Urry • Cain • Wasserman • Minorsky • Jackson • Reece 8 · Autotrophs sustain themselves...

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CAMPBELL BIOLOGY IN FOCUS © 2014 Pearson Education, Inc. Urry Cain Wasserman Minorsky Jackson Reece Lecture Presentations by Kathleen Fitzpatrick and Nicole Tunbridge 8 Photosynthesis

Transcript of Urry • Cain • Wasserman • Minorsky • Jackson • Reece 8 · Autotrophs sustain themselves...

Page 1: Urry • Cain • Wasserman • Minorsky • Jackson • Reece 8 · Autotrophs sustain themselves without eating anything derived from other organisms Autotrophs are the producers

CAMPBELL BIOLOGY IN FOCUS

© 2014 Pearson Education, Inc.

Urry • Cain • Wasserman • Minorsky • Jackson • Reece

Lecture Presentations by Kathleen Fitzpatrick and Nicole Tunbridge

8Photosynthesis

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Overview: The Process That Feeds the Biosphere

Photosynthesis is the process that converts solar energy into chemical energy

Directly or indirectly, photosynthesis nourishes almost the entire living world

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Autotrophs sustain themselves without eating anything derived from other organisms

Autotrophs are the producers of the biosphere, producing organic molecules from CO2 and other inorganic molecules

Almost all plants are photoautotrophs, using the energy of sunlight to make organic molecules

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Figure 8.1

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Heterotrophs obtain their organic material from other organisms

Heterotrophs are the consumers of the biosphere

Almost all heterotrophs, including humans, depend on photoautotrophs for food and O2

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Photosynthesis occurs in plants, algae, certain other protists, and some prokaryotes

These organisms feed not only themselves but also most of the living world

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Figure 8.2

(a) Plants

(d) Cyanobacteria

(e) Purple sulfurbacteria

(b) Multicellularalga

(c) Unicellular eukaryotes10 µ

m

1 µ

m40

µm

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Figure 8.2a

(a) Plants

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Figure 8.2b

(b) Multicellular alga

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Figure 8.2c

(c) Unicellular eukaryotes10 µ

m

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Figure 8.2d

(d) Cyanobacteria

40 µ

m

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Figure 8.2e

(e) Purple sulfurbacteria

1 µ

m

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Concept 8.1: Photosynthesis converts light energy to the chemical energy of food

The structural organization of photosynthetic cells includes enzymes and other molecules grouped together in a membrane

This organization allows for the chemical reactions of photosynthesis to proceed efficiently

Chloroplasts are structurally similar to and likely evolved from photosynthetic bacteria

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Chloroplasts: The Sites of Photosynthesis in Plants

Leaves are the major locations of photosynthesis

Their green color is from chlorophyll, the green pigment within chloroplasts

Chloroplasts are found mainly in cells of the mesophyll, the interior tissue of the leaf

Each mesophyll cell contains 30–40 chloroplasts

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CO2 enters and O2 exits the leaf through microscopic pores called stomata

The chlorophyll is in the membranes of thylakoids (connected sacs in the chloroplast); thylakoids may be stacked in columns called grana

Chloroplasts also contain stroma, a dense interior fluid

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Figure 8.3Leaf cross section

20 µm

Mesophyll

Stomata

Chloroplasts Vein

CO2 O2

Mesophyll cell

Chloroplast

Stroma

Thylakoid

Thylakoidspace

Outermembrane

Intermembranespace

Inner membrane

Granum

1 µm

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Figure 8.3a

Leaf cross section

Mesophyll

Stomata

Chloroplasts Vein

CO2 O2

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Figure 8.3b

20 µm

Mesophyll cellChloroplast

Stroma

Thylakoid

Thylakoidspace

Outermembrane

Intermembranespace

Inner membrane

Granum

1 µm

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Figure 8.3c

20 µm

Mesophyll cell

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Figure 8.3d

StromaGranum

1 µm

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Tracking Atoms Through Photosynthesis: Scientific Inquiry

Photosynthesis is a complex series of reactions that can be summarized as the following equation

6 CO2 + 12 H2O + Light energy → C6H12O6 + 6 O2 + 6 H2O

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The Splitting of Water

Chloroplasts split H2O into hydrogen and oxygen, incorporating the electrons of hydrogen into sugar molecules and releasing oxygen as a by-product

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Figure 8.4

Products:

Reactants: 6 CO2

6 O2C6H12O6 6 H2O

12 H2O

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Photosynthesis as a Redox Process

Photosynthesis reverses the direction of electron flow compared to respiration

Photosynthesis is a redox process in which H2O is oxidized and CO2 is reduced

Photosynthesis is an endergonic process; the energy boost is provided by light

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Figure 8.UN01

becomes reduced

becomes oxidized

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The Two Stages of Photosynthesis: A Preview

Photosynthesis consists of the light reactions (the photo part) and Calvin cycle (the synthesis part)

The light reactions (in the thylakoids)

Split H2O

Release O2

Reduce the electron acceptor, NADP+, to NADPH

Generate ATP from ADP by adding a phosphate group, photophosphorylation

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The Calvin cycle (in the stroma) forms sugar from CO2, using ATP and NADPH

The Calvin cycle begins with carbon fixation, incorporating CO2 into organic molecules

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Animation: Photosynthesis

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Figure 8.5

Light

CO2H2O

P i

Chloroplast

LightReactions

CalvinCycle

[CH2O](sugar)

O2

ADP

ATP

NADP+

+

NADPH

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Figure 8.5-1

Light

H2O

Chloroplast

LightReactions

P i

ADP

NADP+

+

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Figure 8.5-2

Light

H2O

P i

Chloroplast

LightReactions

O2

ADP

ATP

NADP+

+

NADPH

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Figure 8.5-3

Light

CO2H2O

P i

Chloroplast

LightReactions

CalvinCycle

O2

ADP

ATP

NADP+

+

NADPH

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Figure 8.5-4

Light

CO2H2O

P i

Chloroplast

LightReactions

CalvinCycle

[CH2O](sugar)

O2

ADP

ATP

NADP+

+

NADPH

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Concept 8.2: The light reactions convert solar energy to the chemical energy of ATP and NADPH

Chloroplasts are solar-powered chemical factories

Their thylakoids transform light energy into the chemical energy of ATP and NADPH

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The Nature of Sunlight

Light is a form of electromagnetic energy, also called electromagnetic radiation

Like other electromagnetic energy, light travels in rhythmic waves

Wavelength is the distance between crests of waves

Wavelength determines the type of electromagnetic energy

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The electromagnetic spectrum is the entire range of electromagnetic energy, or radiation

Visible light consists of wavelengths (including those that drive photosynthesis) that produce colors we can see

Light also behaves as though it consists of discrete particles, called photons

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Figure 8.6

Gammarays

10−5 nm 10−3 nm 1 nm 103 nm 106 nm1 m

(109 nm) 103 m

Radiowaves

Micro-wavesX-rays InfraredUV

Visible light

Shorter wavelength Longer wavelength

Lower energyHigher energy

380 450 500 550 650600 700 750 nm

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Photosynthetic Pigments: The Light Receptors

Pigments are substances that absorb visible light

Different pigments absorb different wavelengths

Wavelengths that are not absorbed are reflected or transmitted

Leaves appear green because chlorophyll reflects and transmits green light

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Animation: Light and Pigments

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Figure 8.7

Reflectedlight

Light

Absorbedlight

Chloroplast

Granum

Transmittedlight

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A spectrophotometer measures a pigment’s ability to absorb various wavelengths

This machine sends light through pigments and measures the fraction of light transmitted at each wavelength

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Figure 8.8

Refractingprism

Whitelight

Greenlight

Bluelight

Chlorophyllsolution

Photoelectrictube

Galvanometer

Slit moves to passlight of selectedwavelength.

The low transmittance (highabsorption) reading indicatesthat chlorophyll absorbs mostblue light.

The high transmittance (lowabsorption) reading indicatesthat chlorophyll absorbs verylittle green light.

Technique

1

2

4

3

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An absorption spectrum is a graph plotting a pigment’s light absorption versus wavelength

The absorption spectrum of chlorophyll a suggests that violet-blue and red light work best for photosynthesis

Accessory pigments include chlorophyll b and a group of pigments called carotenoids

An action spectrum profiles the relative effectiveness of different wavelengths of radiation in driving a process

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Figure 8.9

Chloro-phyll a

Rat

e o

fp

ho

tosy

nth

esis

(mea

sure

d b

y O

2

rele

ase)

Results

Ab

so

rpti

on

of

lig

ht

by

chlo

rop

last

pig

men

ts

Chlorophyll b

Carotenoids

Filamentof alga

Aerobic bacteria

(a) Absorption spectra

(b) Action spectrum

(c) Engelmann’s experiment

400 700600500

400 700600500

400 700600500

Wavelength of light (nm)

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Figure 8.9a

Chloro-phyll a

Ab

sorp

tio

n o

f li

gh

tb

y ch

loro

pla

stp

igm

ents

Chlorophyll b

Carotenoids

(a) Absorption spectra

400 700600500

Wavelength of light (nm)

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Figure 8.9b

(b) Action spectrum

400 700600500

Rat

e o

fp

ho

tosy

nth

esi

s(m

eas

ure

d b

y O

2

rele

ase

)

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Figure 8.9c

Filamentof alga

Aerobic bacteria

(c) Engelmann’s experiment400 700600500

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The action spectrum of photosynthesis was first demonstrated in 1883 by Theodor W. Engelmann

In his experiment, he exposed different segments of a filamentous alga to different wavelengths

Areas receiving wavelengths favorable to photosynthesis produced excess O2

He used the growth of aerobic bacteria clustered along the alga as a measure of O2 production

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Chlorophyll a is the main photosynthetic pigment

Accessory pigments, such as chlorophyll b, broaden the spectrum used for photosynthesis

A slight structural difference between chlorophyll a and chlorophyll b causes them to absorb slightly different wavelengths

Accessory pigments called carotenoids absorb excessive light that would damage chlorophyll

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Video: Chlorophyll Model

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Figure 8.10

Hydrocarbon tail:interacts with hydrophobicregions of proteins insidethylakoid membranes ofchloroplasts; H atoms notshown

Porphyrin ring:light-absorbing“head” of molecule;note magnesiumatom at center

CH3 in chlorophyll aCHO in chlorophyll bCH3

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Excitation of Chlorophyll by Light

When a pigment absorbs light, it goes from a ground state to an excited state, which is unstable

When excited electrons fall back to the ground state, photons are given off, an afterglow called fluorescence

If illuminated, an isolated solution of chlorophyll will fluoresce, giving off light and heat

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Figure 8.11

Photon(fluorescence)

Groundstate

(b) Fluorescence

Excitedstate

Chlorophyllmolecule

Photon

Heat

e−

(a) Excitation of isolated chlorophyll molecule

En

erg

y o

f el

ectr

on

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Figure 8.11a

(b) Fluorescence

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A Photosystem: A Reaction-Center Complex Associated with Light-Harvesting Complexes

A photosystem consists of a reaction-center complex (a type of protein complex) surrounded by light-harvesting complexes

The light-harvesting complexes (pigment molecules bound to proteins) transfer the energy of photons to the reaction center

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Figure 8.12

(b) Structure of a photosystem(a) How a photosystem harvests light

Chlorophyll STROMA

THYLAKOIDSPACE

Proteinsubunits

STROMA

THYLAKOID SPACE(INTERIOR OF THYLAKOID)

PhotosystemPhoton

Light-harvestingcomplexes

Reaction-centercomplex

Primaryelectronacceptor

Special pair ofchlorophyll amolecules

Transferof energy

Pigmentmolecules

Th

ylak

oid

mem

bra

ne

Th

ylak

oid

mem

bra

nee−

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Figure 8.12a

(a) How a photosystem harvests light

STROMA

THYLAKOID SPACE(INTERIOR OF THYLAKOID)

PhotosystemPhoton

Light-harvestingcomplexes

Reaction-centercomplex

Primaryelectronacceptor

Special pair ofchlorophyll amolecules

Transferof energy

Pigmentmolecules

Th

ylak

oid

mem

bra

ne

e−

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Figure 8.12b

(b) Structure of a photosystem

Chlorophyll STROMA

THYLAKOID SPACE

Proteinsubunits

Th

ylak

oid

mem

bra

ne

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A primary electron acceptor in the reaction center accepts excited electrons and is reduced as a result

Solar-powered transfer of an electron from a chlorophyll a molecule to the primary electron acceptor is the first step of the light reactions

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There are two types of photosystems in the thylakoid membrane

Photosystem II (PS II) functions first (the numbers reflect order of discovery) and is best at absorbing a wavelength of 680 nm

The reaction-center chlorophyll a of PS II is called P680

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Photosystem I (PS I) is best at absorbing a wavelength of 700 nm

The reaction-center chlorophyll a of PS I is called P700

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Linear Electron Flow

Linear electron flow involves the flow of electrons through both photosystems to produce ATP and NADPH using light energy

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Linear electron flow can be broken down into a series of steps

1. A photon hits a pigment and its energy is passed among pigment molecules until it excites P680

2. An excited electron from P680 is transferred to the primary electron acceptor (we now call it P680+)

3. H2O is split by enzymes, and the electrons are transferred from the hydrogen atoms to P680+, thus reducing it to P680; O2 is released as a by-product

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Figure 8.UN02

CalvinCycle

NADPH

NADP+

ATP

ADP

Light

CO2

[CH2O] (sugar)

LightReactions

O2

H2O

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Figure 8.13-1

Primaryacceptor

Photosystem II(PS II)

Light

P680

Pigmentmolecules

1

2e−

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Figure 8.13-2

Primaryacceptor

2 H+

O2

+

Photosystem II(PS II)

H2O

Light

/2

1

P680

Pigmentmolecules

1

2

3

e−

e−

e−

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Figure 8.13-3

Primaryacceptor

2 H+

O2

+

ATP

Photosystem II(PS II)

H2O

Light

/2

1

P680

Pq

Electrontransportchain

Cytochromecomplex

Pc

Pigmentmolecules

1

2

3

4

5

e−

e−

e−

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Figure 8.13-4

Primaryacceptor

2 H+

O2

+

ATP

Photosystem II(PS II)

H2O

Light

/2

1

P680

Pq

Electrontransportchain

Cytochromecomplex

Pc

Pigmentmolecules

Primaryacceptor

Photosystem I(PS I)

P700

Light1

2

3

4

5

6

e−

e−

e−

e−

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Figure 8.13-5

Primaryacceptor

2 H+

O2

+

ATP

NADPH

Photosystem II(PS II)

H2Oe−

e−

e−

Light

/2

1

P680

Pq

Electrontransportchain

Cytochromecomplex

Pc

Pigmentmolecules

Primaryacceptor

Photosystem I(PS I)

e−

P700

e−

e−

Fd

Light

Electrontransportchain

H++NADP+

NADP+

reductase

1

2

3

4

5

6

7

8

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4. Each electron “falls” down an electron transport chain from the primary electron acceptor of PS II to PS I

5. Energy released by the fall drives the creation of a proton gradient across the thylakoid membrane; diffusion of H+ (protons) across the membrane drives ATP synthesis

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6. In PS I (like PS II), transferred light energy excites P700, causing it to lose an electron to an electron acceptor (we now call it P700+)

P700+ accepts an electron passed down from PS II via the electron transport chain

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7. Excited electrons “fall” down an electron transport chain from the primary electron acceptor of PS I to the protein ferredoxin (Fd)

8. The electrons are transferred to NADP+, reducing it to NADPH, and become available for the reactions of the Calvin cycle

This process also removes an H+ from the stroma

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The energy changes of electrons during linear flow can be represented in a mechanical analogy

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Figure 8.14

Photosystem II Photosystem I

NADPH

Millmakes

ATP

Ph

oto

n

Ph

oto

n

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A Comparison of Chemiosmosis in Chloroplasts and Mitochondria

Chloroplasts and mitochondria generate ATP by chemiosmosis but use different sources of energy

Mitochondria transfer chemical energy from food to ATP; chloroplasts transform light energy into the chemical energy of ATP

Spatial organization of chemiosmosis differs between chloroplasts and mitochondria but also shows similarities

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In mitochondria, protons are pumped to the intermembrane space and drive ATP synthesis as they diffuse back into the mitochondrial matrix

In chloroplasts, protons are pumped into the thylakoid space and drive ATP synthesis as they diffuse back into the stroma

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Figure 8.15

Electrontransport

chain

Higher [H+]P i

H+

CHLOROPLASTSTRUCTURE

Inter-membrane

space

MITOCHONDRIONSTRUCTURE

Thylakoidspace

Innermembrane

Matrix

Key

Lower [H+]

Thylakoidmembrane

Stroma

ATP

ATPsynthase

ADP +

H+ Diffusion

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Figure 8.15a

Electrontransport

chain

Higher [H+] H+

CHLOROPLASTSTRUCTURE

Inter-membrane

space

MITOCHONDRIONSTRUCTURE

Thylakoidspace

Innermembrane

MatrixKey

Lower [H+]

Thylakoidmembrane

Stroma

ATP

ATPsynthase

ADP +

H+ Diffusion

Pi

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ATP and NADPH are produced on the side facing the stroma, where the Calvin cycle takes place

In summary, light reactions generate ATP and increase the potential energy of electrons by moving them from H2O to NADPH

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Figure 8.UN02

CalvinCycle

NADPH

NADP+

ATP

ADP

Light

CO2

[CH2O] (sugar)

LightReactions

O2

H2O

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Figure 8.16

Photosystem II Photosystem I

ToCalvinCycle

H+

THYLAKOID SPACE(high H+ concentration)

Thylakoidmembrane

STROMA(low H+ concentration)

ATPsynthase

NADPH

e−

LightNADP+

ATPADP

+

NADP+

reductase

FdH++

Pq

Pc

Cytochromecomplex

4 H+

Light

+2 H+O2

H2O/21

4 H+

e−

1

2

3

Pi

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Figure 8.16a

Photosystem II Photosystem I

H+

THYLAKOID SPACE(high H+ concentration)

Thylakoidmembrane

STROMA(low H+ concentration)

ATPsynthase

e−

Light

ATPADP

+

Fd

Pq

Pc

Cytochromecomplex

4 H+

Light

+2 H+

O2

H2O/2

1

4 H+

e−

1

2

Pi

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Figure 8.16b

2

3Photosystem I

ToCalvinCycle

H+

ATPsynthase

NADPH

LightNADP+

ATPADP

+

NADP+

reductase

FdH++

Pc

Cytochromecomplex

4 H+

THYLAKOID SPACE(high H+ concentration)

STROMA(low H+ concentration)

Pi

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Concept 8.3: The Calvin cycle uses the chemical energy of ATP and NADPH to reduce CO2 to sugar

The Calvin cycle, like the citric acid cycle, regenerates its starting material after molecules enter and leave the cycle

Unlike the citric acid cycle, the Calvin cycle is anabolic

It builds sugar from smaller molecules by using ATP and the reducing power of electrons carried by NADPH

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Carbon enters the cycle as CO2 and leaves as a sugar named glyceraldehyde 3-phospate (G3P)

For net synthesis of one G3P, the cycle must take place three times, fixing three molecules of CO2

The Calvin cycle has three phases

Carbon fixation

Reduction

Regeneration of the CO2 acceptor

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Phase 1, carbon fixation, involves the incorporation of the CO2 molecules into ribulose bisphosphate (RuBP) using the enzyme rubisco

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Figure 8.UN03

CalvinCycle

NADPH

NADP+

ATP

ADP

Light

CO2

[CH2O] (sugar)

LightReactions

O2

H2O

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Figure 8.17-1Input 3

CalvinCycle

as 3 CO2

Rubisco Phase 1: Carbon fixation

RuBP 3-Phosphoglycerate6

3

3 P

P

P P

P

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Figure 8.17-2

6 P i

NADPH

Input 3

ATP

CalvinCycle

as 3 CO2

Rubisco Phase 1: Carbon fixation

Phase 2: Reduction

G3POutput

Glucose and other organiccompounds

G3P

RuBP 3-Phosphoglycerate

1,3-Bisphosphoglycerate

6 ADP

6

6

6

6

3

6 NADP+

6

3

1

P

P P

P

P

P P

P

P

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Figure 8.17-3

6 P i

NADPH

Input 3

ATP

CalvinCycle

as 3 CO2

Rubisco Phase 1: Carbon fixation

Phase 2: Reduction

Phase 3: Regenerationof RuBP

G3POutput

Glucose and other organiccompounds

G3P

RuBP 3-Phosphoglycerate

1,3-Bisphosphoglycerate

6 ADP

6

6

6

6 P

3

P P

P

6 NADP+

6 P

5 P

G3P

ATP

3 ADP

3

3 P P

1 P

P

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Phase 2, reduction, involves the reduction and phosphorylation of 3-phosphoglycerate to G3P

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Phase 3, regeneration, involves the rearrangement of G3P to regenerate the initial CO2 receptor, RuBP

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Evolution of Alternative Mechanisms of Carbon Fixation in Hot, Arid Climates

Adaptation to dehydration is a problem for land plants, sometimes requiring trade-offs with other metabolic processes, especially photosynthesis

On hot, dry days, plants close stomata, which conserves H2O but also limits photosynthesis

The closing of stomata reduces access to CO2 and causes O2 to build up

These conditions favor an apparently wasteful process called photorespiration

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In most plants (C3 plants), initial fixation of CO2, via rubisco, forms a three-carbon compound (3-phosphoglycerate)

In photorespiration, rubisco adds O2 instead of CO2 in the Calvin cycle, producing a two-carbon compound

Photorespiration decreases photosynthetic output by consuming ATP, O2, and organic fuel and releasing CO2 without producing any ATP or sugar

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Photorespiration may be an evolutionary relic because rubisco first evolved at a time when the atmosphere had far less O2 and more CO2

Photorespiration limits damaging products of light reactions that build up in the absence of the Calvin cycle

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C4 plants minimize the cost of photorespiration by incorporating CO2 into a four-carbon compound

An enzyme in the mesophyll cells has a high affinity for CO2 and can fix carbon even when CO2 concentrations are low

These four-carbon compounds are exported to bundle-sheath cells, where they release CO2 that is then used in the Calvin cycle

C4 Plants

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Figure 8.18

Bundle-sheathcell

Sugarcane

CO2

Pineapple

CO2

(a) Spatial separation of steps

C4

CO2CO2

CAM

Day

Night

Sugar

CalvinCycle

CalvinCycle

Sugar

Organicacid

Organicacid

Mesophyllcell

(b) Temporal separation of steps

1

2

1

2

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Figure 8.18a

Sugarcane

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Figure 8.18b

Pineapple

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Figure 8.18c

Bundle-sheathcell

CO2CO2

(a) Spatial separation of steps

C4

CO2CO2

CAM

Day

Night

Sugar

CalvinCycle

CalvinCycle

Sugar

Organicacid

Organicacid

Mesophyllcell

(b) Temporal separation of steps

1

2

1

2

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CAM Plants

Some plants, including succulents, use crassulacean acid metabolism (CAM) to fix carbon

CAM plants open their stomata at night, incorporating CO2 into organic acids

Stomata close during the day, and CO2 is released from organic acids and used in the Calvin cycle

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The Importance of Photosynthesis: A Review

The energy entering chloroplasts as sunlight gets stored as chemical energy in organic compounds

Sugar made in the chloroplasts supplies chemical energy and carbon skeletons to synthesize the organic molecules of cells

Plants store excess sugar as starch in the chloroplasts and in structures such as roots, tubers, seeds, and fruits

In addition to food production, photosynthesis produces the O2 in our atmosphere

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Figure 8.19

Photosystem IIElectron transport chain

CalvinCycle

NADPH

LightNADP+

ATP

CO2H2O

ADP+

3-Phosphpglycerate

G3P

RuBP

Sucrose (export)

Starch(storage)

Chloroplast

O2

LightReactions:

Photosystem IElectron transport chain

Pi

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Figure 8.UN04

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Figure 8.UN05

Photosystem II

Photosystem I

NADP+

ATP

Fd

H++Pq

Cytochromecomplex

O2

H2O

Pc

NADP+

reductaseNADPH

Primaryacceptor

Electron transport

chain

Primaryacceptor

Electron transport

chain

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Figure 8.UN06

CalvinCycle

Regeneration ofCO2 acceptor

Carbon fixation

Reduction

1 G3P (3C)

3 CO2

3 × 5C 6 × 3C

5 × 3C

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Figure 8.UN07

pH 7

pH 4 pH 8

pH 4