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Cell Respiration and Metabolism
Human
physiology
Metabolism
• All reactions that involve energy
transformations.
• Divided into 2 Categories:
▫ Catabolic:
 Release energy.
 Breakdown larger molecules into smaller
molecules.
▫ Anabolic:
 Require input of energy.
 Synthesis of large energy-storage molecules.
Aerobic Cell Respiration
• Oxidation-reduction reactions:
▫ Break down of molecules for energy.
▫ Electrons are transferred to
intermediate carriers, then to the final
electron acceptor: oxygen.
 Oxygen is obtained from the blood.
Glycolysis
• Breakdown of glucose for energy in the
cytoplasm.
• Glucose is converted to 2 molecules of pyruvic
acid (pyruvate).
• Each pyruvic acid contains:
▫ 3 carbons
▫ 3 oxygens
▫ 4 hydrogens
• 4 hydrogens are removed from intermediates.
Glycolysis
• Each pair of H+
reduces a molecule of NAD.
• Produces:
▫ 2 molecules of NADH and 2 unbound H+
▫ 2 ATP
• Glycolysis Pathway:
• Glucose + 2 NAD + 2 ADP + 2 Pi
2 pyruvic acid + 2 NADH and 2 ATP
Glycolysis
• Glycolysis is exergonic.
▫ Energy released used to drive endergonic reaction:
 ADP + Pi ATP
• Glucose must be activated first before energy
can be obtained.
▫ ATP consumed at the beginning of glycolysis.
Glycolysis
• ATP ADP + Pi
• Pi is not released but added to intermediate
molecules (phosphorylation).
• Phosphorylation of glucose, traps the glucose
inside the cell.
• Net gain of 2 ATP and 2 NADH.
Glycolysis
Lactic Acid Pathway
• Anaerobic respiration:
▫ Oxygen is not used in the process.
• NADH + H+
+ pyruvic acid
lactic acid and NAD.
• Produce 2 ATP/ glucose molecule.
Lactic Acid Pathway
• Some tissues adapted to anaerobic
metabolism:
▫ Skeletal muscle: normal daily
occurrence.
▫ RBCs do not contain mitochondria
and only use lactic acid pathway.
• Cardiac muscle: ischemia
Glycogenesis and
Glycogenolysis
• Increase glucose intracellularly,
would increase osmotic pressure.
• Must store carbohydrates in form
of glycogen.
• Glycogenesis: formation of glycogen from glucose.
• Glycogenolysis: conversion of glycogen to glucose-6-
phosphate.
▫ Glucose-6-phosphate can be utilized through glycolysis.
Glycogenesis and
Glycogenolysis
• Glucose-6-phosphate cannot leak out of the
cell.
• Skeletal muscles generate glucose-6-
phosphate for own glycolytic needs.
• Liver contains the enzyme glucose-6-
phosphatase that can remove the phosphate
group and produce free glucose.
Cori Cycle
• Lactic acid produced by anaerobic respiration
delivered to the liver.
• LDH converts lactic acid to pyruvic acid.
• Pyruvic acid converted to glucose-6-
phosphate:
▫ Intermediate for glycogen.
▫ Converted to free glucose.
• Gluconeogenesis: conversion to non-
carbohydrate molecules through pyruvic acid
to glucose.
Aerobic Respiration
• Aerobic respiration of glucose,
pyruvic acid is formed by
glycolysis, then converted into
acetyl coenzyme A (acetyl CoA).
• Energy is released in oxidative
reactions, and is captured as ATP.
Aerobic Respiration
• Pyruvic acid enters interior of
mitochondria.
• Converted to acetyl CoA and 2 C02.
• Acetyl CoA serves as substrate for
mitochondrial enzymes.
Acetyl CoA enters the Krebs Cycle.
overview
Krebs Cycle
• Acetyl CoA combines with oxaloacetic acid to
form citric acid.
• Citric acid enters the Krebs Cycle.
• Produces oxaloacetic acid to continue the
pathway.
• 1 GTP, 3 NADH, and 1 FADH2
• NADH and FADH2 transport electrons to
Electron Transport Cycle.
CAC
Electron Transport
• Cristae of inner mitochondrial
membrane contain molecules that
serve as electron transport system.
• Electron transport chain consists of
FMN, coenzyme Q, and cytochromes.
ETC Chain
• Each cytochrome transfers electron pairs from
NADH and FADH2 to next cytochrome.
• Oxidized NAD and FAD are regenerated and
shuttle electrons from the Krebs Cycle to the
ETC.
• Cytochrome receives a pair of electrons.
• Iron reduced, then oxidized as electrons are
transferred.
ETC Chain
• Cytochrome a3 transfers electrons to
O2 (final electron acceptor).
• Oxidative phosphorylation occurs:
▫ Energy derived is used to phosphorylate
ADP to ATP.
Coupling ETC to ATP
• Chemiosmotic theory:
• ETC powered by transport of
electrons, pumps H+
from
mitochondria matrix into space
between inner and outer
mitochondrial membranes.
Coupling ETC to ATP
• Proton pumps:
• NADH-coenzyme Q reductase complex:
▫ Transports 4 H+
for every pair of electrons.
• Cytochrome C reductase complex:
▫ Transports 4 H+
.
• Cytochrome C oxidase complex:
▫ Transports 2 H+
.
Coupling ETC to ATP
• Higher [H+
] in inter-membrane space.
• Respiratory assemblies:
▫ Permit the passage of H+
.
• Phosphorylation is coupled to oxidation, when
H+
diffuse through the respiratory assemblies:
▫ ADP and Pi ATP
Coupling ETC to ATP
• Oxygen functions as the last electron
acceptor.
▫ Oxidizes cytochrome a3.
• Oxygen accepts 2 electrons.
• O2 + 4 e-
+ 4 H+
2 H20
ATP Produced
• Direct phosphorylation:
• Glycolysis:
▫ 2 ATP
• Oxidative phosphorylation:
▫ 2.5 ATP produced for pair of electrons each
NADH donates.
▫ 1.5 ATP produced for each pair of electrons
FADH2 donates ((activates 2nd
and 3rd
proton
pumps).
▫ 26 ATP produced.
Metabolism of Lipids
• When more
energy is taken
in than
consumed,
glycolysis
inhibited.
• Glucose
converted into
glycogen and fat.
Lipogenesis
• Formation of
fat.
• Occurs mainly
in adipose
tissue and liver.
• Acetic acid
subunits from
acetyl CoA
converted into
various lipids.
Metabolism of Lipids
• Lipolysis:
▫ Breakdown of fat.
• Triglycerides glycerol + fa
• Free fatty acids (fa) serve as blood-
borne energy carriers.
lipase
Beta-oxidation
• Enzymes
remove
2-carbon
acetic acid
molecules
from acid end
of fa.
• Forms acetyl
CoA.
• Acetyl CoA
enters Krebs
Cycle.
Metabolism of Proteins
• Nitrogen is ingested primarily as protein.
• Excess nitrogen must be excreted.
• Nitrogen balance:
▫ Amount of nitrogen ingested minus amount
excreted.
• + N balance:
▫ Amount of nitrogen ingested more than amount excreted.
• - N balance:
▫ Amount of nitrogen excreted greater than ingested.
• Adequate amino acids are required for growth and repair. A
new amino acid can be obtained by:
• Transamination:
▫ Amino group (NH2) transferred from one amino acid to form another.
• Process by which excess amino acids are
eliminated.
• Amine group from glutamic acid removed, forming
ammonia and excreted as urea.
Deamination
• Energy
conversion:
amino acid is
deaminated.
• Ketoacid can
enter the Krebs
Cycle.
Use of different energy sources.

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Cell respiration and metabolism

  • 1. Cell Respiration and Metabolism Human physiology
  • 2. Metabolism • All reactions that involve energy transformations. • Divided into 2 Categories: ▫ Catabolic:  Release energy.  Breakdown larger molecules into smaller molecules. ▫ Anabolic:  Require input of energy.  Synthesis of large energy-storage molecules.
  • 3. Aerobic Cell Respiration • Oxidation-reduction reactions: ▫ Break down of molecules for energy. ▫ Electrons are transferred to intermediate carriers, then to the final electron acceptor: oxygen.  Oxygen is obtained from the blood.
  • 4. Glycolysis • Breakdown of glucose for energy in the cytoplasm. • Glucose is converted to 2 molecules of pyruvic acid (pyruvate). • Each pyruvic acid contains: ▫ 3 carbons ▫ 3 oxygens ▫ 4 hydrogens • 4 hydrogens are removed from intermediates.
  • 5.
  • 6. Glycolysis • Each pair of H+ reduces a molecule of NAD. • Produces: ▫ 2 molecules of NADH and 2 unbound H+ ▫ 2 ATP • Glycolysis Pathway: • Glucose + 2 NAD + 2 ADP + 2 Pi 2 pyruvic acid + 2 NADH and 2 ATP
  • 7. Glycolysis • Glycolysis is exergonic. ▫ Energy released used to drive endergonic reaction:  ADP + Pi ATP • Glucose must be activated first before energy can be obtained. ▫ ATP consumed at the beginning of glycolysis.
  • 8. Glycolysis • ATP ADP + Pi • Pi is not released but added to intermediate molecules (phosphorylation). • Phosphorylation of glucose, traps the glucose inside the cell. • Net gain of 2 ATP and 2 NADH.
  • 9.
  • 11. Lactic Acid Pathway • Anaerobic respiration: ▫ Oxygen is not used in the process. • NADH + H+ + pyruvic acid lactic acid and NAD. • Produce 2 ATP/ glucose molecule.
  • 12. Lactic Acid Pathway • Some tissues adapted to anaerobic metabolism: ▫ Skeletal muscle: normal daily occurrence. ▫ RBCs do not contain mitochondria and only use lactic acid pathway. • Cardiac muscle: ischemia
  • 13.
  • 14. Glycogenesis and Glycogenolysis • Increase glucose intracellularly, would increase osmotic pressure. • Must store carbohydrates in form of glycogen.
  • 15. • Glycogenesis: formation of glycogen from glucose. • Glycogenolysis: conversion of glycogen to glucose-6- phosphate. ▫ Glucose-6-phosphate can be utilized through glycolysis.
  • 16. Glycogenesis and Glycogenolysis • Glucose-6-phosphate cannot leak out of the cell. • Skeletal muscles generate glucose-6- phosphate for own glycolytic needs. • Liver contains the enzyme glucose-6- phosphatase that can remove the phosphate group and produce free glucose.
  • 17. Cori Cycle • Lactic acid produced by anaerobic respiration delivered to the liver. • LDH converts lactic acid to pyruvic acid. • Pyruvic acid converted to glucose-6- phosphate: ▫ Intermediate for glycogen. ▫ Converted to free glucose. • Gluconeogenesis: conversion to non- carbohydrate molecules through pyruvic acid to glucose.
  • 18.
  • 19. Aerobic Respiration • Aerobic respiration of glucose, pyruvic acid is formed by glycolysis, then converted into acetyl coenzyme A (acetyl CoA). • Energy is released in oxidative reactions, and is captured as ATP.
  • 20. Aerobic Respiration • Pyruvic acid enters interior of mitochondria. • Converted to acetyl CoA and 2 C02. • Acetyl CoA serves as substrate for mitochondrial enzymes.
  • 21. Acetyl CoA enters the Krebs Cycle.
  • 23. Krebs Cycle • Acetyl CoA combines with oxaloacetic acid to form citric acid. • Citric acid enters the Krebs Cycle. • Produces oxaloacetic acid to continue the pathway. • 1 GTP, 3 NADH, and 1 FADH2 • NADH and FADH2 transport electrons to Electron Transport Cycle.
  • 24. CAC
  • 25.
  • 26. Electron Transport • Cristae of inner mitochondrial membrane contain molecules that serve as electron transport system. • Electron transport chain consists of FMN, coenzyme Q, and cytochromes.
  • 27. ETC Chain • Each cytochrome transfers electron pairs from NADH and FADH2 to next cytochrome. • Oxidized NAD and FAD are regenerated and shuttle electrons from the Krebs Cycle to the ETC. • Cytochrome receives a pair of electrons. • Iron reduced, then oxidized as electrons are transferred.
  • 28. ETC Chain • Cytochrome a3 transfers electrons to O2 (final electron acceptor). • Oxidative phosphorylation occurs: ▫ Energy derived is used to phosphorylate ADP to ATP.
  • 29.
  • 30. Coupling ETC to ATP • Chemiosmotic theory: • ETC powered by transport of electrons, pumps H+ from mitochondria matrix into space between inner and outer mitochondrial membranes.
  • 31. Coupling ETC to ATP • Proton pumps: • NADH-coenzyme Q reductase complex: ▫ Transports 4 H+ for every pair of electrons. • Cytochrome C reductase complex: ▫ Transports 4 H+ . • Cytochrome C oxidase complex: ▫ Transports 2 H+ .
  • 32. Coupling ETC to ATP • Higher [H+ ] in inter-membrane space. • Respiratory assemblies: ▫ Permit the passage of H+ . • Phosphorylation is coupled to oxidation, when H+ diffuse through the respiratory assemblies: ▫ ADP and Pi ATP
  • 33. Coupling ETC to ATP • Oxygen functions as the last electron acceptor. ▫ Oxidizes cytochrome a3. • Oxygen accepts 2 electrons. • O2 + 4 e- + 4 H+ 2 H20
  • 34.
  • 35. ATP Produced • Direct phosphorylation: • Glycolysis: ▫ 2 ATP • Oxidative phosphorylation: ▫ 2.5 ATP produced for pair of electrons each NADH donates. ▫ 1.5 ATP produced for each pair of electrons FADH2 donates ((activates 2nd and 3rd proton pumps). ▫ 26 ATP produced.
  • 36. Metabolism of Lipids • When more energy is taken in than consumed, glycolysis inhibited. • Glucose converted into glycogen and fat.
  • 37. Lipogenesis • Formation of fat. • Occurs mainly in adipose tissue and liver. • Acetic acid subunits from acetyl CoA converted into various lipids.
  • 38. Metabolism of Lipids • Lipolysis: ▫ Breakdown of fat. • Triglycerides glycerol + fa • Free fatty acids (fa) serve as blood- borne energy carriers. lipase
  • 39. Beta-oxidation • Enzymes remove 2-carbon acetic acid molecules from acid end of fa. • Forms acetyl CoA. • Acetyl CoA enters Krebs Cycle.
  • 40. Metabolism of Proteins • Nitrogen is ingested primarily as protein. • Excess nitrogen must be excreted. • Nitrogen balance: ▫ Amount of nitrogen ingested minus amount excreted. • + N balance: ▫ Amount of nitrogen ingested more than amount excreted. • - N balance: ▫ Amount of nitrogen excreted greater than ingested.
  • 41. • Adequate amino acids are required for growth and repair. A new amino acid can be obtained by: • Transamination: ▫ Amino group (NH2) transferred from one amino acid to form another.
  • 42. • Process by which excess amino acids are eliminated. • Amine group from glutamic acid removed, forming ammonia and excreted as urea.
  • 43. Deamination • Energy conversion: amino acid is deaminated. • Ketoacid can enter the Krebs Cycle.
  • 44. Use of different energy sources.