AP Biology Chapter 9
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Transcript of AP Biology Chapter 9
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Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
PowerPoint® Lecture Presentations for
Biology Eighth Edition
Neil Campbell and Jane Reece
Lectures by Chris Romero, updated by Erin Barley with contributions from Joan Sharp
Chapter 9Chapter 9
Cellular Respiration: Harvesting Chemical Energy
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Overview: Life Is Work
• Living cells require energy from outside sources
• Some animals, such as the giant panda, obtain energy by eating plants, and some animals feed on other organisms that eat plants
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Fig. 9-1
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• Energy flows into an ecosystem as sunlight and leaves as heat
• Photosynthesis generates O2 and organic molecules, which are used in cellular respiration
• Cells use chemical energy stored in organic molecules to regenerate ATP, which powers work
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Fig. 9-2
Lightenergy
ECOSYSTEM
Photosynthesis in chloroplasts
CO2 + H2O
Cellular respirationin mitochondria
Organicmolecules+ O2
ATP powers most cellular work
Heatenergy
ATP
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Concept 9.1: Catabolic pathways yield energy by oxidizing organic fuels
• Several processes are central to cellular respiration and related pathways
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Catabolic Pathways and Production of ATP
• The breakdown of organic molecules is exergonic
• Fermentation is a partial degradation of sugars that occurs without O2
• Aerobic respiration consumes organic molecules and O2 and yields ATP
• Anaerobic respiration is similar to aerobic respiration but consumes compounds other than O2
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• Cellular respiration includes both aerobic and anaerobic respiration but is often used to refer to aerobic respiration
• Although carbohydrates, fats, and proteins are all consumed as fuel, it is helpful to trace cellular respiration with the sugar glucose:
C6H12O6 + 6 O2 6 CO2 + 6 H2O + Energy (ATP + heat)
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Redox Reactions: Oxidation and Reduction
• The transfer of electrons during chemical reactions releases energy stored in organic molecules
• This released energy is ultimately used to synthesize ATP
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The Principle of Redox
• Chemical reactions that transfer electrons between reactants are called oxidation-reduction reactions, or redox reactions
• In oxidation, a substance loses electrons, or is oxidized
• In reduction, a substance gains electrons, or is reduced (the amount of positive charge is reduced)
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Fig. 9-UN1
becomes oxidized(loses electron)
becomes reduced(gains electron)
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Fig. 9-UN2
becomes oxidized
becomes reduced
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• The electron donor is called the reducing agent
• The electron receptor is called the oxidizing agent
• Some redox reactions do not transfer electrons but change the electron sharing in covalent bonds
• An example is the reaction between methane and O2
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Fig. 9-3
Reactants
becomes oxidized
becomes reduced
Products
Methane(reducing
agent)
Oxygen(oxidizing
agent)
Carbon dioxide Water
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Oxidation of Organic Fuel Molecules During Cellular Respiration
• During cellular respiration, the fuel (such as glucose) is oxidized, and O2 is reduced:
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Fig. 9-UN3
becomes oxidized
becomes reduced
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Fig. 9-UN4
Dehydrogenase
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Stepwise Energy Harvest via NAD+ and the Electron Transport Chain
• In cellular respiration, glucose and other organic molecules are broken down in a series of steps
• Electrons from organic compounds are usually first transferred to NAD+, a coenzyme
• As an electron acceptor, NAD+ functions as an oxidizing agent during cellular respiration
• Each NADH (the reduced form of NAD+) represents stored energy that is tapped to synthesize ATP
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Fig. 9-4
Dehydrogenase
Reduction of NAD+
Oxidation of NADH
2 e– + 2 H+
2 e– + H+
NAD+ + 2[H]
NADH
+
H+
H+
Nicotinamide(oxidized form)
Nicotinamide(reduced form)
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• NADH passes the electrons to the electron transport chain
• Unlike an uncontrolled reaction, the electron transport chain passes electrons in a series of steps instead of one explosive reaction
• O2 pulls electrons down the chain in an energy-yielding tumble
• The energy yielded is used to regenerate ATP
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Fig. 9-5
Fre
e en
erg
y, G
Fre
e en
erg
y, G
(a) Uncontrolled reaction
H2O
H2 + 1/2 O2
Explosiverelease of
heat and lightenergy
(b) Cellular respiration
Controlledrelease ofenergy for
synthesis ofATP
2 H+ + 2 e–
2 H + 1/2 O2
(from food via NADH)
ATP
ATP
ATP
1/2 O22 H+
2 e–E
lectron
transp
ort
chain
H2O
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The Stages of Cellular Respiration: A Preview
• Cellular respiration has three stages:
– Glycolysis (breaks down glucose into two molecules of pyruvate)
– The citric acid cycle (completes the breakdown of glucose)
– Oxidative phosphorylation (accounts for most of the ATP synthesis)
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Fig. 9-6-1
Substrate-levelphosphorylation
ATP
Cytosol
Glucose Pyruvate
Glycolysis
Electronscarried
via NADH
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Fig. 9-6-2
Mitochondrion
Substrate-levelphosphorylation
ATP
Cytosol
Glucose Pyruvate
Glycolysis
Electronscarried
via NADH
Substrate-levelphosphorylation
ATP
Electrons carriedvia NADH and
FADH2
Citricacidcycle
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Fig. 9-6-3
Mitochondrion
Substrate-levelphosphorylation
ATP
Cytosol
Glucose Pyruvate
Glycolysis
Electronscarried
via NADH
Substrate-levelphosphorylation
ATP
Electrons carriedvia NADH and
FADH2
Oxidativephosphorylation
ATP
Citricacidcycle
Oxidativephosphorylation:electron transport
andchemiosmosis
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• The process that generates most of the ATP is called oxidative phosphorylation because it is powered by redox reactions
BioFlix: Cellular RespirationBioFlix: Cellular Respiration
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• Oxidative phosphorylation accounts for almost 90% of the ATP generated by cellular respiration
• A smaller amount of ATP is formed in glycolysis and the citric acid cycle by substrate-level phosphorylation
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Fig. 9-7
Enzyme
ADP
PSubstrate
Enzyme
ATP+
Product
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Concept 9.2: Glycolysis harvests chemical energy by oxidizing glucose to pyruvate
• Glycolysis (“splitting of sugar”) breaks down glucose into two molecules of pyruvate
• Glycolysis occurs in the cytoplasm and has two major phases:
– Energy investment phase
– Energy payoff phase
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Fig. 9-8
Energy investment phase
Glucose
2 ADP + 2 P 2 ATP used
formed4 ATP
Energy payoff phase
4 ADP + 4 P
2 NAD+ + 4 e– + 4 H+ 2 NADH + 2 H+
2 Pyruvate + 2 H2O
2 Pyruvate + 2 H2OGlucoseNet
4 ATP formed – 2 ATP used 2 ATP
2 NAD+ + 4 e– + 4 H+ 2 NADH + 2 H+
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Fig. 9-9-1
ATP
ADP
Hexokinase1
ATP
ADP
Hexokinase1
Glucose
Glucose-6-phosphate
Glucose
Glucose-6-phosphate
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Fig. 9-9-2
Hexokinase
ATP
ADP
1
Phosphoglucoisomerase2
Phosphogluco-isomerase
2
Glucose
Glucose-6-phosphate
Fructose-6-phosphate
Glucose-6-phosphate
Fructose-6-phosphate
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1
Fig. 9-9-3
Hexokinase
ATP
ADP
Phosphoglucoisomerase
Phosphofructokinase
ATP
ADP
2
3
ATP
ADP
Phosphofructo-kinase
Fructose-1, 6-bisphosphate
Glucose
Glucose-6-phosphate
Fructose-6-phosphate
Fructose-1, 6-bisphosphate
1
2
3
Fructose-6-phosphate
3
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Fig. 9-9-4
Glucose
ATP
ADP
Hexokinase
Glucose-6-phosphate
Phosphoglucoisomerase
Fructose-6-phosphate
ATP
ADP
Phosphofructokinase
Fructose-1, 6-bisphosphate
Aldolase
Isomerase
Dihydroxyacetonephosphate
Glyceraldehyde-3-phosphate
1
2
3
4
5
Aldolase
Isomerase
Fructose-1, 6-bisphosphate
Dihydroxyacetonephosphate
Glyceraldehyde-3-phosphate
4
5
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Fig. 9-9-52 NAD+
NADH2
+ 2 H+
2
2 P i
Triose phosphatedehydrogenase
1, 3-Bisphosphoglycerate
6
2 NAD+
Glyceraldehyde-3-phosphate
Triose phosphatedehydrogenase
NADH2
+ 2 H+
2 P i
1, 3-Bisphosphoglycerate
6
2
2
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Fig. 9-9-62 NAD+
NADH2
Triose phosphatedehydrogenase
+ 2 H+
2 P i
2
2 ADP
1, 3-Bisphosphoglycerate
Phosphoglycerokinase2 ATP
2 3-Phosphoglycerate
6
7
2
2 ADP
2 ATP
1, 3-Bisphosphoglycerate
3-Phosphoglycerate
Phosphoglycero-kinase
2
7
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Fig. 9-9-7
3-Phosphoglycerate
Triose phosphatedehydrogenase
2 NAD+
2 NADH+ 2 H+
2 P i
2
2 ADP
Phosphoglycerokinase
1, 3-Bisphosphoglycerate
2 ATP
3-Phosphoglycerate2
Phosphoglyceromutase
2-Phosphoglycerate2
2-Phosphoglycerate2
2
Phosphoglycero-mutase
6
7
8
8
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Fig. 9-9-82 NAD+
NADH2
2
2
2
2
+ 2 H+
Triose phosphatedehydrogenase2 P i
1, 3-Bisphosphoglycerate
Phosphoglycerokinase
2 ADP
2 ATP
3-Phosphoglycerate
Phosphoglyceromutase
Enolase
2-Phosphoglycerate
2 H2O
Phosphoenolpyruvate
9
8
7
6
2 2-Phosphoglycerate
Enolase
2
2 H2O
Phosphoenolpyruvate
9
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Fig. 9-9-9
Triose phosphatedehydrogenase
2 NAD+
NADH2
2
2
2
2
2
2 ADP
2 ATP
Pyruvate
Pyruvate kinase
Phosphoenolpyruvate
Enolase2 H2O
2-Phosphoglycerate
Phosphoglyceromutase
3-Phosphoglycerate
Phosphoglycerokinase
2 ATP
2 ADP
1, 3-Bisphosphoglycerate
+ 2 H+
6
7
8
9
10
2
2 ADP
2 ATP
Phosphoenolpyruvate
Pyruvate kinase
2 Pyruvate
10
2 P i
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Concept 9.3: The citric acid cycle completes the energy-yielding oxidation of organic molecules
• In the presence of O2, pyruvate enters the mitochondrion
• Before the citric acid cycle can begin, pyruvate must be converted to acetyl CoA, which links the cycle to glycolysis
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Fig. 9-10
CYTOSOL MITOCHONDRION
NAD+ NADH + H+
2
1 3
Pyruvate
Transport protein
CO2Coenzyme A
Acetyl CoA
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• The citric acid cycle, also called the Krebs cycle, takes place within the mitochondrial matrix
• The cycle oxidizes organic fuel derived from pyruvate, generating 1 ATP, 3 NADH, and 1 FADH2 per turn
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Fig. 9-11
Pyruvate
NAD+
NADH
+ H+Acetyl CoA
CO2
CoA
CoA
CoA
Citricacidcycle
FADH2
FAD
CO22
3
3 NAD+
+ 3 H+
ADP + P i
ATP
NADH
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• The citric acid cycle has eight steps, each catalyzed by a specific enzyme
• The acetyl group of acetyl CoA joins the cycle by combining with oxaloacetate, forming citrate
• The next seven steps decompose the citrate back to oxaloacetate, making the process a cycle
• The NADH and FADH2 produced by the cycle relay electrons extracted from food to the electron transport chain
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Fig. 9-12-1
Acetyl CoA
Oxaloacetate
CoA—SH
1
Citrate
Citricacidcycle
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Fig. 9-12-2
Acetyl CoA
Oxaloacetate
Citrate
CoA—SH
Citricacidcycle
1
2
H2O
Isocitrate
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Fig. 9-12-3
Acetyl CoA
CoA—SH
Oxaloacetate
Citrate
H2O
Citricacidcycle
Isocitrate
1
2
3
NAD+
NADH
+ H+
-Keto-glutarate
CO2
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Fig. 9-12-4
Acetyl CoA
CoA—SH
Oxaloacetate
Citrate
H2O
IsocitrateNAD+
NADH
+ H+
Citricacidcycle
-Keto-glutarate
CoA—SH
1
2
3
4
NAD+
NADH
+ H+SuccinylCoA
CO2
CO2
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Fig. 9-12-5
Acetyl CoA
CoA—SH
Oxaloacetate
Citrate
H2O
IsocitrateNAD+
NADH
+ H+
CO2
Citricacidcycle
CoA—SH -Keto-
glutarate
CO2NAD+
NADH
+ H+SuccinylCoA
1
2
3
4
5
CoA—SH
GTP GDP
ADP
P iSuccinate
ATP
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Fig. 9-12-6
Acetyl CoA
CoA—SH
Oxaloacetate
H2O
CitrateIsocitrate
NAD+
NADH
+ H+
CO2
Citricacidcycle
CoA—SH -Keto-
glutarate
CO2NAD+
NADH
+ H+
CoA—SH
P
SuccinylCoA
i
GTP GDP
ADP
ATP
Succinate
FAD
FADH2
Fumarate
1
2
3
4
5
6
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Fig. 9-12-7
Acetyl CoA
CoA—SH
Oxaloacetate
Citrate
H2O
IsocitrateNAD+
NADH
+ H+
CO2
-Keto-glutarate
CoA—SH
NAD+
NADH
SuccinylCoA
CoA—SH
PP
GDPGTP
ADP
ATP
Succinate
FAD
FADH2
Fumarate
CitricacidcycleH2O
Malate
1
2
5
6
7
i
CO2
+ H+
3
4
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Fig. 9-12-8
Acetyl CoA
CoA—SH
Citrate
H2O
IsocitrateNAD+
NADH
+ H+
CO2
-Keto-glutarate
CoA—SH
CO2NAD+
NADH
+ H+SuccinylCoA
CoA—SH
P i
GTP GDP
ADP
ATP
Succinate
FAD
FADH2
Fumarate
CitricacidcycleH2O
Malate
Oxaloacetate
NADH
+H+
NAD+
1
2
3
4
5
6
7
8
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Concept 9.4: During oxidative phosphorylation, chemiosmosis couples electron transport to ATP synthesis
• Following glycolysis and the citric acid cycle, NADH and FADH2 account for most of the energy extracted from food
• These two electron carriers donate electrons to the electron transport chain, which powers ATP synthesis via oxidative phosphorylation
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The Pathway of Electron Transport
• The electron transport chain is in the cristae of the mitochondrion
• Most of the chain’s components are proteins, which exist in multiprotein complexes
• The carriers alternate reduced and oxidized states as they accept and donate electrons
• Electrons drop in free energy as they go down the chain and are finally passed to O2, forming H2O
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Fig. 9-13
NADH
NAD+2FADH2
2 FADMultiproteincomplexesFAD
Fe•S
FMN
Fe•S
Q
Fe•S
Cyt b
Cyt c1
Cyt c
Cyt a
Cyt a3
IV
Fre
e en
erg
y (G
) r e
lat i
ve t
o O
2 (
kcal
/mo
l)
50
40
30
20
10 2
(from NADHor FADH2)
0 2 H+ + 1/2 O2
H2O
e–
e–
e–
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• Electrons are transferred from NADH or FADH2 to the electron transport chain
• Electrons are passed through a number of proteins including cytochromes (each with an iron atom) to O2
• The electron transport chain generates no ATP
• The chain’s function is to break the large free-energy drop from food to O2 into smaller steps that release energy in manageable amounts
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Chemiosmosis: The Energy-Coupling Mechanism
• Electron transfer in the electron transport chain causes proteins to pump H+ from the mitochondrial matrix to the intermembrane space
• H+ then moves back across the membrane, passing through channels in ATP synthase
• ATP synthase uses the exergonic flow of H+ to drive phosphorylation of ATP
• This is an example of chemiosmosis, the use of energy in a H+ gradient to drive cellular work
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Fig. 9-14
INTERMEMBRANE SPACE
Rotor
H+
Stator
Internalrod
Cata-lyticknob
ADP+P ATP
i
MITOCHONDRIAL MATRIX
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Fig. 9-15EXPERIMENT
Electromagnet
RESULTS
Sample
Magnetic bead
Internalrod
Catalyticknob
Nickelplate
Rotation in one direction
Rotation in opposite direction
No rotation
Sequential trials
Nu
mb
er o
f p
ho
ton
sd
etec
ted
(
103)
0
20
25
30
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Fig. 9-15a
EXPERIMENT
Sample
Magnetic bead
Internalrod
Catalyticknob
Nickelplate
Electromagnet
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Fig. 9-15b
Rotation in one direction
Rotation in opposite direction
No rotation
Sequential trials
Nu
mb
er
of
ph
oto
ns
de
tec
ted
(x
10
3 )
30
25
20
0
RESULTS
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• The energy stored in a H+ gradient across a membrane couples the redox reactions of the electron transport chain to ATP synthesis
• The H+ gradient is referred to as a proton-motive force, emphasizing its capacity to do work
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Fig. 9-16
Protein complexof electroncarriers
H+
H+H+
Cyt c
Q
V
FADH2 FAD
NAD+NADH
(carrying electronsfrom food)
Electron transport chain
2 H+ + 1/2O2H2O
ADP + P i
Chemiosmosis
Oxidative phosphorylation
H+
H+
ATP synthase
ATP
21
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An Accounting of ATP Production by Cellular Respiration
• During cellular respiration, most energy flows in this sequence:
glucose NADH electron transport chain proton-motive force ATP
• About 40% of the energy in a glucose molecule is transferred to ATP during cellular respiration, making about 38 ATP
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Fig. 9-17
Maximum per glucose: About36 or 38 ATP
+ 2 ATP+ 2 ATP + about 32 or 34 ATP
Oxidativephosphorylation:electron transport
andchemiosmosis
Citricacidcycle
2AcetylCoA
Glycolysis
Glucose2
Pyruvate
2 NADH 2 NADH 6 NADH 2 FADH2
2 FADH2
2 NADHCYTOSOL Electron shuttles
span membrane
or
MITOCHONDRION
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Concept 9.5: Fermentation and anaerobic respiration enable cells to produce ATP withoutthe use of oxygen
• Most cellular respiration requires O2 to produce ATP
• Glycolysis can produce ATP with or without O2 (in aerobic or anaerobic conditions)
• In the absence of O2, glycolysis couples with fermentation or anaerobic respiration to produce ATP
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• Anaerobic respiration uses an electron transport chain with an electron acceptor other than O2, for example sulfate
• Fermentation uses phosphorylation instead of an electron transport chain to generate ATP
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Types of Fermentation
• Fermentation consists of glycolysis plus reactions that regenerate NAD+, which can be reused by glycolysis
• Two common types are alcohol fermentation and lactic acid fermentation
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• In alcohol fermentation, pyruvate is converted to ethanol in two steps, with the first releasing CO2
• Alcohol fermentation by yeast is used in brewing, winemaking, and baking
Animation: Fermentation OverviewAnimation: Fermentation Overview
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Fig. 9-18
2 ADP + 2 Pi 2 ATP
Glucose Glycolysis
2 NAD+ 2 NADH
2 Pyruvate
+ 2 H+
2 Acetaldehyde2 Ethanol
(a) Alcohol fermentation
2 ADP + 2 Pi2 ATP
Glucose Glycolysis
2 NAD+ 2 NADH+ 2 H+
2 Pyruvate
2 Lactate
(b) Lactic acid fermentation
2 CO2
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Fig. 9-18a
2 ADP + 2 P i 2 ATP
Glucose Glycolysis
2 Pyruvate
2 NADH2 NAD+
+ 2 H+CO2
2 Acetaldehyde2 Ethanol
(a) Alcohol fermentation
2
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• In lactic acid fermentation, pyruvate is reduced to NADH, forming lactate as an end product, with no release of CO2
• Lactic acid fermentation by some fungi and bacteria is used to make cheese and yogurt
• Human muscle cells use lactic acid fermentation to generate ATP when O2 is scarce
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Fig. 9-18b
Glucose
2 ADP + 2 P i 2 ATP
Glycolysis
2 NAD+ 2 NADH+ 2 H+
2 Pyruvate
2 Lactate
(b) Lactic acid fermentation
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Fermentation and Aerobic Respiration Compared
• Both processes use glycolysis to oxidize glucose and other organic fuels to pyruvate
• The processes have different final electron acceptors: an organic molecule (such as pyruvate or acetaldehyde) in fermentation and O2 in cellular respiration
• Cellular respiration produces 38 ATP per glucose molecule; fermentation produces 2 ATP per glucose molecule
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• Obligate anaerobes carry out fermentation or anaerobic respiration and cannot survive in the presence of O2
• Yeast and many bacteria are facultative anaerobes, meaning that they can survive using either fermentation or cellular respiration
• In a facultative anaerobe, pyruvate is a fork in the metabolic road that leads to two alternative catabolic routes
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Fig. 9-19Glucose
Glycolysis
Pyruvate
CYTOSOL
No O2 present:Fermentation
O2 present:
Aerobic cellular respiration
MITOCHONDRION
Acetyl CoAEthanolor
lactateCitricacidcycle
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The Evolutionary Significance of Glycolysis
• Glycolysis occurs in nearly all organisms
• Glycolysis probably evolved in ancient prokaryotes before there was oxygen in the atmosphere
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Concept 9.6: Glycolysis and the citric acid cycle connect to many other metabolic pathways
• Gycolysis and the citric acid cycle are major intersections to various catabolic and anabolic pathways
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The Versatility of Catabolism
• Catabolic pathways funnel electrons from many kinds of organic molecules into cellular respiration
• Glycolysis accepts a wide range of carbohydrates
• Proteins must be digested to amino acids; amino groups can feed glycolysis or the citric acid cycle
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• Fats are digested to glycerol (used in glycolysis) and fatty acids (used in generating acetyl CoA)
• Fatty acids are broken down by beta oxidation and yield acetyl CoA
• An oxidized gram of fat produces more than twice as much ATP as an oxidized gram of carbohydrate
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Fig. 9-20Proteins
Carbohydrates
Aminoacids
Sugars
Fats
Glycerol Fattyacids
Glycolysis
Glucose
Glyceraldehyde-3-
Pyruvate
P
NH3
Acetyl CoA
Citricacidcycle
Oxidativephosphorylation
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Biosynthesis (Anabolic Pathways)
• The body uses small molecules to build other substances
• These small molecules may come directly from food, from glycolysis, or from the citric acid cycle
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Regulation of Cellular Respiration via Feedback Mechanisms
• Feedback inhibition is the most common mechanism for control
• If ATP concentration begins to drop, respiration speeds up; when there is plenty of ATP, respiration slows down
• Control of catabolism is based mainly on regulating the activity of enzymes at strategic points in the catabolic pathway
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Fig. 9-21Glucose
GlycolysisFructose-6-phosphate
Phosphofructokinase
Fructose-1,6-bisphosphateInhibits
AMP
Stimulates
Inhibits
Pyruvate
CitrateAcetyl CoA
Citricacidcycle
Oxidativephosphorylation
ATP
+
––
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Fig. 9-UN5
Inputs
Glycolysis
Outputs
+
2
2
ATP
NADH
2Glucose Pyruvate
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Fig. 9-UN6
Inputs Outputs
Acetyl CoA2
2
2
2
6
ATP
NADH
FADH2
Oxaloacetate
Citric acidcycle
S—CoA
CH3
C O
O C COO
CH2
COO
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Fig. 9-UN7
INTER-MEMBRANESPACE
H+
ATPsynthase
ATPADP + P i
H+MITO-CHONDRIALMATRIX
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Fig. 9-UN8
pH
dif
fere
nce
acro
ss m
emb
ran
e
Time
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Fig. 9-UN9
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You should now be able to:
1. Explain in general terms how redox reactions are involved in energy exchanges
2. Name the three stages of cellular respiration; for each, state the region of the eukaryotic cell where it occurs and the products that result
3. In general terms, explain the role of the electron transport chain in cellular respiration
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4. Explain where and how the respiratory electron transport chain creates a proton gradient
5. Distinguish between fermentation and anaerobic respiration
6. Distinguish between obligate and facultative anaerobes
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