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chloroplasts and mitochondria form an energy circle
-photosynthesis uses prod of respiration (CO2 and H2O) as starting substrates
-respiration uses products of photosynthesis (organic molecules and oxygen) as starting substrates
chloroplasts
-triple membrane structure
-contain an outer membrane which interacts w/ cytosol and an inner membrane that encloses an internal compartment (stroma)
-stroma contains thylakoid disks that are stacked in columns called grana. thylakoid membrane separate the stroma from the interior of the thylakoid (lumen)
-thylakoid membrane contains chlorophyll that allow chloroplasts to capture light energy as well as protein complexes that convert light to chem energy
light dependent reactions
*use photosystems to capture energy from sunlight and use that energy to prod ATP and reduce the electron carrier NADP+ to NADPH
-require light
-occur in thylakoid
-prod O2 as byprod
-essential to respiration
light independent reactions
-carbon fixation and calvin cycle
-doesn’t require light
-occur in stroma
-use ATP and NADPH to synthesize organic molecules from CO2 through carbon fixation
photons
particle of light that acts as discrete bundle of energy
pigments absorb photons of visible light
-energy is inversely proportional to the wavelength of light
-thus, a photon of blue light (short wavelength) will have more energy than a photon of red light at the longer wavelength end
photoelectric effect
-if harnessed correctly the energy contained in light is able to remove electrons from some molecules
-when a photon strikes a molecule w the correct amount of energy then the molecule will absorb the photon and raise an electron to a higher energy level, leading to excited electrons
-during photosynthesis, the pigments in the chloroplasts act as photoelectric devices (absorb sunlight, excite electrons, and transfer them to an electron carrier)
chlorophyll a
-main pigment in plants
-absorbs violet-blue and red light
-only pigment that can directly convert light energy to chem energy
chlorophyll b
-accessory pigment
-absorbs blue and green light
-adds to range of absorbed light
-also function as anti-oxidants
photosystems
-light is captured by photosystems (pigments/proteins attached to the surface of a photosynthetic membrane
-consists of 2 linked components, an antenna complex and a reaction center
-in plants, H2O is the electron donor: it replaces electrons that reaction center donated to electron acceptor
antenna complex
hundreds of accessory pigment molecules gather photons and feed the captured light energy to the reaction center
reaction center
one or more chlorophyll a molecules passes excited electrons out of photosystem to drive ATP/organic molecule synthesis
chloroplasts have 2 linked photosystems
-2 photosystems carry out oxygenic photosynthesis (oxygen generating) through phosphorylation
-prod of NADPH from NADP+ and ATP from ADP
diagram of the light dependent reactions
*proton gradient is noly created by the activity of b6f complex, but also bc of the creation of protons through oxidation of water in P1 and loss of protons on the stromal side by the generation of NADPH
-proton gradient= potential energy that can be converted to chem energy (ATP) driven by ATP synthase
ATP is prod via chemiosmosis
-as the protons move down their concentration gradient from the thylakoid space to the stroma, ATP is synthesized from stroma from ATP and inorganic phosphate
-ATP synthase uses proton gradient to provide energy for ATP synthesis (like the ATP synthase in the mitochondrial inner membrane)
non cyclic phosphorylation
generates NADPH+ and ATP but building organic molecules requires more energy that this process can create
cyclic phosphorylation
-cyclic phosphorylation allows cells to producse additional ATP by “short circuiting” P1 to create larger proton gradient
-cells switch btwn noncyclic and cyclic phosphorylation as needed
calvin cycle
-biochem pathway that allows for carbon fixation
uses ATP as energy source
uses NADPH as source for protons and electrons
converts inorganic CO2 into organic carbs
also called C3 photosynthesis
-uses prod of light dependent reactions, ATP, and protons/electrons from NADPH
3 phases of CC
-carbon fixation
key step: attachment of CO2 to 5C sugar, ribulose 1-5 biphosphate (RuBP). subsequently used to generate 2 molecules of PGA
uses enzyme rubisco
-reduction
PGA reduced to G3P
-regeneration of RuBP
G3P used to regenerate RuBP
*input of 3 CO2 molecules prod G3P
*6 turns make enough C for a glucose molecule
glucose prod
-glucose is NOT a direct prod of CC (G3P is)
-2 molecules of G3P leave CC for every 6 molecules of CO2 fixed by CC
-each G3P contains 3 C (from 6 CO2)
-2 G3P used to prod 1 glucose in reactions in cytoplasm (2 G3P prod 1 6-C glucose)
-new glucose may be converted to sucrose/starch
photorespiration
-another metabolic reaction that the enzyme rubisco participates in
-rubisco has 2 enzymatic activities:
carboxylation
oxidation
-CO2 and O2 compete for active site on rubisco
-problem for C3 plants
carboxylation
-leads to carbon fixation
-addition of CO2 to RuBP
-favored under normal conditions
oxidation
-leads to photorespiration (reverses carbon fixation)
-addition of O2 to RuBP leads to CO2 release
-favored in hot/dry conditions (low CO2 and high O2 conditions)
climate influences photorespiration
-under normal conditions at 25% C, 20% of fixed carbon is lost to phosphorylation (bc rate of carboxylation is 4x that of oxidation)
-loss becomes greater as temp inc under hot, arid conditions
C4 and CAM pathways minimize photorespiration
-some plants have evolved to capture CO2 by another mechanism (C4 and CAM)
-add CO2 to pep carboxalase to form a 4-C molecule
use pep instead of rubisco
has a greater affinity for CO2 and no oxidase activity
-C4 plants use a spatial solution to separate C3 and C4 pathways to different cells
-CAM plants use a time based solution (temporarily sep C4 reactions which occur in the night from C3 reactions that occur during the day)
the C4 plants
-corn, sorghum, sugarcane
-fix carbon internally using pep in mesophyll cells
-malate is transported to bundle sheath cells, where pyruvate and CO is prod
-CO2 enters CC, carbon fixation by rubisco and CC
-pyruvate returns to mesophyll cells to reform pep and restart the cycle
-although C4 path reduces CO2 loss due to photorespiration, C4 pathway has a cost
requires 12 extra ATP compared to CC to make 1 glucose
CAM pathway
-many succulent plants like cacti
-stomata open during night (cool temp) and close during day
reverse of most plants
-fix CO2 using PEP during the night and store in vacuole
-when stomata close during the day, CO2 is released from vacuoles
-high levels of CO2 drive CC and minimize photorespiration