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Chapter 22. Photosynthesis to accompany Biochemistry, 2/e by Reginald Garrett and Charles Grisham.
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Chapter 22 Photosynthesis to accompany Biochemistry, 2/e by Reginald Garrett and Charles Grisham All rights reserved. Requests for permission to make copies of any part of the work should be mailed to: Permissions Department, Harcourt Brace & Company, 6277 Sea Harbor Drive, Orlando, Florida 32887-6777
Outline • 22.2 The Photoreactivity of Chlorophyll • 22.4 The Z Scheme of Photosynthesis • 22.7 Light-Driven ATP Synthesis - Photophosphorylation • 22.8 Carbon Dioxide Fixation • 22.9 The Calvin-Benson Cycle • 22.10 Regulation of Carbon Dioxide Fixation • 22.12 The C-4 Pathway of CO2 Fixation
The Sun - Ultimate Energy 1.5 x 1022 kJ falls on the earth each day • 1% is absorbed by photosynthetic organisms and transformed into chemical energy • 6CO2 + 6H2O C6H12O6 + 6O2 • 1011 tons (!) of CO2 are fixed globally per year • Formation of sugar from CO2 and water requires energy • Sunlight is the energy source!
Photosynthesis General Aspects • Photosynthesis occurs in thylakoid membranes of chloroplasts - structures involving paired folds (lamellae) that stack to form "grana" • The soluble portion of the chloroplast is the "stroma" • The interior of the thylakoid vesicles is the "thylakoid space" or "thylakoid lumen" • Chloroplasts possess DNA, RNA and ribosomes
Photosynthesis Consists of Both Light Reactions and Dark Reactions • The light reactions capture light energy and convert it to chemical energy in the form of reducing potential (NADPH) and ATP with evolution of oxygen • The dark reactions use NADPH and ATP to drive the endergonic process of hexose sugar formation from CO2 in a series of reactions in the stroma
Water is the electron donor for Photosynthetic NADP+ Reduction • Equations 22.2 and 22.3 describe the light and dark reactions in green plants, respectively! • Equation 22.4 provides a more general version • Photosynthetic bacteria use H2S, isopropanol or other oxidizable substrates • The O2 we depend upon depends in turn on large amounts of photosynthesis on the earth!
Chlorophyll Photoreactive, isoprene-based pigment • A planar, conjugated ring system - similar to porphyrins • Mg in place of iron in the center • Long chain phytol group confers membrane solubility • Aromaticity makes chlorophyll an efficient absorber of light
The Photosynthetic Unit Many chlorophylls but only a single reaction center • The "unit" consists of several hundred light-capturing chlorophylls plus a pair of special chlorophylls in the "reaction center" • Light is captured by one of the "antenna chlorophylls" and routed from one to the other until it reaches the reaction center • See Figure 22.9
Eukaryotic Photosystems PSI (P700) and PSII (P680) • All chlorophyll is part of either LHC, PSI or PSII • PSI absorbs at 700 nm • PSII absorbs at 680 nm • Chloroplasts given light at 680 and 700 nm simultaneously yield more O2 than the sum of amounts when each is used alone.
What does each photosystem do? See Figure 22.11 • PSII oxidizes water (termed “photolysis") • PSI reduces NADP+ • ATP is generated by establishment of a proton gradient as electrons flow from PSII to PSI
The Z Scheme An arrangement of the electron carriers as a chain according to their standard reduction potentials • PQ = plastoquinone • PC = plastocyanin • "F"s = ferredoxins • Ao = a special chlorophyll a • A1 = a special PSI quinone • Cytochrome b6/cytochrome f complex is a proton pump
Oxygen evolution by PSII requires accumulation of four oxidizing equivalents • PSII (P680) cycles through five oxidation states • 1 e- is removed in each of four steps • Fifth step involves H2O oxidized to O2 + 4H+
Structures of Reaction Centers R. viridis is a model! • Membrane proteins (as always) are resistant to crystallization (and X-ray diffraction studies) • Deisenhofer, Michel and Huber solved R.viridis structure in 1984 (Nobel Prize same year!) • Four peptides: L, M, H and cytochrome • No electron transfer appears to occur through M • See Figures 22.16, 22.18
The Quantum Yield Amount of O2 evolved per photon • Four photons per reaction center - 8 total - drive the evolution of 1 O2, reduction of 2 NADP+, and the phosphorylation of 2 and 2/3 ATP
Photophosphorylation Light-Driven ATP Synthesis • Electron transfer through the proteins of the Z scheme drives the generation of a proton gradient across the thylakoid membrane • Protons pumped into the lumen of the thylakoids flow back out, driving the synthesis of ATP • CF1-CFo ATP synthase is similar to the mitochondrial ATP synthase
Cyclic Photophosphorylation ATP without NADPH! • The photo-excited electron removed from P700 returns to P700 in a pathway indicated by the dashed line in Figure 22.12 • Cyclic photophosphorylation depends only on PSI, not on PSII
Carbon Dioxide Fixation A unique ability of plants, algae, etc. • Melvin Calvin at Berkeley in 1945 showed that Chlorella could take up 14CO2 and produce 3-phosphoglycerate • What was actually happening was that CO2 was combining with a 5-C sugar to form a 6-C intermediate • This breaks down to two 3-P glycerates
Ribulose-1,5-Bisphosphate The CO2 Acceptor • Fixation is accomplished by ribulose bisphosphate carboxylase (oxygenase), aka rubisco • Probably the world's most abundant protein • Study the mechanism in Figure 22.24 • Rubisco is activated when carbamylated (CO2 added to Lys-201) and with Mg bound • RuBP (substrate!) is inhibitor and must be released from inactive rubisco by rubisco activase. Carbamylation and Mg then activate.
The Calvin-Benson Cycle aka The Calvin Cycle • The set of reactions that transform 3-P- glycerate into hexose sugar • The only net CO2 fixation pathway in nature • A disguised gluconeogenesis pathway! • With some pentose phosphate pathway reactions thrown in.... • See Figure 22.25
Regulation of CO2 Fixation Activities of Calvin cycle enzymes (in the stroma!) are coordinated with photosynthesis • Three effects: • Light-induced pH changes • Light-induced generation of reducing power (reduced ferredoxin and NADPH) • Light-induced Mg2+ Efflux from Thylakoids
The C-4 Pathway for CO2 Fixation aka the Hatch-Slack Pathway • Not an alternative to Calvin cycle, nor even a net CO2 fixation pathway • Rather, it is a CO2 delivery system, which carries CO2 from the O2-rich leaf surface to interior cells where O2 won't compete in the rubisco reaction • Oxaloacetate and malate are the CO2 transporters • Read about Crassulacean acid metabolism