10. photosynthesis
plants and other photosynthetic organisms contain organelles called chloroplasts
photosynthesis is the process that converts solar energy into chemical energy within chloroplasts
carotenoids (the pigment) produces the red, orange and yellow colours in plant
directly or indirectly photosynthesis nourishes almost the entire living world
autotrophs - self-feeders that sustain themselves without eating anything derived from other organisms
producers of the biosphere, producing organic molecules from CO2 and other inorganic molecules
almost all plants are photoautotrophs, using the energy of sunlight to make organic molecules
photosynthesis occurs in plants, algae, certain other unicellular eukaryotes and some prokaryotes
heterotrophs - obtain organic material from other organisms
consumers of the biosphere
some eat other living organisms and others, decomposers, consume dead organic material or feces
almost all heterotrophs depend on photoautotrophs for food and O2
earth’s supply of fossil fuels was formed from the remains of organisms that died hundreds of millions of years ago
fossil fuels are being consumed faster than they are being replenished
researchers are exploring methods of using the photosynthetic process to produce alternative fuels
chloroplasts - structurally similar to and likely evolved from photosynthetic bacteria
the structural organization of these organelles allows for the chemical reactions of photosynthesis
leaves are the major locations of photosynthesis in plants
chloroplasts are found mainly in cells of the mesophyll (the interior tissue of the leaf)
each mesophyll cell contains 30-40 chloroplasts
CO2 enters and O2 exits the leaf through microscopic pores called stomata
a chloroplast has an envelope of 2 membranes surrounding a dense fluid called the stroma
thylakoids are connected sacs in the chloroplast that compose a third membrane system
lamella connects the thylakoids
chlorophyll, the pigment that gives leaves their green color, resides in the thylakoid membranes
photosynthesis is a complex series of reactions that can be summarized as the equation:
6CO2 + 12H2O + light energy → C6H12O6 + 6O2 + 6H2O
the overall chemical change during photosynthesis is the reverse of the one that occurs during cellular respiration
chloroplasts split H2O into hydrogen and oxygen, incorporating the electrons of hydrogen into sugar molecules and releasing oxygen as a by-product
photosynthesis reverses the direction of electron flow compared to respiration
photosynthesis is a redox reaction in which H2O is oxidized and CO2 is reduced
photosynthesis is an endergonic process where the energy boost is provided by light
photosynthesis consists of light reactions (the photo part) and the Calvin cycle (the synthesis part)
the light reaction occurs in the thylakoids
splits H2O
releases O2
reduces the electron acceptor NADP+ to NADPH
(functionally the same as NAD and NADH)
generates ATP from ADP by photophosphorylation
the Calvin cycle occurs in the stroma and forms sugar from CO2 using ATP and NADPH
begins with carbon fixation, incorporating CO2 into organic molecules
chloroplasts are solar-powered chemical factories
their thylakoids transform light energy into the chemical energy of ATP and NADPH
light is electromagnetic energy, also called electromagnetic radiation
electromagnetic energy travels in rhythmic waves
wavelength is the distance between crests of electromagnetic waves
wavelength determines the type of electromagnetic energy
the electromagnetic spectrum is the entire range of electromagnetic energy or radiation
visible light consists of wavelengths (370nm to 750 nm) that produce colors we can see
visible light also includes the wavelengths that drive photosynthesis
plants tend to like light on the ends of the spectrum (red or violet)
photon energy is used from those two ends of the spectrum
light also behaves as though it consists of discrete particles called photons
the majority of plants are green bc it uses everything but the green waves/photons so they get reflected back to us
in autumn, leaves are reddish orange because those photons provide less energy and since there is already not enough energy from the sun at that it, it will prefer using waves on the shorter sides ( more energy)
pigments are substances that absorb visible light
different pigments absorb different wavelengths
wavelengths that are not absorbed are reflected or transmitted
leaves appear green because chlorophyll reflects and transmits green light
a spectrophotometer measures a pigment’s ability to absorb various wavelengths
this machine sends light through pigments and measures the fraction of light transmitted at each wavelength
an absorption spectrum is a graph plotting a pigment’s light absorption versus wavelength
there are 3 types of pigments in chloroplasts
chlorophyll a - the key light-capturing pigment
chlorophyll b - tan accessory pigment
carotenoids, a separate group of accessory pigments
do not produce as much sugar as chlorophyll
a and b differ by a functional group
the action spectrum profiles the relative effectiveness of different wavelengths of radiation in driving a process
the action spectrum of photosynthesis was first demonstrated in 1883 by Theodor W. Engelmann
in his experiment, he exposed different segments of filamentous alga to different wavelengths
areas receiving wavelengths favorable to photosynthesis produced excess O2
he used the growth of aerobic bacteria clustered along the alga as a measure of O2 production
the action spectrum for photosynthesis is broader than the absorption spectrum of chlorophyll
accessory pigments such as chlorophyll b broaden the spectrum for photosynthesis
the difference in the absorption spectrum between chlorophyll a and b is due to a slight structural difference between the pigment molecules
in chlorophyll a - methyl group
in chlorophyll b - carbonyl group
porphyrin ring - light absorbing head of molecule with magnesium at the center
hydrocarbon tail - interacts with hydrophobic regions of proteins inside the thylakoid membranes of chloroplasts
magnesium in the middle gives off electrons when light hits it which travel to the other parts of the molecule (replenishing electrons come from H2O)
accessory pigments called carotenoids may broaden the spectrum of colors that drive photosynthesis
some carotenoids function in photoprotection; they absorb excessive light that would damage chlorophyll or react with oxygen
a photosystem consists of a reaction-center complex surrounded by light-harvesting complexes
the reaction-center complex is an association of proteins holding a special pair of chlorophyll a molecules and primary electron acceptors
the light harvesting complex consists of pigment molecules bound to proteins
light-harvesting complexes transfer the energy of photons to the chlorophyll a molecules in the reaction-center complex
these chlorophyll a molecules are special because they can transfer an excited electron to a different molecule
a primary electron acceptor in the reaction center accepts excited electrons and is reduced as a result
solar-powered transfer of an electron from a chlorophyll a molecule to the primary electron acceptor is the first step of the light reactions
there are 2 types of photosystems in the thylakoid membrane
photosystem II (PSII) functions first
the reaction-center chlorophyll a of PS II is called P680 because it is best at absorbing a wavelength of 680 nm
photosystem I (PSI) - is best at absorbing a wavelength of 700nm
the reaction-center chlorophyll a of PSI is called P700
during the light reactions, there are 2 possible routes for electron flow
cyclic - electrons get recycled
linear - electrons leave the system
linear electron flow - the primary pathway involves both photosystems and produces ATP and NADPH using light energy
there are 8 steps to linear electron flow:
a photon hits a pigment in a light-harvesting complex of PSII and its energy is passed among pigment molecules until it excites P680
an excited electron from P680 is transferred to the primary electron acceptor and becomes P680+
H2O is split by enzymes and the electrons are transferred from the hydrogen atoms to P680+ reducing it to P680
P680+ is the strongest known biological oxidizing agent (oxidizes water)
the H+ are released into the thylakoid space
O2 is released as a by-product of this reaction
each electron “falls” down an electron transport chain from the primary electron acceptor of PSII to PSI. Energy released by the fall drives the creation of a proton gradient across the thylakoid membrane
potential energy stored in the proton gradient drives production of ATP by chemiosmosis
in PSI, transferred light energy excites P700 which loses an electron to the primary electron acceptor
P700+ accepts an electron passed down from PSII via the electron transport chain
each electron “falls” down an electron transport chain from the primary electron acceptor of PSI to the protein ferredoxin (Fd)
NADP+ reductase catalyzes the transfer of electrons to NADP+, reducing it to NADPH
the electrons of NADPH are available for the reactions of the Calvin cycle
the process also removes an H+ from the stroma
the energy changes of electrons during linear flow through the light reactions can be shown in a mechanical analogy
in cyclic electron flow, electrons cycle back from Fd to the PSI reaction center via a plastocyanin molecule (PC)
cyclic electron flow uses only photosystem I and produces ATP but not NADPH
no oxygen is released
some organisms such as purple sulphur bacteria and cyanobacteria have PSI but not PSII
cyclic electron flow is thought to have evolved before linear electron flow
cyclic electron flow may protect cells from light-induced damage
chloroplasts and mitochondria generate ATP by chemiosmosis but use different sources of energy
mitochondria transfer chemical energy from food to ATP; chloroplasts transform light energy into the chemical energy of ATP
spatial organization of chemiosmosis differs between chloroplasts and mitochondria but shows similarities
in mitochondria, protons are pumped to the intermembrane space and drive ATP synthesis as they diffuse back into the mitochondrial matrix
in chloroplasts, protons are pumped into the thylakoid space and drive ATP synthesis as they diffuse back into the stroma
ATP and NADPH are produced on the side facing the stroma where the calvin cycle takes place
in summary, light reactions generate ATP and increase the potential energy of electrons by moving them from H2O to NADPH
the calvin cycle, like the krebs cycle regenerates its starting material after molecules enter and leave the cycle
the calvin cycle is anabolic; it builds sugar from smaller molecules by using ATP and the reducing power of electrons carried by NADPH
carbons enter the cycle as CO2 and leave as G3P
for net synthesis of one G3P, the cycle must take place 3 times, fixing 3 molecules of CO2
the calvin cycle has 3 phases
carbon fixation (catalyzed by rubisco)
adding carbon onto a molecule
reduction
regeneration of the CO2 acceptor (RuBP)
rubisco is an enzyme that performs carbon fixation on RuBP
ATP, ADP and NADPH are produced
must go through the cycle 6 times for one glucose molecule to be made
6 CO2 used per glucose
dehydration is a problem for plants, sometimes requiring trade-offs with other metabolic processes, especially photosynthesis
on hot, dry days, plants close their stomata which conserves H2O but also limits photosynthesis
plants will make ATP and NADH during the day
at night, stomata will open and take CO2 to do the calvin cycle
cacti are acidic because they store CO2 as organic acid
the closing of stomata reduces access to CO2 and causes O2 to build up
having a lot of O2 causes an apparently wasteful process called photorespiration
in most plants (C3 plants), initial fixation of CO2 via rubisco forms a 3-carbon compound called 3-phosphoglycerate
because rubisco is such an old enzyme, it cannot tell the difference between O2 and CO2
in photorespiration, rubisco adds O2 instead of CO2 in the calvin cycle, producing a 2-carbon compound
photorespiration consumes O2 and organic fuel and releases CO2 without producing ATP or sugar
causes the whole cell to shut down
photorespiration may be an evolutionary relic because rubisco evolved at a time where O2 barely existed
photorespiration limits damaging products of light reactions that build up in the absence of the calvin cycle
in many plants, photorespiration is a problem because on a hot, dry day, it can drain as much as 50% of the carbon fixed by the calvin cycle
C4 plants minimize the cost of photorespiration by incorporating CO2 into 4-carbon compounds
there are 2 distant types of cells in the leaves of C4 plants
bundle sheath cells - arranged in tightly packed sheaths around the veins of the leaf
mesophyll cells - loosely packed between the bundle sheath and the leaf surface
sugar production in C4 plants occur in a 3 step process
the production of the 4-carbon precursors is catalyzed by the enzyme PEP carboxylase in the mesophyll cells
PEP carboxylase has a higher affinity for CO2 than rubisco does; it can fix CO2 even when concentrations are low
the 4-carbon compounds are exported to bundle sheath cells
within the bundle-sheath cells, they release CO2 that is then used in the calvin cycle
PEP carboxylase fixes CO2 with pyruvate (3C) to make malic acid (4C)
in the C4 pathway, the PEP carboxylase and the calvin cycle occur in different cells to prevent the rubisco from having access to O2 (stops photorespiration)
since the industrial revolution in the 1800s, CO2 levels have risen greatly
increasing levels of CO2 may affect C3 and C4 plants differently, perhaps changing the relative abundance of these species
the effects of such changes are unpredictable and a cause for concern
suitable agricultural land is decreasing due to the effects of climate change, while the world demand for food continues to increase
C4 photosynthesis uses less water and resources than C3 photosynthesis
scientists have genetically modified rice, a C3 plant, to carry out C4 photosynthesis
they estimate 30-50% increase in yield compared to C3 rice
some plants including succulents use crassulacean acid metabolism (CAM) to fix carbon
CAM plants open their stomata at night, incorporating CO2 into organic acids that are stored in the vacuoles
like pineapples
stomata close during the day and CO2 is released from organic acids and used in the Calvin cycle
the CAM pathway is similar to the C4 pathway in that they both incorporate CO2 into organic intermediates before it enters the calvin cycle
in the CAM pathway, these steps occur in the same cell but are separated by time
the energy entering chloroplasts as sunlight gets stored as chemical energy in organic compounds
sugar made in the chloroplasts supplies chemical energy and carbon skeletons to synthesize the organic molecules of cells
plants store excess sugar as starch in chloroplasts and other structures such as roots, tuber, seeds and fruits
plants and other photosynthetic organisms contain organelles called chloroplasts
photosynthesis is the process that converts solar energy into chemical energy within chloroplasts
carotenoids (the pigment) produces the red, orange and yellow colours in plant
directly or indirectly photosynthesis nourishes almost the entire living world
autotrophs - self-feeders that sustain themselves without eating anything derived from other organisms
producers of the biosphere, producing organic molecules from CO2 and other inorganic molecules
almost all plants are photoautotrophs, using the energy of sunlight to make organic molecules
photosynthesis occurs in plants, algae, certain other unicellular eukaryotes and some prokaryotes
heterotrophs - obtain organic material from other organisms
consumers of the biosphere
some eat other living organisms and others, decomposers, consume dead organic material or feces
almost all heterotrophs depend on photoautotrophs for food and O2
earth’s supply of fossil fuels was formed from the remains of organisms that died hundreds of millions of years ago
fossil fuels are being consumed faster than they are being replenished
researchers are exploring methods of using the photosynthetic process to produce alternative fuels
chloroplasts - structurally similar to and likely evolved from photosynthetic bacteria
the structural organization of these organelles allows for the chemical reactions of photosynthesis
leaves are the major locations of photosynthesis in plants
chloroplasts are found mainly in cells of the mesophyll (the interior tissue of the leaf)
each mesophyll cell contains 30-40 chloroplasts
CO2 enters and O2 exits the leaf through microscopic pores called stomata
a chloroplast has an envelope of 2 membranes surrounding a dense fluid called the stroma
thylakoids are connected sacs in the chloroplast that compose a third membrane system
lamella connects the thylakoids
chlorophyll, the pigment that gives leaves their green color, resides in the thylakoid membranes
photosynthesis is a complex series of reactions that can be summarized as the equation:
6CO2 + 12H2O + light energy → C6H12O6 + 6O2 + 6H2O
the overall chemical change during photosynthesis is the reverse of the one that occurs during cellular respiration
chloroplasts split H2O into hydrogen and oxygen, incorporating the electrons of hydrogen into sugar molecules and releasing oxygen as a by-product
photosynthesis reverses the direction of electron flow compared to respiration
photosynthesis is a redox reaction in which H2O is oxidized and CO2 is reduced
photosynthesis is an endergonic process where the energy boost is provided by light
photosynthesis consists of light reactions (the photo part) and the Calvin cycle (the synthesis part)
the light reaction occurs in the thylakoids
splits H2O
releases O2
reduces the electron acceptor NADP+ to NADPH
(functionally the same as NAD and NADH)
generates ATP from ADP by photophosphorylation
the Calvin cycle occurs in the stroma and forms sugar from CO2 using ATP and NADPH
begins with carbon fixation, incorporating CO2 into organic molecules
chloroplasts are solar-powered chemical factories
their thylakoids transform light energy into the chemical energy of ATP and NADPH
light is electromagnetic energy, also called electromagnetic radiation
electromagnetic energy travels in rhythmic waves
wavelength is the distance between crests of electromagnetic waves
wavelength determines the type of electromagnetic energy
the electromagnetic spectrum is the entire range of electromagnetic energy or radiation
visible light consists of wavelengths (370nm to 750 nm) that produce colors we can see
visible light also includes the wavelengths that drive photosynthesis
plants tend to like light on the ends of the spectrum (red or violet)
photon energy is used from those two ends of the spectrum
light also behaves as though it consists of discrete particles called photons
the majority of plants are green bc it uses everything but the green waves/photons so they get reflected back to us
in autumn, leaves are reddish orange because those photons provide less energy and since there is already not enough energy from the sun at that it, it will prefer using waves on the shorter sides ( more energy)
pigments are substances that absorb visible light
different pigments absorb different wavelengths
wavelengths that are not absorbed are reflected or transmitted
leaves appear green because chlorophyll reflects and transmits green light
a spectrophotometer measures a pigment’s ability to absorb various wavelengths
this machine sends light through pigments and measures the fraction of light transmitted at each wavelength
an absorption spectrum is a graph plotting a pigment’s light absorption versus wavelength
there are 3 types of pigments in chloroplasts
chlorophyll a - the key light-capturing pigment
chlorophyll b - tan accessory pigment
carotenoids, a separate group of accessory pigments
do not produce as much sugar as chlorophyll
a and b differ by a functional group
the action spectrum profiles the relative effectiveness of different wavelengths of radiation in driving a process
the action spectrum of photosynthesis was first demonstrated in 1883 by Theodor W. Engelmann
in his experiment, he exposed different segments of filamentous alga to different wavelengths
areas receiving wavelengths favorable to photosynthesis produced excess O2
he used the growth of aerobic bacteria clustered along the alga as a measure of O2 production
the action spectrum for photosynthesis is broader than the absorption spectrum of chlorophyll
accessory pigments such as chlorophyll b broaden the spectrum for photosynthesis
the difference in the absorption spectrum between chlorophyll a and b is due to a slight structural difference between the pigment molecules
in chlorophyll a - methyl group
in chlorophyll b - carbonyl group
porphyrin ring - light absorbing head of molecule with magnesium at the center
hydrocarbon tail - interacts with hydrophobic regions of proteins inside the thylakoid membranes of chloroplasts
magnesium in the middle gives off electrons when light hits it which travel to the other parts of the molecule (replenishing electrons come from H2O)
accessory pigments called carotenoids may broaden the spectrum of colors that drive photosynthesis
some carotenoids function in photoprotection; they absorb excessive light that would damage chlorophyll or react with oxygen
a photosystem consists of a reaction-center complex surrounded by light-harvesting complexes
the reaction-center complex is an association of proteins holding a special pair of chlorophyll a molecules and primary electron acceptors
the light harvesting complex consists of pigment molecules bound to proteins
light-harvesting complexes transfer the energy of photons to the chlorophyll a molecules in the reaction-center complex
these chlorophyll a molecules are special because they can transfer an excited electron to a different molecule
a primary electron acceptor in the reaction center accepts excited electrons and is reduced as a result
solar-powered transfer of an electron from a chlorophyll a molecule to the primary electron acceptor is the first step of the light reactions
there are 2 types of photosystems in the thylakoid membrane
photosystem II (PSII) functions first
the reaction-center chlorophyll a of PS II is called P680 because it is best at absorbing a wavelength of 680 nm
photosystem I (PSI) - is best at absorbing a wavelength of 700nm
the reaction-center chlorophyll a of PSI is called P700
during the light reactions, there are 2 possible routes for electron flow
cyclic - electrons get recycled
linear - electrons leave the system
linear electron flow - the primary pathway involves both photosystems and produces ATP and NADPH using light energy
there are 8 steps to linear electron flow:
a photon hits a pigment in a light-harvesting complex of PSII and its energy is passed among pigment molecules until it excites P680
an excited electron from P680 is transferred to the primary electron acceptor and becomes P680+
H2O is split by enzymes and the electrons are transferred from the hydrogen atoms to P680+ reducing it to P680
P680+ is the strongest known biological oxidizing agent (oxidizes water)
the H+ are released into the thylakoid space
O2 is released as a by-product of this reaction
each electron “falls” down an electron transport chain from the primary electron acceptor of PSII to PSI. Energy released by the fall drives the creation of a proton gradient across the thylakoid membrane
potential energy stored in the proton gradient drives production of ATP by chemiosmosis
in PSI, transferred light energy excites P700 which loses an electron to the primary electron acceptor
P700+ accepts an electron passed down from PSII via the electron transport chain
each electron “falls” down an electron transport chain from the primary electron acceptor of PSI to the protein ferredoxin (Fd)
NADP+ reductase catalyzes the transfer of electrons to NADP+, reducing it to NADPH
the electrons of NADPH are available for the reactions of the Calvin cycle
the process also removes an H+ from the stroma
the energy changes of electrons during linear flow through the light reactions can be shown in a mechanical analogy
in cyclic electron flow, electrons cycle back from Fd to the PSI reaction center via a plastocyanin molecule (PC)
cyclic electron flow uses only photosystem I and produces ATP but not NADPH
no oxygen is released
some organisms such as purple sulphur bacteria and cyanobacteria have PSI but not PSII
cyclic electron flow is thought to have evolved before linear electron flow
cyclic electron flow may protect cells from light-induced damage
chloroplasts and mitochondria generate ATP by chemiosmosis but use different sources of energy
mitochondria transfer chemical energy from food to ATP; chloroplasts transform light energy into the chemical energy of ATP
spatial organization of chemiosmosis differs between chloroplasts and mitochondria but shows similarities
in mitochondria, protons are pumped to the intermembrane space and drive ATP synthesis as they diffuse back into the mitochondrial matrix
in chloroplasts, protons are pumped into the thylakoid space and drive ATP synthesis as they diffuse back into the stroma
ATP and NADPH are produced on the side facing the stroma where the calvin cycle takes place
in summary, light reactions generate ATP and increase the potential energy of electrons by moving them from H2O to NADPH
the calvin cycle, like the krebs cycle regenerates its starting material after molecules enter and leave the cycle
the calvin cycle is anabolic; it builds sugar from smaller molecules by using ATP and the reducing power of electrons carried by NADPH
carbons enter the cycle as CO2 and leave as G3P
for net synthesis of one G3P, the cycle must take place 3 times, fixing 3 molecules of CO2
the calvin cycle has 3 phases
carbon fixation (catalyzed by rubisco)
adding carbon onto a molecule
reduction
regeneration of the CO2 acceptor (RuBP)
rubisco is an enzyme that performs carbon fixation on RuBP
ATP, ADP and NADPH are produced
must go through the cycle 6 times for one glucose molecule to be made
6 CO2 used per glucose
dehydration is a problem for plants, sometimes requiring trade-offs with other metabolic processes, especially photosynthesis
on hot, dry days, plants close their stomata which conserves H2O but also limits photosynthesis
plants will make ATP and NADH during the day
at night, stomata will open and take CO2 to do the calvin cycle
cacti are acidic because they store CO2 as organic acid
the closing of stomata reduces access to CO2 and causes O2 to build up
having a lot of O2 causes an apparently wasteful process called photorespiration
in most plants (C3 plants), initial fixation of CO2 via rubisco forms a 3-carbon compound called 3-phosphoglycerate
because rubisco is such an old enzyme, it cannot tell the difference between O2 and CO2
in photorespiration, rubisco adds O2 instead of CO2 in the calvin cycle, producing a 2-carbon compound
photorespiration consumes O2 and organic fuel and releases CO2 without producing ATP or sugar
causes the whole cell to shut down
photorespiration may be an evolutionary relic because rubisco evolved at a time where O2 barely existed
photorespiration limits damaging products of light reactions that build up in the absence of the calvin cycle
in many plants, photorespiration is a problem because on a hot, dry day, it can drain as much as 50% of the carbon fixed by the calvin cycle
C4 plants minimize the cost of photorespiration by incorporating CO2 into 4-carbon compounds
there are 2 distant types of cells in the leaves of C4 plants
bundle sheath cells - arranged in tightly packed sheaths around the veins of the leaf
mesophyll cells - loosely packed between the bundle sheath and the leaf surface
sugar production in C4 plants occur in a 3 step process
the production of the 4-carbon precursors is catalyzed by the enzyme PEP carboxylase in the mesophyll cells
PEP carboxylase has a higher affinity for CO2 than rubisco does; it can fix CO2 even when concentrations are low
the 4-carbon compounds are exported to bundle sheath cells
within the bundle-sheath cells, they release CO2 that is then used in the calvin cycle
PEP carboxylase fixes CO2 with pyruvate (3C) to make malic acid (4C)
in the C4 pathway, the PEP carboxylase and the calvin cycle occur in different cells to prevent the rubisco from having access to O2 (stops photorespiration)
since the industrial revolution in the 1800s, CO2 levels have risen greatly
increasing levels of CO2 may affect C3 and C4 plants differently, perhaps changing the relative abundance of these species
the effects of such changes are unpredictable and a cause for concern
suitable agricultural land is decreasing due to the effects of climate change, while the world demand for food continues to increase
C4 photosynthesis uses less water and resources than C3 photosynthesis
scientists have genetically modified rice, a C3 plant, to carry out C4 photosynthesis
they estimate 30-50% increase in yield compared to C3 rice
some plants including succulents use crassulacean acid metabolism (CAM) to fix carbon
CAM plants open their stomata at night, incorporating CO2 into organic acids that are stored in the vacuoles
like pineapples
stomata close during the day and CO2 is released from organic acids and used in the Calvin cycle
the CAM pathway is similar to the C4 pathway in that they both incorporate CO2 into organic intermediates before it enters the calvin cycle
in the CAM pathway, these steps occur in the same cell but are separated by time
the energy entering chloroplasts as sunlight gets stored as chemical energy in organic compounds
sugar made in the chloroplasts supplies chemical energy and carbon skeletons to synthesize the organic molecules of cells
plants store excess sugar as starch in chloroplasts and other structures such as roots, tuber, seeds and fruits