citrate (6C) – Citrate decarboxylated and dehydrogenated to yield CO2 (waste) and hydrogens (accepted by NAD and FAD) – Oxaloacetate is regenerated to combine with another acetyl CoA • For each turn of the cycle, 2 CO2 produced, 1 FAD and 3 NAD reduced and 1 ATP generated • O2 not used • Most important contribution: release of hydrogen (used in oxidative phosphorylation to provide energy to make ATP) ALBIO9700/2006JK
  • 9. Oxidative phosphorylation • Energy for the phosphorylation of ADP to ATP comes from the activity of the electron transport chain (mitochondrial membranes) • NADH and FADH2 are passed to the electron transport chain (ETC) • Hydrogen H+ and e- • e- transferred to the first of a series of electron carriers; H+ remains in solution in mitochondrial matrix • e- transferred to O2 (in solution), H+ drawn from solution to reduce O2 to H2O • Transfer of e- along series of electron carriers makes energy available which is used to convert ADP + Pi to ATP ALBIO9700/2006JK
  • 11. • Potentially, 3 ATP from each NADH molecule/2 ATP from each FADH2 molecule • This yield cannot be realised unless ADP and Pi are available inside the mitochondrion • 25% of total energy yield is used to transport ADP into the mitochondrion and ATP into cytoplasm • Each NADH molecule entering the chain produces on average 2½ molecules of ATP and each FADH2 produces 1½ molecules of ATP ALBIO9700/2006JK
  • 13. Sites of events of respiration in a cell ALBIO9700/2006JK
  • 15. Anaerobic respiration • When free oxygen is not present, hydrogen cannot be disposed of by combination with oxygen • ‘dumping’ hydrogen stops ETC and affects glycolysis • 2 anaerobic pathways in cytoplasm which solve the problem: – Ethanol pathway (yeast and some plant tissues) – Lactate pathway (microorganisms and mammalian muscles) ALBIO9700/2006JK
  • 16. • Ethanol pathway – Hydrogen from NADH is passed to ethanal (CH3CHO), releasing NAD and allows glycolysis to continue – Alcoholic fermentation: pyruvate decarboxylated to ethanal; ethanal reduced to ethanol (C2H5OH) by alcohol dehydrogenase • Lactate pathway – Pyruvate acts as the hydrogen acceptor and is converted to lactate by lactate dehydrogenase – NAD is released and allows glycolysis to continue • These reactions allow continued production of ATP even though oxygen is not available as the hydrogen acceptor ALBIO9700/2006JK
  • 17. • However, ethanol and lactate are toxic, and so reactions cannot continue indefinitely • Pathway leading to ethanol cannot be reversed and the remaining chemical potential energy of ethanol is wasted • Lactate pathway can be reversed in mammals (carried by blood plasma to the liver and converted back into pyruvate; 20% oxidised to CO2 and H2O via aerobic respiration when O2 is available again; remainder converted to glycogen) • O2 needed to allow this removal of lactate is called oxygen debt ALBIO9700/2006JK