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Published byLoren McKinney Modified over 9 years ago
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CHAPTER 10
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stomata – pores in lower epidermis of leaf gas exchange mesophyll – inner-leaf tissue most chloroplasts located in these cells veins (phloem & xylem) phloem carries sugars away from leaves xylem carries water to leaves
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stroma – inner fluid thylakoids – interconnected membranous sacs contains chlorophyll grana – stacks of thylakoids
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involves redox reactions 2 stages: light reactions – convert solar energy to chemical energy stored temporarily in ATP & NADPH Calvin cycle – conversion of CO 2 into glucose using the energy stored in ATP & NADPH 6 CO 2 + 6 H 2 O + light energy C 6 H 12 O 6 + 6 O 2
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a mixture of wavelengths 380-750 nm when passed thru a prism, separates into the colors of the rainbow
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absorb visible light some wavelengths (colors of light) are not absorbed but reflected or transmitted– this is the color we see (ex) leaves look green because the pigment chlorophyll reflects and transmits green light
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a machine that determines the wavelengths of light absorbed by a pigment by measuring the percent transmittance of each color of light allows us to create an absorption spectrum
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chlorophyll a absorbs blue-violet & red light best chlorophyll b absorbs blue & orange light best
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pigments become excited when they absorb light because absorption of a photon of light boosts an electron to a higher energy level if the energy is not captured, the electrons will quickly fall back to their ground state & the energy is released as heat sometimes light is also emitted as the electrons fall back down to their ground state – the resulting after- glow is called fluorescence
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light-harvesting complexes in the thylakoid membranes consisting of pigment molecules bound to proteins two types: photosystem II (P680) & photosystem I (P700) create a greater surface area for absorbing light increase the range of wavelengths that can be absorbed by the plant (due to presence of chlorophyll a, chlorophyll b, and carotenoids) have two parts: reaction center (chlorophyll a + primary electron acceptor) surrounded by light- harvesting complexes
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light strikes pigment molecules in light- harvesting complexes energy is passed from one pigment molecule to another until it reaches chlorophyll a in the reaction center this excites an electron in chlorophyll a which is picked up by the primary electron acceptor
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non-cyclic electron flow flow of electrons from PS II PS I NADP + produces ATP and NADPH for the Calvin cycle cyclic electron flow cycling of electrons within PS I; does not involve PS II produces additional ATP needed for Calvin cycle NADPH concentration regulates which type occurs high [NADPH] stimulates cyclic electron flow to balance out NADPH & ATP levels
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ATP is made during the light reactions using the same process (chemiosmosis) that makes ATP during oxidative phosphorylation of cellular respiration
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light strikes PS II causing electrons in chlorophyll a in the reaction center to become excited the excited electrons are picked up by the primary electron acceptor & passed down an electron transport chain which drives the synthesis of ATP by chemiosmosis meanwhile, light strikes PS I causing electrons in chlorophyll a in the reaction center to become excited the excited electrons are picked up by the primary electron acceptor & passed down an electron transport chain to NADP + which is reduced to NADPH
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the electrons lost from the chlorophyll a molecules in each photosystem are restored as follows: electrons are restored to PS II by the splitting of H 2 O which produces O 2 as a by-product electrons are restored to PS I by the electron transport chain that follows PSII (PS I is the final electron acceptor for this ETC) cont.
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carbon fixation – CO 2 is attached to a molecule called RuBP by the enzyme rubisco forming an unstable six-carbon compound that immediately splits into two three-carbon compounds called 3- PGA ATP & NADPH drive the conversion of 3-PGA to G3P for every three CO 2 that enter the cycle, six G3P are made – one leaves the cycle and five are recycled to regenerate RuBP (requires ATP) glucose is made from the G3P that leaves the Calvin cycle
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plants that perform the steps of photosynthesis previously discussed are called C 3 plants C 3 plants use CO 2 directly from the air by opening their stomata this can be a problem on hot, dry days when plants close their stomata to reduce water loss because when stomata are closed, no CO 2 can enter the leaf & no O 2 can get out the O 2 build-up causes photorespiration, a process in which rubisco adds O 2 to RuBP in the Calvin cycle instead of CO 2 photorespiration does not produce glucose like photosynthesis or ATP like cellular respiration so it is basically a wasteful process
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C4 photosynthesis PEP carboxylase (which has a higher affinity for CO 2 than rubisco & no affinity for O 2 ) combines CO 2 with PEP to make oxaloacetate which is converted to malate and stored in the bundle-sheath cells CO 2 is released in the bundle-sheath cells and enters the Calvin cycle this adaptation is used in hot regions with intense sunlight where stomata partially close during the day examples of plants that use this adaptation are corn & sugarcane
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CAM photosynthesis plants take in CO 2 at night and store it in organic acids CO 2 is released during the day for use in the Calvin cycle when light is available for the light reactions this adaptation is used by plants that live in extremely arid environments like deserts examples of plants that use this adaptation are cacti, pineapples, & succulents (water-storing plants) cont.
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C4 PHOTOSYNTHESISCAM PHOTOSYNTHESIS spatial separation of steps temporal separation of steps
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