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How Cells Acquire Energy Photosynthesis. Chapter 6a. Carbon and Energy Sources. Photoautotrophs Carbon source is carbon dioxide Energy source is sunlight Heterotrophs Get carbon and energy by eating autotrophs or one another. Photoautotrophs .
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How Cells Acquire EnergyPhotosynthesis Chapter 6a
Carbon and Energy Sources • Photoautotrophs • Carbon source is carbon dioxide • Energy source is sunlight • Heterotrophs • Get carbon and energy by eating autotrophs or one another
Photoautotrophs • Capture sunlight energy and use it to carry out photosynthesis • Plants • Some bacteria • Many protista
T.E. Englemann’s Experiment Background • Certain bacterial cells will move toward places where oxygen concentration is high • Photosynthesis produces oxygen
T.E. Englemann’s Experiment Hypothesis • Movement of bacteria can be used to determine optimal light wavelengths for photosynthesis
T.E. Englemann’s Experiment Method • Algal strand placed on microscope slide and illuminated by light of varying wavelengths • Oxygen-requiring bacteria placed on same slide
T.E. Englemann’s Experiment Results Bacteria congregated where red and violet wavelengths illuminated alga Conclusion Bacteria moved to where algal cells released more oxygen--areas illuminated by the most effective light for photosynthesis
Photosynthesis Energy-storing pathway Releases oxygen Requires carbon dioxide Aerobic Respiration Energy-releasing pathway Requires oxygen Releases carbon dioxide Linked Processes
Chloroplasts Organelles of photosynthesis
Photosynthesis Equation LIGHT ENERGY 6O2 + C6H12O6 + 6H2O 12H2O + 6CO2 oxygen glucose water carbon dioxide water
Two Stages of Photosynthesis sunlight water uptake carbon dioxide uptake ATP ADP + Pi LIGHT DEPENDENT-REACTIONS LIGHT INDEPENDENT-REACTIONS NADPH NADP+ glucose P oxygen release new water
Sunlight Energy • Continual input of solar energy into Earth’s atmosphere • Almost 1/3 is reflected back into space • Of the energy that reaches Earth’s surface, about 1% is intercepted by photoautotrophs
Electromagnetic Spectrum Shortest Gamma rays wavelength X-rays UV radiation Visible light Infrared radiation Microwaves Longest Radio waves wavelength
Visible Light • Wavelengths humans perceive as different colors • Violet (380 nm) to red (750 nm) • Longer wavelengths, lower energy
Photons • Packets of light energy • Each type of photon has fixed amount of energy • Photons having most energy travel as shortest wavelength (blue-green light)
Pigments • Light-absorbing molecules • Absorb some wavelengths and transmit others • Color you see are the wavelengths NOT absorbed chlorophyll a chlorophyll b Wavelength (nanometers)
Pigment Structure • Light-catching part of molecule often has alternating single and double bonds • These bonds contain electrons that are capable of being moved to higher energy levels by absorbing light
Excitation of Electrons • Excitation occurs only when the quantity of energy in an incoming photon matches the amount of energy necessary to boost the electrons of that specific pigment • Amount of energy needed varies among pigment molecules
Variety of Pigments Chlorophylls a and b Carotenoids Anthocyanins Phycobilins
Chlorophylls Main pigments in most photoautotrophs chlorophyll a Wavelength absorption (%) chlorophyll b Wavelength (nanometers)
Carotenoids • Found in all photoautotrophs • Absorb blue-violet and blue-green that chlorophylls miss • Reflect red, yellow, orange wavelengths • Two types • Carotenes - pure hydrocarbons • Xanthophylls - contain oxygen
Anthocyanins & Phycobilins Red to purple pigments • Anthocyanins • Give many flowers their colors • Phycobilins • Found in red algae and cyanobacteria
Pigments in Photosynthesis • Bacteria • Pigments in plasma membranes • Plants • Pigments embedded in thylakoid membrane system • Pigments and proteins organized into photosystems • Photosystems located next to electron transport systems
Photosystems and Electron Transporters water-splitting complex thylakoid compartment H2O 2H + 1/2O2 P680 P700 acceptor acceptor PHOTOSYSTEM II pool of electron transporters stroma PHOTOSYSTEM I
Light-Dependent Reactions • Pigments absorb light energy, give up e- which enter electron transport systems • Water molecules are split, ATP and NADH are formed, and oxygen is released • Pigments that gave up electrons get replacements from the splitting of H2O
Photosystem Function: Harvester Pigments • Most pigments in photosystem are harvester pigments • When excited by light energy, these pigments transfer energy to adjacent pigment molecules • Each transfer involves energy loss
Photosystem Function: Reaction Center • Energy is reduced to level that can be captured by a special molecule of chlorophyll a • This molecule (P700 or P680) is the reaction center of a photosystem • Reaction center accepts energy and donates electron to acceptor molecule
Pigments in a Photosystem reaction center (a specialized chlorophyll a molecule)
Electron Transport System • Adjacent to photosystem • Acceptor molecule donates electrons from reaction center to the system • As electrons flow through system, the energy they release is used to produce ATP and, in some cases, NADPH
Cyclic Electron Flow • Electrons • are donated by P700 in photosystem I to acceptor molecule • flow through electron transport system and back to P700 via a soluble protein carrier • Electron flow drives ATP formation • No NADPH is formed
Cyclic Electron Flow e– electron acceptor electron transport system e– e– ATP e–
Noncyclic Electron Flow • Two-step pathway for light absorption and electron excitation • Uses two photosystems: type I and type II • Produces ATP and NADPH • Involves photolysis - splitting of water
Pigments in a Photosystem reaction center (a specialized chlorophyll a molecule)
Machinery of Noncyclic Electron Flow H2O photolysis PCH2 PC e– Ferredoxin PQ PQH2 ATP SYNTHASE Cytochrome b/ f complex e– NADP+ NADPH ATP PHOTOSYSTEM II PHOTOSYSTEM I ADP + Pi
Energy Changes second transport system e– NADPH e– first transport system e– Potential to transfer energy (voids) e– (PHOTOSYSTEM I) (PHOTOSYSTEM II) 1/2 O2 + 2H+ H2O
Chemiosmotic Model of ATP Formation • When water is split during photolysis, hydrogen ions are released into thylakoid compartment • More hydrogen ions are pumped into the thylakoid compartment when the electron transport system operates
Chemiosmotic Model of ATP Formation • Electrical and H+concentration gradients exist between thylakoid compartment and stroma • H+ flows down gradients into stroma through a channel in an integral thylakoid membrane protein, ATP synthetase • Flow of ions drives formation of ATP
Light-Independent Reactions • Synthesis part of photosynthesis • Can proceed in the dark • Take place in the stroma • Calvin-Benson cycle
Overall reactants Carbon dioxide ATP NADPH Overall products Glucose ADP NADP+ Calvin-Benson Cycle Reaction pathway is cyclic and RuBP (ribulose bisphosphate) is regenerated
6 CO2 (from the air) Calvin- Benson Cycle CARBON FIXATION 6 6 RuBP unstable intermediate 12 PGA 6 ADP 12 ATP 6 ATP 12 NADPH 4 Pi 12 ADP 12 Pi 12NADP+ 10 PGAL 12 PGAL 2 PGAL Pi P glucose
Building Glucose • PGA accepts • phosphate from ATP • hydrogen and electrons from NADPH • PGAL (phosphoglyceraldehyde) forms • When 12 PGAL have formed • 10 are used to regenerate RuBP • 2 combine to form phosphorylated glucose
Using the Products of Photosynthesis • Phosphorylated glucose is the building block for: • sucrose • The most easily transported plant carbohydrate • starch • The most common storage form
The C3 Pathway • In Calvin-Benson cycle, the first stable intermediate is a three-carbon PGA • Because the first intermediate has three carbons, the pathway is called the C3 pathway
Photorespiration in C3 Plants • On hot, dry days stomata close • Inside leaf • Oxygen levels rise • Carbon dioxide levels drop • Rubisco attaches RuBP to oxygen instead of carbon dioxide • Only one PGAL forms instead of two plus one glycolate ( OH-CH2-COOH)
C4 Plants • Carbon dioxide is fixed twice • In mesophyll cells, carbon dioxide is fixed by PEP to form four-carbon oxaloacetate • Oxaloacetate is reduced to malate, which is then transferred to bundle-sheath cells • Carbon dioxide is released from malate and fixed again in Calvin-Benson cycle
CAM Plants • Carbon is fixed twice (in same cells) • Night • Carbon dioxide is fixed as C4 organic acids • Day • Fixed Carbon dioxide released from C4 acids is fixed again by ribulose biphosphate in Calvin-Benson cycle
CO2or O2 CO2+ H2O Inmesophyll cell, Rubisco affixes O2 to RibuloseBP. CO2 One glycolate and only one PGA (not two) lower CO2 uptake, fewer sugars can form CALVIN- BENSON CYCLE ATP+ Pyruvate + PEP (phosphoenolpyruvate) Oxaloacetate in mesophyll cell, cell carbon fixation Malate C3 PLANTS. With low CO2 / high O2, photorespiration predominates. - Malate Pyruvate + CO2 . CO2 in bundle-sheath cell, carbon is fixed again more CO2 in leaf; no photorespiration (See next slide.) At night CO2 is high & O2 low . In mesophyll cells, stomata open at night; CO2 uptake but no water loss CALVIN- BENSON CYCLE CO2 CO2 PEP + CO2 C4 C4 PLANTS. With low CO2 / high O2, Calvin-Benson cycle predominates during the hot day (stomata are closed to preserve water). CO2 + C3 Stomata close during day;CO2 is low. Fixed CO2 that accumulated overnight as C4 in leaf is used during day by Calvin Benson cycle. CALVIN- BENSON CYCLE Fig. 6.15, p. 102 CAM PLANTS. With low CO2 / high O2, Calvin-Benson cycle predominates.
Hydrothermal Vents • Fissures in sea-floor where seawater mixes with molten rock • Complex ecosystem is based on energy from these vents • Bacteria are producers in this system
Light and Life at the Vents • Vents release faint radiation at low end of visible spectrum • These photons could be used to carry out photosynthesis • Nisbet and Van Dover hypothesize that the first cells may have arisen at hydrothermal vent systems