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Wavelength (nm) 400 450 500 550 600 650 700 L ig h t A b s o rb tio ...

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Copyr<strong>ig</strong>ht © The McGraw-Hill Companies, Inc. Permission required for reproduc<strong>tio</strong>n or display.<br />

Chloroplast<br />

Vascular bundle Stoma<br />

Vacuole<br />

Cell wall<br />

Inner membrane<br />

Outer membrane<br />

Courtesy Dr. Kenneth Miller, Brown University<br />

Cuticle<br />

Epidermis<br />

Mesophyll<br />

1.58 µm<br />

Copyr<strong>ig</strong>ht © The McGraw-Hill Companies, Inc. Permission required for reproduc<strong>tio</strong>n or display.<br />

0.001 <strong>nm</strong> 1 <strong>nm</strong> 10 <strong>nm</strong> 1000 <strong>nm</strong><br />

<strong>400</strong> <strong>nm</strong><br />

Gamma rays<br />

X-rays<br />

Increasing wavelength<br />

Visible l<strong>ig</strong>ht<br />

Increasing energy<br />

Infrared<br />

0.01 cm 1 cm 1 m<br />

Radio waves<br />

430 <strong>nm</strong> <strong>500</strong> <strong>nm</strong> 560 <strong>nm</strong> <strong>600</strong> <strong>nm</strong> <strong>650</strong> <strong>nm</strong> 740 <strong>nm</strong><br />

Porphyrin<br />

head<br />

UV<br />

l<strong>ig</strong>ht<br />

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H 2 C CH<br />

H 3 C<br />

H<br />

H 3 C<br />

H<br />

N N<br />

Mg<br />

N N<br />

H<br />

CO2CH3 O C<br />

O<br />

CH<br />

CCH3 CHCH3 CH2 CH2 CH2 CHCH3 CH2 CH2 CH2 CHCH3 CH3 O<br />

CH2 CH2 CH2 CH2 CH2 CH2 Hydroca<strong>rb</strong>on<br />

tail<br />

H<br />

H<br />

R<br />

Chlorophyll a: R = CH3 Chlorophyll b: R = CHO<br />

CH 2 CH 3<br />

H<br />

CH 3<br />

100 m<br />

1<br />

3<br />

5<br />

L<strong>ig</strong>ht<br />

Abso<strong>rb</strong><strong>tio</strong>n<br />

h<strong>ig</strong>h<br />

low<br />

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Photosystem<br />

Thylakoid<br />

Stroma<br />

Sunl<strong>ig</strong>ht<br />

ADP + P i<br />

CO 2<br />

L<strong>ig</strong>ht-Dependent<br />

Reac<strong>tio</strong>ns<br />

ATP<br />

H 2O<br />

Calvin<br />

Cycle<br />

NADP +<br />

O 2<br />

NADPH<br />

Organic<br />

molecules<br />

Copyr<strong>ig</strong>ht © The McGraw-Hill Companies, Inc. Permission required for reproduc<strong>tio</strong>n or display.<br />

carotenoids<br />

chlorophyll a<br />

chlorophyll b<br />

<strong>400</strong> <strong>450</strong> <strong>500</strong> <strong>550</strong> <strong>600</strong> <strong>650</strong> <strong>700</strong><br />

<strong>Wavelength</strong> (<strong>nm</strong>)<br />

Copyr<strong>ig</strong>ht © The McGraw-Hill Companies, Inc. Permission required for reproduc<strong>tio</strong>n or display.<br />

Oak leaf<br />

in summer<br />

Oak leaf<br />

in autumn<br />

© Eric Soder<br />

2<br />

4<br />

6


Energy of electrons<br />

Photon<br />

Chlorophyll<br />

molecule<br />

Excited reac<strong>tio</strong>n center<br />

Photon<br />

2 e –<br />

Photosystem II<br />

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Photosystem<br />

e –<br />

Electron<br />

donor<br />

e –<br />

Electron<br />

acceptor<br />

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2. The electrons pass through the b 6-f<br />

complex, which uses the energy<br />

released to pump protons across<br />

the thylakoid membrane. The proton<br />

gradient is used to produce ATP by<br />

chemiosmosis.<br />

e –<br />

2 Plastoquinone<br />

2<br />

e –<br />

b 6-f<br />

complex<br />

H 2O<br />

H +<br />

2H + + 1 / 2O2<br />

1. A pair of chlorophylls in the reac<strong>tio</strong>n center<br />

abso<strong>rb</strong> two photons of l<strong>ig</strong>ht. This excites two<br />

electrons that are transferred to plastoquinone<br />

(PQ). Loss of electrons from the reac<strong>tio</strong>n center<br />

produces an oxida<strong>tio</strong>n potential capable of<br />

oxidizing water.<br />

ADP + P i<br />

L<strong>ig</strong>ht-Dependent<br />

Reac<strong>tio</strong>ns<br />

Reac<strong>tio</strong>n<br />

center<br />

NADP +<br />

A T P<br />

Calvin<br />

Cycle<br />

PQ<br />

Proton gradient formed<br />

for ATP synthesis<br />

Plastocyanin<br />

PC<br />

Reac<strong>tio</strong>n center<br />

chlorophyll<br />

Thylakoid Thylakoid membrane membrane<br />

Excited reac<strong>tio</strong>n center<br />

2 e –<br />

Photosystem I<br />

2<br />

e –<br />

Reac<strong>tio</strong>n<br />

center<br />

Ferredoxin<br />

Fd<br />

NADP + + H +<br />

Photon<br />

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NADPH<br />

6 molecules of<br />

6 ADP<br />

6 ATP<br />

Ribulose 1,5-bisphosphate (5C) (RuBP)<br />

4 P i<br />

10 molecules of<br />

Glyceraldehyde 3-phosphate (3C)<br />

6 molecules of<br />

Ca<strong>rb</strong>on<br />

dioxide (CO 2 )<br />

Rubisco<br />

Calvin Cycle<br />

2 molecules of<br />

Glyceraldehyde 3-phosphate (3C) (G3P)<br />

Glucose and<br />

other sugars<br />

NADP<br />

reductase<br />

NADPH<br />

7<br />

3. A pair of chlorophylls in the reac<strong>tio</strong>n<br />

center abso<strong>rb</strong> two photons. This<br />

excites two electrons that are passed to<br />

NADP + , reducing it to NADPH. Electron<br />

transport from photosystem II replaces<br />

these electrons.<br />

12 molecules of<br />

3-phosphoglycerate (3C) (PGA)<br />

Stroma of chloroplast<br />

12 Pi 12 ATP<br />

12 ADP<br />

12 molecules of<br />

1,3-bisphosphoglycerate (3C)<br />

12 NADP +<br />

12 molecules of<br />

Glyceraldehyde 3-phosphate (3C) (G3P)<br />

12 NADPH<br />

9<br />

11<br />

L<strong>ig</strong>ht-Dependent<br />

Reac<strong>tio</strong>ns<br />

NADP<br />

ADP + P NADPH<br />

i ATP<br />

Stroma<br />

Calvin<br />

Cycle<br />

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e –<br />

+<br />

L<strong>ig</strong>ht<br />

e –<br />

Chlorophyll<br />

reduced<br />

Donor<br />

oxidized<br />

H 2O<br />

Water-splitting<br />

enzyme<br />

ADP + P i<br />

Thylakoid<br />

space<br />

e –<br />

–<br />

e –<br />

Electron<br />

donor<br />

Excited<br />

chlorophyll<br />

molecule<br />

e –<br />

+<br />

Electron<br />

acceptor<br />

Chlorophyll<br />

oxidized<br />

Acceptor<br />

reduced<br />

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Photon<br />

Thylakoid<br />

membrane<br />

2e –<br />

1 /2O2 2H+<br />

Antenna<br />

complex<br />

PQ<br />

Plastoquinone<br />

Photosystem II b6-f complex Photosystem I<br />

1. Photosystem II<br />

abso<strong>rb</strong>s photons,<br />

exciting electrons<br />

that are passed to<br />

plastoquinone (PQ).<br />

Electrons lost from<br />

photosystem II are<br />

replaced by the<br />

oxida<strong>tio</strong>n of water,<br />

producing O 2<br />

2e –<br />

H +<br />

Photon<br />

PC<br />

2. The b 6-f complex<br />

receives electrons<br />

from PQ and passes<br />

them to plastocyanin<br />

(PC). This provides<br />

energy for the b 6-f<br />

complex to pump<br />

protons into the<br />

thylakoid.<br />

2e–<br />

e –<br />

e –<br />

Plastocyanin Ferredoxin<br />

–<br />

e –<br />

+ NADP +<br />

H +<br />

Fd<br />

NADPH<br />

2e –<br />

NADP<br />

reductase<br />

3. Photosystem I abso<strong>rb</strong>s<br />

photons, exciting<br />

electrons that are<br />

passed through a<br />

carrier to reduce<br />

NADP + to NADPH.<br />

These electrons are<br />

replaced by electron<br />

transport from<br />

photosystem II.<br />

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Photo-<br />

system<br />

II<br />

Sunl<strong>ig</strong>ht<br />

O 2<br />

Heat<br />

ATP NADPH NAD NADH<br />

+<br />

NADPi Calvin<br />

Cycle<br />

Glucose<br />

Photo-<br />

system<br />

I<br />

ATP<br />

H 2 O<br />

CO 2<br />

Pyruvate<br />

Electron<br />

Transport<br />

System<br />

Krebs<br />

Cycle<br />

ADP<br />

Proton<br />

gradient<br />

H +<br />

H +<br />

H +<br />

H+<br />

ATP<br />

synthase<br />

ATP<br />

4. ATP synthase uses<br />

the proton gradient<br />

to synthesize ATP<br />

from ADP and P i<br />

enzyme acts as a<br />

channel for protons<br />

to diffuse back into<br />

the stroma using this<br />

energy to drive the<br />

synthesis of ATP.<br />

ATP<br />

ADP + P i<br />

ATP<br />

ADP + P i<br />

8<br />

10<br />

12


n<strong>ig</strong>ht<br />

day<br />

Mesophyll<br />

cell<br />

RuBP<br />

CO 2<br />

a. C 4 pathway<br />

Mesophyll<br />

cell<br />

Bundle-<br />

sheath<br />

cell<br />

Calvin<br />

Cycle<br />

G3P<br />

CO 2<br />

C 4<br />

CO 2<br />

Calvin<br />

Cycle<br />

G3<br />

b. C 4 pathway<br />

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3PG<br />

(C 3)<br />

Mesophyll cell Bundle-sheath cell<br />

Stoma<br />

Mesophyll cell<br />

Vein<br />

Stoma Vein<br />

a: © John Shaw/Photo Researchers, Inc. b: © Joseph Nettis/Na<strong>tio</strong>nal Audubon Society Collec<strong>tio</strong>n/Photo Researchers, Inc.<br />

CO 2<br />

C 4<br />

CO 2<br />

Calvin<br />

Cycle<br />

G3P<br />

Copyr<strong>ig</strong>ht © The McGraw-Hill Companies, Inc. Permission required for reproduc<strong>tio</strong>n or display.<br />

© ClydeH. Smith/Peter Arnold Inc.<br />

Bundle-<br />

sheath cell<br />

13<br />

15<br />

17<br />

Leaf<br />

epidermis<br />

H 2O<br />

Copyr<strong>ig</strong>ht © The McGraw-Hill Companies, Inc. Permission required for reproduc<strong>tio</strong>n or display.<br />

Heat<br />

Stomata<br />

H 2O<br />

Under hot, arid condi<strong>tio</strong>ns, leaves lose water by<br />

evapora<strong>tio</strong>n through openings in the leaves<br />

called stomata.<br />

CO 2<br />

O 2<br />

O 2<br />

CO 2<br />

The stomata close to conserve water but as a<br />

result, O 2 builds up inside the leaves, and CO 2<br />

cannot enter the leaves.<br />

Copyr<strong>ig</strong>ht © The McGraw-Hill Companies, Inc. Permission required for reproduc<strong>tio</strong>n or display.<br />

CO 2<br />

Mesophyll<br />

cell<br />

Phosphoenolpyruvate<br />

(PEP)<br />

AMP +<br />

PP i<br />

ATP<br />

+ P i<br />

Oxaloacetate<br />

Pyruvate Malate<br />

Pyruvate<br />

Bundle-sheath<br />

cell<br />

CO 2<br />

Calvin<br />

Cycle<br />

Glucose<br />

Malate<br />

14<br />

16

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