Photosynthesis CAMPBELL BIOLOGY IN FOCUS SECOND EDITION URRY CAIN WASSERMAN MINORSKY REECE

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CAMPBELL BIOLOGY IN FOCUS URRY CAIN WASSERMAN MINORSKY REECE 8 Photosynthesis Lecture Presentations by Kathleen Fitzpatrick and Nicole Tunbridge, Simon Fraser University SECOND EDITION

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

Autotrophs sustain themselves without eating anything derived from other organisms Autotrophs are the producers of the biosphere, producing organic molecules from CO 2 and other inorganic molecules Almost all plants are photoautotrophs, using the energy of sunlight to make organic molecules

Figure 8.1

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 O 2

Photosynthesis occurs in plants, algae, certain other protists, and some prokaryotes These organisms feed not only themselves but also most of the living world

Figure 8.2 10 mm 40 mm 1 mm (d) Cyanobacteria (a) Plants (b) Multicellular alga (e) Purple sulfur bacteria (c) Unicellular eukaryotes

Figure 8.2-1 (a) Plants

Figure 8.2-2 (b) Multicellular alga

Figure 8.2-3 10 mm (c) Unicellular eukaryotes

Figure 8.2-4 (d) Cyanobacteria 40 mm

Figure 8.2-5 1 mm (e) Purple sulfur bacteria

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

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

CO 2 enters and O 2 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

Figure 8.3 Leaf cross section Chloroplasts Vein Mesophyll Stomata CO 2 O 2 Chloroplast Mesophyll cell Thylakoid Thylakoid Stroma Granum space Outer membrane Intermembrane space Inner membrane 20 mm Chloroplast 1 mm

Figure 8.3-1 Leaf cross section Chloroplasts Vein Mesophyll Stomata CO 2 O 2

Figure 8.3-2 Chloroplast Mesophyll cell Stroma Thylakoid Granum Thylakoid space Outer membrane Intermembrane space Inner membrane 20 mm Chloroplast 1 mm

Figure 8.3-3 Mesophyll cell 20 mm

Figure 8.3-4 Stroma Granum Chloroplast 1 mm

Figure 8.3-5

Tracking Atoms Through Photosynthesis: Scientific Inquiry Photosynthesis is a complex series of reactions that can be summarized as the following equation 6 CO 2 12H 2 O Light energy C 6 H 12 O 6 6 O 2 6 H 2 O

The Splitting of Water Chloroplasts split H 2 O into hydrogen and oxygen, incorporating the electrons of hydrogen into sugar molecules and releasing oxygen as a by-product

Figure 8.4 Reactants: 6 CO 2 12 H 2 O Products: C 6 H 12 O 6 6 H 2 O 6 O 2

Photosynthesis as a Redox Process Photosynthesis reverses the direction of electron flow compared to respiration Photosynthesis is a redox process in which H 2 O is oxidized and CO 2 is reduced Photosynthesis is an endergonic process; the energy boost is provided by light

Figure 8.UN01 becomes reduced becomes oxidized

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 H 2 O Release O 2 Reduce the electron acceptor, NADP +, to NADPH Generate ATP from ADP by adding a phosphate group, photophosphorylation

The Calvin cycle (in the stroma) forms sugar from CO 2, using ATP and NADPH The Calvin cycle begins with carbon fixation, incorporating CO 2 into organic molecules

Animation: Photosynthesis

Figure 8.5-s1 Light H 2 O NADP LIGHT REACTIONS ADP P i Thylakoid Stroma Chloroplast

Figure 8.5-s2 Light H 2 O NADP LIGHT REACTIONS ADP P i Thylakoid ATP N AD PH Stroma Chloroplast O 2

Figure 8.5-s3 Light H 2 O CO 2 NADP LIGHT REACTIONS ADP P i CA L VIN CYCLE Thylakoid ATP N AD PH Stroma Chloroplast O 2 [CH 2 O] (sugar)

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

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

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

Figure 8.6 10-5 nm 10-3 nm 1 nm 10 3 nm 10 6 nm 1 m (10 9 nm) 10 3 m Gamma rays X-rays UV Infrared Microwaves Radio waves Visible light 380 450 500 550 600 650 700 750 nm Shorter wavelength Higher energy Longer wavelength Lower energy

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

Animation: Light and Pigments

Figure 8.7 Light Reflected light Chloroplast Absorbed light Granum Transmitted light

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

Figure 8.8 Technique White light Refracting prism Chlorophyll solution Photoelectric tube Galvanometer Slit moves to pass light of selected wavelength. Green light The high transmittance (low absorption) reading indicates that chlorophyll absorbs very little green light. Blue light The low transmittance (high absorption) reading indicates that chlorophyll absorbs most blue light.

An absorption spectrum is a graph that plots 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

Figure 8.9-1 Absorption of light by chloroplast pigments Chlorophyll a Chlorophyll b Carotenoids 400 500 600 700 Wavelength of light (nm) (a) Absorption spectra

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

Figure 8.9-2 Rate of photosynthesis (measured by O 2 release) 400 (b) Action spectrum 500 600 700

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 O 2 He used the growth of aerobic bacteria clustered along the alga as a measure of O 2 production

Figure 8.9-3 Aerobic bacteria Filament of alga 400 500 600 700 (c) Engelmann s experiment

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

Video: Chlorophyll Model

Figure 8.10 CH 3 CH 3 in chlorophyll a CHO in chlorophyll b Porphyrin ring: light-absorbing head of molecule; note magnesium atom at center Hydrocarbon tail: interacts with hydrophobic regions of proteins inside thylakoid membranes of chloroplasts; H atoms not shown

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

Figure 8.11 Energy of electron e - Excited state Heat Photon Chlorophyll molecule Photon (fluorescence) Ground state (a) Excitation of isolated chlorophyll molecule (b) Fluorescence

Figure 8.11-1 (b) Fluorescence

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

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

Figure 8.12 Thylakoid membrane Thylakoid membrane Photon Photosystem Light-harvesting complexes Reactioncenter complex STROMA Primary electron acceptor e - Chlorophyll (green) STROMA Transfer of energy (a) How a photosystem harvests light Special pair of Pigment chlorophyll a molecules molecules THYLAKOID SPACE (INTERIOR OF THYLAKOID) Protein subunits (purple) (b) Structure of a photosystem THYLAKOID SPACE

Thylakoid membrane Figure 8.12-1 Photon Photosystem Light-harvesting complexes Reactioncenter complex STROMA Primary electron acceptor e - Transfer of energy Special pair of chlorophyll a molecules Pigment molecules THYLAKOID SPACE (INTERIOR OF THYLAKOID) (a) How a photosystem harvests light

Figure 8.12-2 Thylakoid membrane Chlorophyll (green) STROMA Protein subunits (purple) (b) Structure of a photosystem THYLAKOID SPACE

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

Photosystem I (PS I) is best at absorbing a wavelength of 700 nm The reaction-center chlorophyll a of PS I is called P700 P680 and P700 are nearly identical, but their association with different proteins results in different light-absorbing properties

Linear Electron Flow Linear electron flow involves the flow of electrons through the photosystems and other molecules embedded in the thylakoid membrane to produce ATP and NADPH using light energy

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. H 2 O is split by enzymes, and the electrons are transferred from the hydrogen atoms to P680 +, thus reducing it to P680; O 2 is released as a by-product

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

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

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

Figure 8.UN02 H 2 O CO 2 Light LIGHT REACTIONS NADP ADP ATP CALVIN CYCLE NADPH O 2 [CH 2 O] (sugar)

Figure 8.13-s1 Primary acceptor e - P680 Light Photosystem II (PS II) Pigment molecules

Figure 8.13-s2 2 H 1 /2 O 2 Light H 2 O e - e - Primary acceptor e - P680 Photosystem II (PS II) Pigment molecules

Figure 8.13-s3 2 H 1 /2 O 2 H 2 O e - e - Primary acceptor e - P680 Electron transport chain Pq Cytochrome complex Pc Light ATP Photosystem II (PS II) Pigment molecules

Figure 8.13-s4 2 H 1 /2 O 2 Light H 2 O e - e - Primary acceptor P680 Electron transport chain Pq Cytochrome complex Pc Primary acceptor e - e- ATP P700 Light Photosystem II (PS II) Pigment molecules Photosystem I (PS I)

Figure 8.13-s5 2 H 1 /2 O 2 Light H 2 O e - e - Primary acceptor Electron transport chain Pq Cytochrome complex Pc Primary acceptor e - e- P680 ATP P700 Fd e - e - Electron transport chain NADP reductase Light NADP H NADPH Photosystem II (PS II) Pigment molecules Photosystem I (PS I)

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

Figure 8.14 e - e - e - e - Mill makes ATP e - e - NADPH e - ATP Photosystem II Photosystem I

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 there are also similarities Both use the energy generated by an electron transport chain to pump protons (H + ) across a membrane against their concentration gradient Both rely on the diffusion of protons through ATP synthase to drive the synthesis of ATP

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

Figure 8.15 Mitochondrion Chloroplast MITOCHONDRION STRUCTURE Intermembrane space Inner membrane Matrix Electron transport chain H ATP synthase Diffusion Thylakoid space Thylakoid membrane CHLOROPLAST STRUCTURE Stroma Higher [H ] ADP P i H ATP Lower [H ]

Figure 8.15-1 MITOCHONDRION STRUCTURE Intermembrane space Inner membrane Matrix Electron transport chain H ATP synthase Diffusion CHLOROPLAST STRUCTURE Thylakoid space Thylakoid membrane Stroma Higher [H ] Lower [H ] ADP P i H ATP

The light reactions of photosynthesis generate ATP and increase the potential energy of electrons by moving them from H 2 O to NADPH ATP and NADPH are produced on the side of the thylakoid membrane facing the stroma, where the Calvin cycle takes place The Calvin cycle uses ATP and NADPH to power the synthesis of sugar from CO 2

Figure 8.UN02 H 2 O CO 2 Light LIGHT REACTIONS NADP ADP ATP CALVIN CYCLE NADPH O 2 [CH 2 O] (sugar)

Figure 8.16 Photosystem II Cytochrome complex Photosystem I NADP reductase Light 4 H Light Fd NADP H H 2 O THYLAKOID SPACE (high H concentration) e e - - ½ O 2 2 H Pq 4 H Pc NADPH To Calvin Cycle STROMA (low H concentration) Thylakoid membrane ATP synthase ADP P H ATP i

Figure 8.16-1 Photosystem II Cytochrome complex Light 4 H Light Photosystem I Fd Pq H 2 O THYLAKOID SPACE (high H concentration) e - e - O 2 ½ 2 H 4 H Pc STROMA (low H concentration) Thylakoid membrane ATP synthase ADP P H ATP i

Figure 8.16-2 Cytochrome complex Light Photosystem I Fd NADP reductase NADP H Pc NADPH 4 H THYLAKOID SPACE (high H concentration) To Calvin Cycle ATP synthase ADP P i H ATP STROMA (low H concentration)

Concept 8.3: The Calvin cycle uses the chemical energy of ATP and NADPH to reduce CO 2 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

Carbon enters the cycle as CO 2 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 CO 2 The Calvin cycle has three phases Carbon fixation Reduction Regeneration of the CO 2 acceptor

Figure 8.UN03 Light H 2 O LIGHT REACTIONS NADP ADP ATP NADPH CO 2 CALVIN CYCLE O 2 [CH 2 O] (sugar)

Phase 1, carbon fixation, involves the incorporation of the CO 2 molecules into ribulose bisphosphate (RuBP) using the enzyme rubisco The product is 3-phosphoglycerate

Figure 8.17-s1 Input: Rubisco 3 CO 2, entering one per cycle Phase 1: Carbon fixation 3 P P 3 P P 6 P RuBP 3-Phosphoglycerate Calvin Cycle

Phase 2, reduction, involves the reduction and phosphorylation of 3-phosphoglycerate to G3P Six ATP and six NADPH are required to produce six molecules of G3P, but only one exits the cycle for use by the cell

Figure 8.17-s2 Input: Rubisco 3 CO 2, entering one per cycle Phase 1: Carbon fixation 3 P P 3 P P 6 P RuBP 3-Phosphoglycerate 6 ATP 6 ADP Calvin Cycle 6 P P 1,3-Bisphosphoglycerate 6 NADPH 6 6 NADP P i 6 P G3P Phase 2: Reduction Output: 1 G3P P Glucose and other organic compounds

Phase 3, regeneration, involves the rearrangement of the five remaining molecules of G3P to regenerate the initial CO 2 receptor, RuBP Three additional ATP are required to power this step

Figure 8.17-s3 Input: Rubisco 3 CO 2, entering one per cycle Phase 1: Carbon fixation 3 P P 3 P P 6 P RuBP 3-Phosphoglycerate 6 ATP 6 ADP 3 ATP 3 ADP Phase 3: Regeneration of RuBP 5 P Calvin Cycle 6 P 1,3-Bisphosphoglycerate 6 NADPH 6 6 NADP G3P 6 P G3P Phase 2: Reduction P P i Output: 1 G3P P Glucose and other organic compounds

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 H 2 O but also limits photosynthesis The closing of stomata reduces access to CO 2 and causes O 2 to build up These conditions favor an apparently wasteful process called photorespiration

In most plants (C 3 plants), initial fixation of CO 2, via rubisco, forms a three-carbon compound (3- phosphoglycerate) In photorespiration, rubisco adds O 2 instead of CO 2 in the Calvin cycle, producing a two-carbon compound Photorespiration decreases photosynthetic output by consuming ATP, O 2, and organic fuel and releasing CO 2 without producing any ATP or sugar

Photorespiration may be an evolutionary relic because rubisco first evolved at a time when the atmosphere had far less O 2 and more CO 2 Photorespiration limits damaging products of light reactions that build up in the absence of the Calvin cycle

C 4 Plants C 4 plants minimize the cost of photorespiration by incorporating CO 2 into a four-carbon compound An enzyme in the mesophyll cells has a high affinity for CO 2 and can fix carbon even when CO 2 concentrations are low These four-carbon compounds are exported to bundle-sheath cells, where they release CO 2 that is then used in the Calvin cycle

Figure 8.18a Sugarcane CO 2 C 4 Mesophyll cell Organic acid Bundlesheath cell CO 2 Calvin Cycle Sugar (a) Spatial separation of steps

Figure 8.18-1 Sugarcane

CAM Plants Some plants, including pineapples and many cacti and succulents, use crassulacean acid metabolism (CAM) to fix carbon CAM plants open their stomata at night, incorporating CO 2 into organic acids Stomata close during the day, and CO 2 is released from organic acids and used in the Calvin cycle

Figure 8.18b Pineapple Organic acid CO 2 Night CAM CO 2 Calvin Cycle Day Sugar (b) Temporal separation of steps

Figure 8.18-2 Pineapple

The C 4 and CAM pathways are similar in that they both incorporate carbon dioxide into organic intermediates before entering the Calvin cycle In C 4 plants, carbon fixation and the Calvin cycle occur in different cells In CAM plants, these processes occur in the same cells, but at different times of the day

Figure 8.18 Sugarcane Pineapple C 4 Mesophyll cell Organic acid CO 2 Organic acid CO 2 Night CAM Bundlesheath cell CO 2 Calvin Cycle CO 2 Calvin Cycle Day Sugar Sugar (a) Spatial separation of steps (b) Temporal separation of steps

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 O 2 in our atmosphere

Figure 8.19 Mesophyll cell Chloroplast O 2 CO 2 H 2 O Sucrose (export) Light H 2 O CO 2 LIGHT REACTIONS: Photosystem II Electron transport chain Photosystem I Electron transport chain NADP ADP P i ATP NADPH 3-Phosphoglycerate RuBP CALVIN CYCLE G3P Starch (storage) O 2 Sucrose (export) LIGHT REACTIONS Are carried out by molecules in the thylakoid membranes Convert light energy to the chemical energy of ATP and NADPH Split H 2 O and release O 2 CALVIN CYCLE REACTIONS Take place in the stroma Use ATP and NADPH to convert CO 2 to the sugar G3P Return ADP, inorganic phosphate, and NADP to the light reactions H 2 O

Figure 8.19-1 Light H 2 O CO 2 NADP LIGHT REACTIONS: Photosystem II Electron transport chain Photosystem I Electron transport chain ADP P i ATP RuBP 3-Phosphoglycerate CALVIN CYCLE G3P NADPH Starch (storage) O 2 Sucrose (export)

Figure 8.19-2 LIGHT REACTIONS CALVIN CYCLE REACTIONS Are carried out by molecules in the thylakoid membranes Convert light energy to the chemical energy of ATP and NADPH Split H 2 O and release O 2 Take place in the stroma Use ATP and NADPH to convert CO 2 to the sugar G3P Return ADP, inorganic phosphate, and NADP to the light reactions

Photosynthesis is one of many important processes conducted by a working plant cell

Figure 8.20 MAKE CONNECTIONS: The Working Cell Protein Nuclear pore Nucleus Ribosome mrna mrna DNA Rough endoplasmic Protein reticulum (ER) in vesicle Movement Across Cell Membranes (Chapter 5) Energy Transformations in the Cell: Photosynthesis and Cellular Respiration (Chapters 6-8) Vacuole Golgi apparatus Flow of Genetic Information in the Cell: DNA RNA Protein (Chapters 3 5) Plasma membrane Vesicle forming Cell wall Protein H 2 O Photosynthesis in chloroplast CO 2 H 2 O Organic molecules Cellular respiration in mitochondrion O 2 CO 2 O 2 ATP ATP ATP Transport pump ATP

Figure 8.20-1 Nucleus Nuclear pore mrna DNA Protein Ribosome mrna Protein in vesicle Rough endoplasmic reticulum (ER) Flow of Genetic Information in the Cell: DNA RNA Protein (Chapters 3-5)

Figure 8.20-2 Golgi apparatus Plasma membrane Vesicle forming Protein Cell wall Flow of Genetic Information in the Cell: DNA RNA Protein (Chapters 3-5)

Figure 8.20-3 Photosynthesis in chloroplast O 2 H 2 O CO 2 Organic molecules Cellular respiration in mitochondrion ATP ATP ATP ATP Transport pump Movement Across Cell Membranes (Chapter 5) H 2 O CO 2 O 2 Energy Transformations in the Cell: Photosynthesis and Cellular Respiration (Chapters 6-8)

Figure 8.UN04-1

Figure 8.UN04-2 Corn plant surrounded by invasive velvetleaf plants

Figure 8.UN05 H 2 O Primary acceptor Pq Primary acceptor Fd NADP reductase NADP H NADPH O 2 Cytochrome complex Pc Photosystem II ATP Photosystem I

Figure 8.UN06 3 CO 2 Carbon fixation 3 x 5C 6 x 3C Regeneration of CO 2 acceptor 5 x 3C Calvin Cycle Reduction 1 G3P (3C)

Figure 8.UN07 ph 7 ph 4 ph 4 ph 8 ATP

Figure 8.UN08