The process that converts light energy to the chemical energy of food
Occurs in the chloroplast of plant cells
Why it occurs: to convert light energy to chemical energy stored in glucose
Contains an inner and outer membrane
Stroma - dense fluid
Thylakoids - interconnected membrane sacs that separates the stroma from the interior thylakoids
Stacked thylakoids are called grana
Contains chlorophyll
Made of a parphyrin ring (A light-absorbing head) and a hydrocarbon tail that anchors the chlorophyll
Formula - CO2 + H2O + Light Energy = O2 + C6H12O6
O2 is derived from H2O
Chloroplasts splits H2O into Hydrogen and Oxygen
The convertion of solar energy to chemical energy in the form of ATP and NADPH
Wavelength = 380 (Purple) to 750 (red) nm
Light acts as a particle called photons that contain a fixed amoung of energy
Shorter wavelength = more energy
The color we see is the colour that is NOT absorbed by the pigment, but its absorbed
In chloroplasts, chlorophyll absorbs violet-blue and red, and reflects green
When molecule absorbs a photon, electrons get excited and jump from its ground state (low energy state) to an excited state (high energy state). They jump to a higher orbit level
Electron goes back down by losing energy, becoming released as heat
In Chlorophyll a, it absorbs best in red (662 nm) and blue (430 nm). It is NOT best in green
Reaction Center Complex - Special pair of chlorophyll a molecules and a molecule that accepts electrons to be reduced by the primary electron acceptor
Antenna complex - Has pigment molecules that boud to proteins
Photosystem II: Clorophyll a - P680 (Absorbed at 680 nm)
Photosystem I: Chlorophyll a - P700 (Absorbed at 700 nm)
Electrons flow from water to PSII, then to PSI to NADP+ (Comes from the splitting of water)
PSII absorbs a photon of light that strikes a pigment molecule that boosts the electrons. Electrons reach P680 which makes electrons excited, later transferred to the primary electron acceptor.
2 P680 - 2 P680+
A Z protein splits water, releasing oxygen
The photo-excited electrons passes from the primary electron acceptor to PSI via Electron Transport Chain (Plastoquinone, cytochrom complex, plastocyanin)
Electrons fall to a lower energy level for the synthesis of ATP
Noncylic phosphorylation - process of ATP synthesis
Photon strikes a pigment molecule of PSI, boosting electron to a higher energy level by reaching P700
2 P700 - 2 P700+ (Now an oxidizing agent)
Primary electron acceptor passes electron down a second ETC (Ferredoxin) that does NOT have a proton gradient (No ATP is made). NADPH is made from NADP+ Reductase
NADP+ + 2H+ = NADPH + H+
Electron transport from PSI to Ferredoxin is NOT allowed by the electron donation to NADP+ Reductase
The reduced Ferredoxin donates the electron back to Plastoquinone (Continually reduced and oxidized, moves protons accross the membrane)
PSI works independently
Net Result: Energy from light is converted to ATP without the oxidation of H2O or the reduction of NADP+ to NADPH
This helps meet the demand for ATP
Occurs when a plant has enought NADPH but still needs ATP
Uses ATP and NADPH to convert CO2 to sugar (G3P)
Anabolic process
ATP is used as an energy source, NADPH is used as a reducing agent
One glucose molecule = six cycles
Three cycles = 1 G3P
Carbon Fixation - CO2 attaches to Rubilose Bisphosphate (RuBP 5C), becoming catalyzed by rubisco. The product made gets splits in half to form two molecules of 3-Phosphoglycerate
Reduction - 3-Phosphoglycerate receives a phosphate group from ATP making 1, 3-Bisphosphoglycerate. This gets reduced by NADPH to form Glyceraldehyde-3-phosphate (G3P). Reduction results in the loss of a phosphate group
3 CO2 = 1 G3P
Six molecules of G3P are made (18C) after fixation and reduction
Five are used for the regeneration of three RuBP
Regeneration - Carbon skeletons of 5 G3P are rearranged into 3 RuBP. Three more molecules of ATP are catabolized to also regenerate RuBP
Light reactions and Clavin cycle are physically separated, making O2 unexposed
Uses a C4 cycle that feeds CO2 to rubisco
Also has a C4 Cycle but biochemichal pathways aren’t separated
Opens stomata at night, allowing CO2 to enter & minimize H2O loss
CO2 is converted to make malate, which gets stored until daytime