1. BIO 3A Spring 2011 Chapter 10 Photosynthesis

2. 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

3. 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

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

6. (a) Plants (b)Multicellular alga (c)Unicellular protists (d) Cyanobacteria (e)Purple sulfur bacteria 10  m 1  m 40  m Figure 10.2

7. 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

8. The Earth’s supply of fossil fuels was formed from the remains of organisms that died hundreds of millions of years ago In a sense, fossil fuels represent stores of solar energy from the distant past

10. 1: Photosynthesis converts light energy to the chemical energy of food Chloroplasts are structurally similar to and likely evolved from photosynthetic bacteria The structural organization of these cells allows for the chemical reactions of photosynthesis

11. 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

12. 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

13. Figure 10.4 Mesophyll Leaf cross section Chloroplasts Vein Stomata Chloroplast Mesophyll cell CO 2 O2O2 20  m Outer membrane Intermembrane space Inner membrane 1  m Thylakoid space Thylakoid Granum Stroma

14. 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

15. Reactants: Products: 6 CO 2 6 H 2 O 6 O 2 12 H 2 O C 6 H 12 O 6

16. 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

17. Energy  6 CO 2  6 H 2 O C 6 H 12 O 6  6 O 2 becomes reduced becomes oxidized

18. 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 NADP + to NADPH –Generate ATP from ADP by photophosphorylation

19. 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

20. Light Light Reactions Chloroplast NADP  ADP + P i H2OH2O Figure 10.6-1

21. Light Light Reactions Chloroplast ATP NADPH NADP  ADP + P i H2OH2O O2O2 Figure 10.6-2

22. Light Light Reactions Calvin Cycle Chloroplast ATP NADPH NADP  ADP + P i H2OH2O CO 2 O2O2 Figure 10.6-3

23. Light Light Reactions Calvin Cycle Chloroplast [CH 2 O] (sugar) ATP NADPH NADP  ADP + P i H2OH2O CO 2 O2O2 Figure 10.6-4

24. 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

25. 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

26. 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 © 2011 Pearson Education, Inc.

27. Gamma rays X-rays UV Infrared Micro- waves Radio waves Visible light Shorter wavelength Longer wavelength Lower energy Higher energy 380 450500 550600650 700 750 nm 10  5 nm 10  3 nm 1 nm 10 3 nm 10 6 nm (10 9 nm) 10 3 m 1 m

28. 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

29. Chloroplast Light Reflected light Absorbed light Transmitted light Granum

30. 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

31. White light Refracting prism Chlorophyll solution Photoelectric tube Galvanometer Slit moves to pass light of selected wavelength. Green light High transmittance (low absorption): Chlorophyll absorbs very little green light. Blue light Low transmittance (high absorption): Chlorophyll absorbs most blue light. TECHNIQUE

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

33. (b) Action spectrum (a) Absorption spectra Engelmann’s experiment (c) Chloro- phyll a Chlorophyll b Carotenoids Wavelength of light (nm) Absorption of light by chloroplast pigments Rate of photosynthesis (measured by O 2 release) Aerobic bacteria Filament of alga 400 500600700 400 500600700 400 500600700 RESULTS

34. 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

35. Chlorophyll a is the main photosynthetic pigment Accessory pigments, such as chlorophyll b, broaden the spectrum used for photosynthesis Accessory pigments called carotenoids absorb excessive light that would damage chlorophyll

36. Hydrocarbon tail (H atoms not shown) Porphyrin ring CH 3 CH 3 in chlorophyll a CHO in chlorophyll b

37. 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

38. Excited state Heat ee Photon (fluorescence) Ground state Photon Chlorophyll molecule Energy of electron (a) Excitation of isolated chlorophyll molecule (b) Fluorescence

39. 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

40. Figure 10.13 (b) Structure of photosystem II (a) How a photosystem harvests light Thylakoid membrane Photon Photosystem STROMA Light- harvesting complexes Reaction- center complex Primary electron acceptor Transfer of energy Special pair of chlorophyll a molecules Pigment molecules THYLAKOID SPACE (INTERIOR OF THYLAKOID) Chlorophyll STROMA Protein subunits THYLAKOID SPACE ee

41. 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

42. 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

43. Photosystem I (PS I) is best at absorbing a wavelength of 700 nm The reaction-center chlorophyll a of PS I is called P700

44. Linear Electron Flow During the light reactions, there are two possible routes for electron flow: cyclic and linear Linear electron flow, the primary pathway, involves both photosystems and produces ATP and NADPH using light energy

45. A photon hits a pigment and its energy is passed among pigment molecules until it excites P680 An excited electron from P680 is transferred to the primary electron acceptor (we now call it P680 + )

46. Figure 10.14-1 Primary acceptor P680 Light Pigment molecules Photosystem II (PS II ) 1 2 ee

47. P680 + is a very strong oxidizing agent 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 of this reaction

48. Figure 10.14-2 Primary acceptor H2OH2O O2O2 2 H  + 1/21/2 P680 Light Pigment molecules Photosystem II (PS II ) 1 23 ee ee ee

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

50. Figure 10.14-3 Cytochrome complex Primary acceptor H2OH2O O2O2 2 H  + 1/21/2 P680 Light Pigment molecules Photosystem II (PS II ) Pq Pc ATP 1 235 Electron transport chain ee ee ee 4

51. In PS I (like PS II), transferred light energy excites P700, which loses an electron to an electron acceptor P700 + (P700 that is missing an electron) accepts an electron passed down from PS II via the electron transport chain

52. Figure 10.14-4 Cytochrome complex Primary acceptor H2OH2O O2O2 2 H  + 1/21/2 P680 Light Pigment molecules Photosystem II (PS II ) Photosystem I (PS I ) Pq Pc ATP 1 235 6 Electron transport chain P700 Light ee ee 4 ee ee

53. Each electron “falls” down an electron transport chain from the primary electron acceptor of PS I to the protein ferredoxin (Fd) The electrons are then transferred to NADP + and reduce it to NADPH The electrons of NADPH are available for the reactions of the Calvin cycle This process also removes an H + from the stroma

54. Figure 10.14-5 Cytochrome complex Primary acceptor H2OH2O O2O2 2 H  + 1/21/2 P680 Light Pigment molecules Photosystem II (PS II ) Photosystem I (PS I ) Pq Pc ATP 1 235 6 7 8 Electron transport chain P700 Light + H  NADP  NADPH NADP  reductase Fd ee ee ee ee 4 ee ee

55. Photosystem II Photosystem I Mill makes ATP ATP NADPH ee ee ee ee ee ee ee Photon Figure 10.15

56. Cyclic Electron Flow Cyclic electron flow uses only photosystem I and produces ATP, but not NADPH No oxygen is released Cyclic electron flow generates surplus ATP, satisfying the higher demand in the Calvin cycle

57. Figure 10.16 Photosystem I Primary acceptor Cytochrome complex Fd Pc ATP Primary acceptor Pq Fd NADPH NADP  reductase NADP  + H  Photosystem II

58. Some organisms such as purple sulfur bacteria have PS I but not PS II Cyclic electron flow is thought to have evolved before linear electron flow Cyclic electron flow may protect cells from light-induced damage © 2011 Pearson Education, Inc.

59. 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

60. 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

61. Mitochondrion Chloroplast MITOCHONDRION STRUCTURE CHLOROPLAST STRUCTURE Intermembrane space Inner membrane Matrix Thylakoid space Thylakoid membrane Stroma Electron transport chain HH Diffusion ATP synthase HH ADP  P i KeyHigher [H  ] Lower [H  ] ATP Figure 10.17

62. 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 H 2 O to NADPH

63. Figure 10.18 STROMA (low H  concentration) THYLAKOID SPACE (high H  concentration) Light Photosystem II Cytochrome complex Photosystem I Light NADP  reductase NADP  + H  To Calvin Cycle ATP synthase Thylakoid membrane 2 13 NADPH Fd Pc Pq 4 H + +2 H + H+H+ ADP + P i ATP 1/21/2 H2OH2O O2O2

64. 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 The cycle builds sugar from smaller molecules by using ATP and the reducing power of electrons carried by NADPH

65. Carbon enters the cycle as CO 2 and leaves as a sugar named glyceraldehyde 3-phospate (G3P) For net synthesis of 1 G3P, the cycle must take place three times, fixing 3 molecules of CO 2 The Calvin cycle has three phases –Carbon fixation (catalyzed by rubisco) –Reduction –Regeneration of the CO 2 acceptor (RuBP)

66. Input 3 (Entering one at a time) CO 2 Phase 1: Carbon fixation Rubisco 3PP P6 Short-lived intermediate 3-Phosphoglycerate 3P P Ribulose bisphosphate (RuBP) Figure 10.19-1

67. Input 3 (Entering one at a time) CO 2 Phase 1: Carbon fixation Rubisco 3PP P6 Short-lived intermediate 3-Phosphoglycerate 6 6 ADP ATP 6PP 1,3-Bisphosphoglycerate Calvin Cycle 6 NADPH 6 NADP  6 P i6 P i 6P Phase 2: Reduction Glyceraldehyde 3-phosphate (G3P) 3P P Ribulose bisphosphate (RuBP) 1P G3P (a sugar) Output Glucose and other organic compounds Figure 10.19-2

68. Input 3 (Entering one at a time) CO 2 Phase 1: Carbon fixation Rubisco 3PP P6 Short-lived intermediate 3-Phosphoglycerate 6 6 ADP ATP 6PP 1,3-Bisphosphoglycerate Calvin Cycle 6 NADPH 6 NADP  6 P i6 P i 6P Phase 2: Reduction Glyceraldehyde 3-phosphate (G3P) P 5 G3P ATP 3 ADP Phase 3: Regeneration of the CO 2 acceptor (RuBP) 3P P Ribulose bisphosphate (RuBP) 1P G3P (a sugar) Output Glucose and other organic compounds 3 Figure 10.19-3

69. 4: Alternative mechanisms of carbon fixation have evolved in hot, arid climates Dehydration is a problem for 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

70. Photorespiration: An Evolutionary Relic? 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 consumes O 2 and organic fuel and releases CO 2 without producing ATP or sugar

71. 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 In many plants, photorespiration is a problem because on a hot, dry day it can drain as much as 50% of the carbon fixed by the Calvin cycle

72. C 4 Plants C 4 plants minimize the cost of photorespiration by incorporating CO 2 into four-carbon compounds in mesophyll cells This step requires the enzyme PEP carboxylase PEP carboxylase has a higher affinity for CO 2 than rubisco does; it can fix CO 2 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

73. Figure 10.20 C 4 leaf anatomy The C 4 pathway Photosynthetic cells of C 4 plant leaf Mesophyll cell Bundle- sheath cell Vein (vascular tissue) Stoma Mesophyll cell PEP carboxylase CO 2 Oxaloacetate (4C) PEP (3C) Malate (4C) Pyruvate (3C) CO 2 Bundle- sheath cell Calvin Cycle Sugar Vascular tissue ADP ATP

74. Figure 10.20a C 4 leaf anatomy Photosynthetic cells of C 4 plant leaf Mesophyll cell Bundle- sheath cell Vein (vascular tissue) Stoma

75. Figure 10.20b The C 4 pathway Mesophyll cell PEP carboxylase CO 2 Oxaloacetate (4C) PEP (3C) Malate (4C) Pyruvate (3C) CO 2 Bundle- sheath cell Calvin Cycle Sugar Vascular tissue ADP ATP

76. In the last 150 years since the Industrial Revolution, CO 2 levels have risen greatly Increasing levels of CO 2 may affect C 3 and C 4 plants differently, perhaps changing the relative abundance of these species The effects of such changes are unpredictable and a cause for concern

77. CAM Plants Some plants, including 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

78. Sugarcane Mesophyll cell Bundle- sheath cell C4C4 CO 2 Organic acid CO 2 Calvin Cycle Sugar (a) Spatial separation of steps (b) Temporal separation of steps CO 2 Organic acid CO 2 Calvin Cycle Sugar Day Night CAM Pineapple CO 2 incorporated (carbon fixation) CO 2 released to the Calvin cycle 21 Figure 10.21

79. Figure 10.21a Sugarcane

80. Figure 10.21b Pineapple

81. 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 structures such as roots, tubers, seeds, and fruits In addition to food production, photosynthesis produces the O 2 in our atmosphere

82. Light Light Reactions: Photosystem II Electron transport chain Photosystem I Electron transport chain NADP  ADP + P i RuBP ATP NADPH 3-Phosphoglycerate Calvin Cycle G3P Starch (storage) Sucrose (export) Chloroplast H2OH2O CO 2 O2O2 Figure 10.22