Cellular respiration
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Transcript Cellular respiration
METABOLISM
26-1
Functions of food
source of energy
essential nutrients
stored for future use
Metabolism is all the chemical reactions of the
body
some reactions produce the energy which is
stored in ATP that other reactions consume
all molecules will eventually be broken down
and recycled or excreted from the body
CATABOLISM AND ANABOLISM
26-2
Catabolic reactions breakdown complex organic
compounds
providing energy (exergonic)
glycolysis, Krebs cycle and electron transport
Anabolic reactions synthesize complex
molecules from small molecules
requiring energy (endergonic)
Exchange of energy requires use of ATP
(adenosine triphosphate) molecule.
ATP MOLECULE & ENERGY
Each cell has about 1 billion ATP molecules that last for less
than one minute
Over half of the energy released from ATP is converted to heat
26-3
ENERGY TRANSFER
Energy is found in the bonds between atoms
Oxidation is a decrease in the energy
content of a molecule
Reduction is the increase in the energy
content of a molecule
Oxidation-reduction reactions are always
coupled within the body
26-4
whenever a substance is oxidized, another is
almost simultaneously reduced.
OXIDATION AND REDUCTION
Biological oxidation involves the loss of electron
and a proton (hydrogen atom)
dehydrogenation reactions require coenzymes
to transfer hydrogen atoms to another
compound
common coenzymes of living cells that carry H+
26-5
NAD (nicotinamide adenine dinucleotide )
NADP (nicotinamide adenine dinucleotide phosphate )
FAD (flavin adenine dinucleotide )
NAD+ + 2 H NADH + H+
Biological reduction is the addition of electron and
a proton (hydrogen atom) to a molecule
increase in potential energy of the molecule
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CARBOHYDRATE METABOLISM
Dietary carbohydrate burned as fuel within
hours of absorption
All oxidative carbohydrate consumption is
essentially a matter of glucose catabolism
C6H12O6 + 6O2 6CO2 + 6H2O+ energy
Function of this reaction is to transfers energy
from glucose to ATP
not
to produce carbon dioxide and water
26-7
GLUCOSE CATABOLISM
Glucose catabolism – a series of small steps, each controlled
by a separate enzyme, in which energy is released in small
manageable amounts, and as much as possible, is transferred
to ATP and the rest is released as heat
Three major pathways of glucose catabolism
glycolysis
glucose (6C) split into 2 pyruvic acid molecules (3C)
anaerobic
fermentation
occurs in the absence of oxygen
reduces pyruvic acid to lactic acid
aerobic
respiration
occurs in the presence of oxygen
completely oxidizes pyruvic acid to CO2 and H2O
26-8
MECHANISMS OF ATP GENERATION
Phosphorylation is
bond attaching 3rd phosphate
group contains stored energy
Mechanisms of phosphorylation
within animals
substrate-level phosphorylation in cytosol
oxidative phosphorylation in mitochondria
in
chlorophyll-containing plants
or bacteria
photophosphorylation.
26-9
OVERVIEW OF ATP PRODUCTION
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Key
Carbon atoms
Glucose
ATP
Phosphate
groups
1 Phosphorylation
ADP
Glucose 6-phosphate
Glycogen
Fat
Fructose 6-phosphate
ATP
2 Priming
ADP
Fructose 1,6-diphosphate
3 Cleavage
2 PGAL
2 Pi
2 NAD+
2 NADH + 2 H+
4 Oxidation
2
2 ADP
2 H2O
2 ATP
2
5 Dephosphorylation
2 ADP
2 ATP
2
2 pyruvic acid
2 NADH + 2 H+
2 NAD+
2
2 lactic acid
Anaerobic fermentation
Aerobic respiration
26-10
STEPS OF GLYCOLYSIS (1)
Phosphorylation
Priming
glucose enters cell has
phosphate added - ATP used
maintains favorable
concentration gradient,
prevents glucose from leaving
cell
isomerization occurs
phosphorylation further
activates molecule - ATP used
Cleavage
molecule split into 2 threecarbon molecules
26-11
STEPS OF GLYCOLYSIS (2)
Oxidation
removes H+
NAD+ + H NADH
Dephosphorylation
transfers phosphate
groups to ADP to form ATP
4 ATPs produced (2 ATP
used) for a net gain of 2
ATP
produces 2 pyruvic acid
Animation
26-12
STEPS OF GLYCOLYSIS
4 ATP are produced but 2 ATP were consumed to
initiate glycolysis, so net gain is 2 ATP per glucose
molecule
Some energy originally in the glucose is contained in
the ATP, some in the NADH, some is lost as heat, but
most of the energy remains in the pyruvic acid
End-products of glycolysis are:
2 pyruvic acid + 2 NADH + 2 ATP
26-13
ANAEROBIC FERMENTATION
Fate of pyruvic acid depends on oxygen
availability
In an exercising muscle, demand for ATP > oxygen
supply; ATP produced by glycolysis
Lactic acid travels to liver to be oxidized back to
pyruvic when O2 is available (oxygen debt)
glycolysis can not continue without supply of NAD+
NADH reduces pyruvic acid to lactic acid, restoring NAD+
then stored as glycogen or released as glucose
Fermentation is inefficient, not favored by brain or
heart
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ANAEROBIC FERMENTATION
Lactic acid leaves the cells that generate it
Liver can also convert lactic acid back to G6P and can:
polymerize it to form glycogen for storage
remove phosphate group and release free glucose into the blood
Drawbacks of anaerobic fermentation
enter bloodstream and transported to the liver
when oxygen becomes available the liver oxidized it back to pyruvic
acid
oxygen is part of the oxygen debt created by exercising muscle
wasteful, because most of the energy of glucose is still in the lactic
acid and has contributed no useful work
lactic acid is toxic and contributes to muscle fatigue
Skeletal muscle is relatively tolerant of anaerobic
fermentation, cardiac muscle less so
the brain employs no anaerobic fermentation
26-15
AEROBIC RESPIRATION
Most ATP generated in mitochondria, which requires
oxygen as final electron acceptor
In the presence of oxygen, pyruvic acid enters the
mitochondria and is oxidized by aerobic respiration
Occurs in two principal steps:
matrix reactions – their controlling enzymes are in
the fluid of the mitochondrial matrix
membrane reactions - whose controlling enzymes
are bound to the membranes of the mitochondrial
cristae
26-16
MITOCHONDRIAL MATRIX REACTIONS
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Pyruvic acid (C3)
6
CO2
Pyruvic acid oxidation
NAD+
7
NADH + H+
Acetyl group (C2)
8
Acetyl-Co A
Coenzyme A
H2O
9
Citric acid (C6)
Oxaloacetic acid (C4)
H2O
10
NADH + H+
NAD+
(C6)
Citric
acid
cycle
18
H2O
NAD+
11
Citric acid (Krebs) Cycle
NADH + H+
(C4)
12
CO2
17
(C5)
H2O
13
Occurs in
mitochondrial
matrix
(C4)
NADH + H+
14
16
FADH2
NAD+
(C4)
CO2
FAD
(C4)
Pi
15
GTP
GDP
26-17
ADP
ATP
MITOCHONDRIAL MATRIX REACTIONS
Three steps prepare pyruvic acid
to enter citric acid cycle
decarboxylation so that a 3-carbon
compound becomes a 2-carbon
compound
convert that to an acetyl group
(acetic acid)
CO2 removed from pyruvic acid
NAD+ removes hydrogen atoms from
the C2 compound
acetyl group binds to coenzyme A
results in acetyl-coenzyme A (acetylCoA)
26-18
MITOCHONDRIAL MATRIX REACTIONS
Citric Acid Cycle
acetyl-Co A (a C2 compound) combines
with a C4 to form a C6 compound (citric
acid)-- start of cycle
hydrogen atoms are removed and
accepted by NAD+
another CO2 is removed and the substrate
becomes a five-carbon chain
previous step repeated removing another
free CO2 leaving a four-carbon chain
ATP
two hydrogen atoms are removed and
accepted by the coenzyme FAD
two final hydrogen atoms are removed and
transferred to NAD+
reaction generates oxaloacetic acid, which
starts the cycle again
26-19
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SUMMARY OF MATRIX REACTIONS
2 pyruvate + 6H2O 6CO2
2 ADP + 2 Pi 2 ATP
8 NAD+ + 8 H2 8 NADH + 8 H+
2 FAD + 2 H2 2 FADH2
Carbon atoms of glucose have all been carried away as CO2 and
exhaled
Energy lost as heat, stored in 2 ATP, 8 reduced NADH, 2 FADH2
molecules of the matrix reactions and 2 NADH from glycolysis
Citric acid cycle is a source of substances for synthesis of fats
and nonessential amino acids
26-21
MEMBRANE REACTIONS
Membrane reactions have two
purposes:
to further oxidize NADH and FADH2
and transfer their energy to ATP
to regenerate NAD+ and FAD and
make them available again to earlier
reaction steps
Mitochondrial electron-transport chain
– series of compounds that carry out
this series of membrane reactions
most bound to the inner
mitochondrial membrane
arranged in a precise order that
enables each one to receive a pair of
electrons from the member on the
left side of it.
pass electrons to member on the
other side
26-22
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ELECTRON TRANSPORT CHAIN
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50
NADH + H+
NAD+
FMN
Relative free energy (kcal/mole)
Fe-S
40
FADH2
Enzyme complex 1
FAD
CoQ
30
Figure 26.5
Cyt b
Fe-S
Cyt c1
20
Enzyme complex 2
Cyt c
Cu
10
Cyt a
Cyt a3
Enzyme complex 3
½ O2 + 2 H+
H2O
0
Reaction progress
26-24
CHEMIOSMOTIC MECHANISM
Electron transport chain energy fuels respiratory
enzyme complexes
pump protons from matrix into space between
inner and outer mitochondrial membranes
creates steep electrochemical gradient for H+
across inner mitochondrial membrane
Inner membrane is permeable to H+ at channel
proteins called ATP synthase
Chemiosmotic mechanism - H+ current rushing back
through these ATP synthase channels drives ATP
synthesis (ANIMATION)
26-25
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OVERVIEW OF ATP PRODUCTION
NADH releases an electron pair to electron
transport system and H+ to prime pumps
enough
FADH2 releases its electron pairs further along
electron-transport system
enough
energy to synthesize 3 ATP
energy to synthesize 2 ATP
Complete aerobic oxidation of glucose to CO2
and H2O produces 36-38 ATP
efficiency
rating of 40% - 60% is lost as heat
26-27
26-28
ATP GENERATED BY OXIDATION OF GLUCOSE
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Glucose
2 ATP
Glycolysis
(net)
2 NADH + 2 H+
Cytosol
2 pyruvate
Mitochondria
2 NADH + 2 H+
CO2
6 NADH + 6 H+
Citric acid
cycle
2 ATP
2 FADH2
Electron-transport
chain
O2
H2O
4 ATP
28–30
ATP
Total 36–38
ATP
26-29
GLYCOGEN METABOLISM
ATP is quickly used after it is formed
Glycogenesis - synthesis of glycogen
stimulated by insulin
chains glucose monomers together
Glycogenolysis – hydrolysis of glycogen
it is an energy transfer molecule, not an energy storage molecule
converts the extra glucose to other compounds better suited for energy
storage (glycogen and fat)
releases glucose between meals
stimulated by glucagon and epinephrine
only liver cells can release glucose back into blood
Gluconeogenesis - synthesis of glucose from
noncarbohydrates, such as glycerol and amino acids
occurs chiefly in the liver and later, kidneys if necessary
26-30
GLUCOSE STORAGE AND USE
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Blood
glucose
Extracellular
Intracellular
Glucose
6-phosphatase
(in liver, kidney,
and intestinal cells)
Hexokinase
(in all cells)
Glucose 6-phosphate
Glycogen
synthase
Key
Pi
Glucose
1-phosphate
Glycogenesis
Glycogenolysis
Glycogen
phosphorylase
Glycogen
Pi
Glycolysis
Figure 26.8
26-31
LIPIDS
Triglycerides are stored in body’s adipocytes
constant
turnover of lipid molecules every 2 - 3
weeks
released
into blood, transported and either oxidized or
redeposited in other fat cells
Lipogenesis - synthesis of fat from other types
of molecules
amino
acids and sugars used to make fatty acids
and glycerol
PGAL can be converted to glycerol
26-32
LIPIDS
Lipolysis – breaking down fat for fuel
begins with the hydrolysis of a triglyceride to glycerol
and fatty acids
stimulated by epinephrine, norepinephrine,
glucocorticoids, thyroid hormone, and growth
hormone
glycerol easily converted to PGAL and enters the
pathway of glycolysis
beta oxidation in the mitochondrial matrix catabolizes
the fatty acid components
generates only half as much ATP as glucose
removes two carbon atoms at a time which bonds to coenzyme A
forms acetyl-CoA, the entry point for the citric acid cycle
a fatty acid with 16 carbons can yield 129 molecules
of ATP
richer source of energy than the glucose molecule
26-33
LIPOGENESIS AND LIPOLYSIS PATHWAYS
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Glucose
Glucose 6-phosphate
Stored
triglycerides
Glycerol
PGAL
Fatty acids
Glycerol
Beta oxidation
Pyruvic
acid
Fatty
acids
Acetyl groups
New
triglycerides
Acetyl-Co A
Ketone bodies
β-hydroxybutyric acid
Acetoacetic acid
Acetone
Citric
acid
cycle
Key
Lipogenesis
Lipolysis
26-34
KETOGENESIS
Fatty acids catabolized into acetyl groups (by
beta-oxidation in mitochondrial matrix) may:
enter
citric acid cycle as acetyl-CoA
undergo ketogenesis
metabolized
by liver to produce ketone bodies
acetoacetic acid
-hydroxybutyric acid
acetone
rapid
or incomplete oxidization of fats raises blood
ketone levels (ketosis) and may lead to a pH imbalance
(ketoacidosis)
26-35
PROTEINS
Amino acids in the pool can be converted to others
Free amino acids also can be converted to glucose and fat or
directly used as fuel
Conversions involve three processes:
deamination – removal of an amino group (-NH2)
amination – addition of -NH2
transamination – transfer of -NH2 from one molecule to another
As fuel - first must be deaminated (removal of -NH2)
what remains is keto acid and may be converted to pyruvic acid,
acetyl-CoA, or one of the acids of the citric acid cycle
during shortage of amino acids, citric acid cycle intermediates can be
aminated and converted to amino acids
in gluconeogenesis, keto acids are used to synthesis glucose
26-36