Chapter 10 Photosynthesis
Lecture Outline
Overview: The Process That
Feeds the Biosphere
·
Life
on Earth is solar powered.
·
The
chloroplasts of plants use a process called photosynthesis to capture light
energy from the sun and convert it to chemical energy stored in sugars and
other organic molecules.
Plants and other autotrophs are the producers
of the biosphere.
·
Photosynthesis
nourishes almost all the living world directly or indirectly.
°
All
organisms use organic compounds for energy and for carbon skeletons.
°
Organisms
obtain organic compounds by one of two major modes: autotrophic nutrition or
heterotrophic nutrition.
·
Autotrophs produce their organic
molecules from CO2 and other inorganic raw materials obtained from
the environment.
°
Autotrophs
are the ultimate sources of organic compounds for all heterotrophic organisms.
°
Autotrophs
are the producers of the biosphere.
·
Autotrophs
can be separated by the source of energy that drives their metabolism.
°
Photoautotrophs use light as a
source of energy to synthesize organic compounds.
§
Photosynthesis
occurs in plants, algae, some other protists, and some prokaryotes.
°
Chemoautotrophs harvest energy
from oxidizing inorganic substances, such as sulfur and ammonia.
§
Chemoautotrophy
is unique to prokaryotes.
·
Heterotrophs live on organic compounds
produced by other organisms.
°
These
organisms are the consumers of the
biosphere.
°
The
most obvious type of heterotrophs feeds on other organisms.
§
Animals
feed this way.
°
Other
heterotrophs decompose and feed on dead organisms or on organic litter, like
feces and fallen leaves.
§
Most
fungi and many prokaryotes get their nourishment this way.
°
Almost
all heterotrophs are completely dependent on photoautotrophs for food and for
oxygen, a by-product of photosynthesis.
Concept 10.1 Photosynthesis converts light energy
to the chemical energy of food
·
All
green parts of a plant have chloroplasts.
·
However,
the leaves are the major site of photosynthesis for most plants.
°
There
are about half a million chloroplasts per square millimeter of leaf surface.
·
The
color of a leaf comes from chlorophyll,
the green pigment in the chloroplasts.
°
Chlorophyll
plays an important role in the absorption of light energy during
photosynthesis.
·
Chloroplasts
are found mainly in mesophyll cells
forming the tissues in the interior of the leaf.
·
O2
exits and CO2 enters the leaf through microscopic pores called stomata in the leaf.
·
Veins
deliver water from the roots and carry off sugar from mesophyll cells to
nonphotosynthetic areas of the plant.
·
A
typical mesophyll cell has 30–40 chloroplasts, each about 2–4 microns by 4–7
microns long.
·
Each
chloroplast has two membranes around a central aqueous space, the stroma.
·
In
the stroma is an elaborate system of interconnected membranous sacs, the thylakoids.
°
The
interior of the thylakoids forms another compartment, the thylakoid space.
°
Thylakoids
may be stacked into columns called grana.
·
Chlorophyll
is located in the thylakoids.
°
Photosynthetic
prokaryotes lack chloroplasts.
°
Their
photosynthetic membranes arise from infolded regions of the plasma membranes,
folded in a manner similar to the thylakoid membranes of chloroplasts.
Evidence that chloroplasts split water
molecules enabled researchers to track atoms through photosynthesis.
·
Powered
by light, the green parts of plants produce organic compounds and O2
from CO2 and H2O.
·
The
equation describing the process of photosynthesis is:
°
6CO2 + 12H2O
+ light energy à C6H12O6
+ 6O2+ 6H2O
°
C6H12O6
is glucose.
·
Water
appears on both sides of the equation because 12 molecules of water are consumed,
and 6 molecules are newly formed during photosynthesis.
·
We
can simplify the equation by showing only the net consumption of water:
°
6CO2 + 6H2O
+ light energy à C6H12O6
+ 6O2
·
The
overall chemical change during photosynthesis is the reverse of cellular
respiration.
·
In
its simplest possible form: CO2 + H2O + light energy à [CH2O] + O2
°
[CH2O]
represents the general formula for a sugar.
·
One
of the first clues to the mechanism of photosynthesis came from the discovery
that the O2 given off by plants comes from H2O, not CO2.
°
Before
the 1930s, the prevailing hypothesis was that photosynthesis split carbon
dioxide and then added water to the carbon:
§
Step
1: CO2 à C + O2
§
Step
2: C + H2O à CH2O
°
C.
B. van Niel challenged this hypothesis.
°
In
the bacteria that he was studying, hydrogen sulfide (H2S), not
water, is used in photosynthesis.
°
These
bacteria produce yellow globules of sulfur as a waste, rather than oxygen.
°
Van
Niel proposed this chemical equation for photosynthesis in sulfur bacteria:
§
CO2
+ 2H2S à [CH2O] + H2O + 2S
·
He
generalized this idea and applied it to plants, proposing this reaction for
their photosynthesis:
°
CO2 + 2H2O
à [CH2O] + H2O +
O2
·
Thus,
van Niel hypothesized that plants split water as a source of electrons from
hydrogen atoms, releasing oxygen as a byproduct.
·
Other
scientists confirmed van Niel’s hypothesis twenty years later.
°
They
used 18O, a heavy isotope, as a tracer.
°
They
could label either C18O2 or H218O.
°
They
found that the 18O label only appeared in the oxygen produced in
photosynthesis when water was the source of the tracer.
·
Hydrogen
extracted from water is incorporated into sugar, and oxygen is released to the
atmosphere (where it can be used in respiration).
·
Photosynthesis
is a redox reaction.
°
It
reverses the direction of electron flow in respiration.
·
Water
is split and electrons transferred with H+ from water to CO2,
reducing it to sugar.
°
Because
the electrons increase in potential energy as they move from water to sugar,
the process requires energy.
°
The
energy boost is provided by light.
Here is a preview of the two stages of
photosynthesis.
·
Photosynthesis
is two processes, each with multiple stages.
·
The
light reactions (photo) convert solar energy to chemical energy.
·
The
Calvin cycle (synthesis) uses energy from the light reactions to incorporate CO2
from the atmosphere into sugar.
·
In
the light reactions, light energy absorbed by chlorophyll in the thylakoids
drives the transfer of electrons and hydrogen from water to NADP+ (nicotinamide adenine
dinucleotide phosphate), forming NADPH.
°
NADPH,
an electron acceptor, provides reducing power via energized electrons to the
Calvin cycle.
°
Water
is split in the process, and O2 is released as a by-product.
·
The
light reaction also generates ATP using chemiosmosis, in a process called photophosphorylation.
·
Thus
light energy is initially converted to chemical energy in the form of two
compounds: NADPH and ATP.
·
The
Calvin cycle is named for Melvin Calvin who, with his colleagues, worked out
many of its steps in the 1940s.
·
The
cycle begins with the incorporation of CO2 into organic molecules, a
process known as carbon fixation.
·
The
fixed carbon is reduced with electrons provided by NADPH.
·
ATP
from the light reactions also powers parts of the Calvin cycle.
·
Thus,
it is the Calvin cycle that makes sugar, but only with the help of ATP and
NADPH from the light reactions.
·
The
metabolic steps of the Calvin cycle are sometimes referred to as the
light-independent reactions, because none of the steps requires light directly.
·
Nevertheless,
the Calvin cycle in most plants occurs during daylight, because that is when
the light reactions can provide the NADPH and ATP the Calvin cycle requires.
·
While
the light reactions occur at the thylakoids, the Calvin cycle occurs in the
stroma.
Concept 10.2 The light reactions convert solar
energy to the chemical energy of ATP and NADPH
·
The
thylakoids convert light energy into the chemical energy of ATP and NADPH.
·
Light
is a form of electromagnetic radiation.
·
Like
other forms of electromagnetic energy, light travels in rhythmic waves.
·
The
distance between crests of electromagnetic waves is called the wavelength.
°
Wavelengths
of electromagnetic radiation range from less than a nanometer (gamma rays) to
more than a kilometer (radio waves).
·
The
entire range of electromagnetic radiation is the electromagnetic spectrum.
·
The
most important segment for life is a narrow band between 380 to 750 nm, the
band of visible light.
·
While
light travels as a wave, many of its properties are those of a discrete
particle, the photon.
°
Photons
are not tangible objects, but they do have fixed quantities of energy.
·
The
amount of energy packaged in a photon is inversely related to its wavelength.
°
Photons
with shorter wavelengths pack more energy.
·
While
the sun radiates a full electromagnetic spectrum, the atmosphere selectively
screens out most wavelengths, permitting only visible light to pass in
significant quantities.
°
Visible
light is the radiation that drives photosynthesis.
·
When
light meets matter, it may be reflected, transmitted, or absorbed.
°
Different
pigments absorb photons of different wavelengths, and the wavelengths that are
absorbed disappear.
°
A
leaf looks green because chlorophyll, the dominant pigment, absorbs red and
blue light, while transmitting and reflecting green light.
·
A
spectrophotometer measures the
ability of a pigment to absorb various wavelengths of light.
°
It
beams narrow wavelengths of light through a solution containing the pigment and
measures the fraction of light transmitted at each wavelength.
°
An
absorption spectrum plots a pigment’s
light absorption versus wavelength.
·
The
light reaction can perform work with those wavelengths of light that are
absorbed.
·
There
are several pigments in the thylakoid that differ in their absorption spectra.
°
Chlorophyll a, the dominant pigment, absorbs best in the
red and violet-blue wavelengths and least in the green.
°
Other
pigments with different structures have different absorption spectra.
·
Collectively,
these photosynthetic pigments determine an overall action spectrum for photosynthesis.
°
An
action spectrum measures changes in some measure of photosynthetic activity
(for example, O2 release) as the wavelength is varied.
·
The
action spectrum of photosynthesis was first demonstrated in 1883 in an elegant
experiment performed by Thomas Engelmann.
°
In
this experiment, different segments of a filamentous alga were exposed to
different wavelengths of light.
°
Areas
receiving wavelengths favorable to photosynthesis produced excess O2.
°
Engelmann
used the abundance of aerobic bacteria that clustered along the alga at
different segments as a measure of O2 production.
·
The
action spectrum of photosynthesis does not match exactly the absorption
spectrum of any one photosynthetic pigment, including chlorophyll a.
·
Only
chlorophyll a participates directly
in the light reaction, but accessory photosynthetic pigments absorb light and
transfer energy to chlorophyll a.
°
Chlorophyll b, with a slightly different structure than
chlorophyll a, has a slightly
different absorption spectrum and funnels the energy from these wavelengths to
chlorophyll a.
°
Carotenoids can funnel the energy
from other wavelengths to chlorophyll a
and also participate in photoprotection
against excessive light.
°
These
compounds absorb and dissipate excessive light energy that would otherwise
damage chlorophyll.
°
They
also interact with oxygen to form reactive oxidative molecules that could
damage the cell.
·
When
a molecule absorbs a photon, one of that molecule’s electrons is elevated to an
orbital with more potential energy.
°
The
electron moves from its ground state to an excited state.
°
The
only photons that a molecule can absorb are those whose energy matches exactly
the energy difference between the ground state and excited state of this
electron.
°
Because
this energy difference varies among atoms and molecules, a particular compound
absorbs only photons corresponding to specific wavelengths.
°
Thus,
each pigment has a unique absorption spectrum.
·
Excited
electrons are unstable.
·
Generally,
they drop to their ground state in a billionth of a second, releasing heat
energy.
·
Some
pigments, including chlorophyll, can also release a photon of light in a
process called fluorescence.
°
If
a solution of chlorophyll isolated from chloroplasts is illuminated, it will
fluoresce and give off heat.
·
Chlorophyll
excited by absorption of light energy produces very different results in an
intact chloroplast than it does in isolation.
·
In
the thylakoid membrane, chlorophyll is organized along with proteins and
smaller organic molecules into photosystems.
·
A
photosystem is composed of a reaction center surrounded by a light-harvesting
complex.
·
Each
light-harvesting complex consists of
pigment molecules (which may include chlorophyll a, chlorophyll b, and
carotenoid molecules) bound to particular proteins.
·
Together,
these light-harvesting complexes act like light-gathering “antenna complexes”
for the reaction center.
·
When
any antenna molecule absorbs a photon, it is transmitted from molecule to
molecule until it reaches a particular chlorophyll a molecule, the reaction
center.
·
At
the reaction center is a primary
electron acceptor, which accepts an excited electron from the reaction
center chlorophyll a.
°
The
solar-powered transfer of an electron from a special chlorophyll a molecule to the primary electron
acceptor is the first step of the light reactions.
·
Each
photosystem—reaction-center chlorophyll and primary electron acceptor
surrounded by an antenna complex—functions in the chloroplast as a
light-harvesting unit.
·
There
are two types of photosystems in the thylakoid membrane.
°
Photosystem I (PS I) has a reaction center
chlorophyll a that has an absorption
peak at 700 nm.
°
Photosystem II (PS II) has a reaction center
chlorophyll a that has an absorption
peak at 680 nm.
°
The
differences between these reaction centers (and their absorption spectra) lie
not in the chlorophyll molecules, but in the proteins associated with each
reaction center.
°
These
two photosystems work together to use light energy to generate ATP and NADPH.
·
During
the light reactions, there are two possible routes for electron flow: cyclic
and noncyclic.
·
Noncyclic electron flow, the predominant route,
produces both ATP and NADPH.
1. Photosystem II absorbs a
photon of light. One of the electrons of P680 is excited to a higher energy
state.
2. This electron is captured
by the primary electron acceptor, leaving the reaction center oxidized.
3. An enzyme extracts
electrons from water and supplies them to the oxidized reaction center. This
reaction splits water into two hydrogen ions and an oxygen atom that combines
with another oxygen atom to form O2.
4. Photoexcited electrons
pass along an electron transport chain before ending up at an oxidized
photosystem I reaction center.
5. As these electrons “fall”
to a lower energy level, their energy is harnessed to produce ATP.
6. Meanwhile, light energy
has excited an electron of PS I’s P700 reaction center. The photoexcited
electron was captured by PS I’s primary electron acceptor, creating an electron
“hole” in P700. This hole is filled by an electron that reaches the bottom of
the electron transport chain from PS II.
7. Photoexcited electrons are
passed from PS I’s primary electron acceptor down a second electron transport
chain through the protein ferredoxin (Fd).
8. The enzyme NADP+
reductase transfers electrons from Fd to NADP+. Two electrons are
required for NADP+’s reduction to NADPH. NADPH will carry the
reducing power of these high-energy electrons to the Calvin cycle.
·
The
light reactions use the solar power of photons absorbed by both photosystem I
and photosystem II to provide chemical energy in the form of ATP and reducing
power in the form of the electrons carried by NADPH.
·
Under
certain conditions, photoexcited electrons from photosystem I, but not
photosystem II, can take an alternative pathway, cyclic electron flow.
°
Excited
electrons cycle from their reaction center to a primary acceptor, along an
electron transport chain, and return to the oxidized P700 chlorophyll.
°
As
electrons flow along the electron transport chain, they generate ATP by cyclic photophosphorylation.
°
There
is no production of NADPH and no release of oxygen.
·
What
is the function of cyclic electron flow?
·
Noncyclic
electron flow produces ATP and NADPH in roughly equal quantities.
·
However,
the Calvin cycle consumes more ATP than NADPH.
·
Cyclic
electron flow allows the chloroplast to generate enough surplus ATP to satisfy
the higher demand for ATP in the Calvin cycle.
·
Chloroplasts
and mitochondria generate ATP by the same mechanism: chemiosmosis.
°
In
both organelles, an electron transport chain pumps protons across a membrane as
electrons are passed along a series of increasingly electronegative carriers.
°
This
transforms redox energy to a proton-motive force in the form of an H+
gradient across the membrane.
°
ATP
synthase molecules harness the proton-motive force to generate ATP as H+
diffuses back across the membrane.
·
Some
of the electron carriers, including the cytochromes, are very similar in
chloroplasts and mitochondria.
·
The
ATP synthase complexes of the two organelles are also very similar.
·
There
are differences between oxidative phosphorylation in mitochondria and
photophosphorylation in chloroplasts.
·
Mitochondria
transfer chemical energy from food molecules to ATP; chloroplasts transform
light energy into the chemical energy of ATP.
·
The
spatial organization of chemiosmosis also differs in the two organelles.
·
The
inner membrane of the mitochondrion pumps protons from the mitochondrial matrix
out to the intermembrane space. The thylakoid membrane of the chloroplast pumps
protons from the stroma into the thylakoid space inside the thylakoid.
·
The
thylakoid membrane makes ATP as the hydrogen ions diffuse down their
concentration gradient from the thylakoid space back to the stroma through ATP
synthase complexes, whose catalytic knobs are on the stroma side of the
membrane.
·
The
proton gradient, or pH gradient, across the thylakoid membrane is substantial.
°
When
chloroplasts are illuminated, the pH in the thylakoid space drops to about 5
and the pH in the stroma increases to about 8, a thousandfold different in H+
concentration.
·
The
light-reaction “machinery” produces ATP and NADPH on the stroma side of the
thylakoid.
·
Noncyclic
electron flow pushes electrons from water, where they have low potential
energy, to NADPH, where they have high potential energy.
°
This
process also produces ATP and oxygen as a by-product.
Concept 10.3 The Calvin cycle uses ATP and NADPH
to convert CO2 to sugar
·
The
Calvin cycle regenerates its starting material after molecules enter and leave
the cycle.
·
The
Calvin cycle is anabolic, using energy to build sugar from smaller molecules.
·
Carbon
enters the cycle as CO2 and leaves as sugar.
·
The
cycle spends the energy of ATP and the reducing power of electrons carried by
NADPH to make sugar.
·
The
actual sugar product of the Calvin cycle is not glucose, but a three-carbon
sugar, glyceraldehyde-3-phosphate (G3P).
·
Each
turn of the Calvin cycle fixes one carbon.
·
For
the net synthesis of one G3P molecule, the cycle must take place three times,
fixing three molecules of CO2.
·
To
make one glucose molecule requires six cycles and the fixation of six CO2
molecules.
·
The
Calvin cycle has three phases.
Phase 1: Carbon fixation
·
In
the carbon fixation phase, each CO2
molecule is attached to a five-carbon sugar, ribulose bisphosphate (RuBP).
°
This
is catalyzed by RuBP carboxylase or rubisco.
°
Rubisco
is the most abundant protein in chloroplasts and probably the most abundant
protein on Earth.
°
The
six-carbon intermediate is unstable and splits in half to form two molecules of
3-phosphoglycerate for each CO2.
Phase 2: Reduction
·
During
reduction, each 3-phosphoglycerate
receives another phosphate group from ATP to form 1,3-bisphosphoglycerate.
·
A
pair of electrons from NADPH reduces each 1,3-bisphosphoglycerate to G3P.
°
The
electrons reduce a carboxyl group to the aldehyde group of G3P, which stores
more potential energy.
·
If
our goal was the net production of one G3P, we would start with 3CO2
(3C) and three RuBP (15C).
·
After
fixation and reduction, we would have six molecules of G3P (18C).
°
One
of these six G3P (3C) is a net gain of carbohydrate.
§
This
molecule can exit the cycle and be used by the plant cell.
Phase 3: Regeneration
·
The
other five G3P (15C) remain in the cycle to regenerate three RuBP. In a complex series of reactions, the carbon
skeletons of five molecules of G3P are rearranged by the last steps of the
Calvin cycle to regenerate three molecules of RuBP.
·
For
the net synthesis of one G3P molecule, the Calvin cycle consumes nine ATP and
six NADPH.
·
The
light reactions regenerate ATP and NADPH.
·
The
G3P from the Calvin cycle is the starting material for metabolic pathways that
synthesize other organic compounds, including glucose and other carbohydrates.
Concept 10.4 Alternative mechanisms of carbon
fixation have evolved in hot, arid climates
·
One
of the major problems facing terrestrial plants is dehydration.
·
At
times, solutions to this problem require tradeoffs with other metabolic
processes, especially photosynthesis.
·
The
stomata are not only the major route for gas exchange (CO2 in and O2
out), but also for the evaporative loss of water.
·
On
hot, dry days, plants close their stomata to conserve water. This causes
problems for photosynthesis.
·
In
most plants (C3 plants),
initial fixation of CO2 occurs via rubisco, forming a three-carbon
compound, 3-phosphoglycerate.
°
C3
plants include rice, wheat, and soybeans.
·
When
their stomata partially close on a hot, dry day, CO2 levels drop as
CO2 is consumed in the Calvin cycle.
·
At
the same time, O2 levels rise as the light reaction converts light
to chemical energy.
·
While
rubisco normally accepts CO2, when the O2:CO2
ratio increases (on a hot, dry day with closed stomata), rubisco can add O2
to RuBP.
·
When
rubisco adds O2 to RuBP, RuBP splits into a three-carbon piece and a
two-carbon piece in a process called photorespiration.
°
The
two-carbon fragment is exported from the chloroplast and degraded to CO2
by mitochondria and peroxisomes.
°
Unlike
normal respiration, this process produces no ATP.
§
In
fact, photorespiration consumes ATP.
°
Unlike
photosynthesis, photorespiration does not produce organic molecules.
§
In
fact, photorespiration decreases
photosynthetic output by siphoning organic material from the Calvin cycle.
·
A
hypothesis for the existence of photorespiration is that it is evolutionary
baggage.
·
When
rubisco first evolved, the atmosphere had far less O2 and more CO2
than it does today.
°
The
inability of the active site of rubisco to exclude O2 would have
made little difference.
·
Today
it does make a difference.
°
Photorespiration
can drain away as much as 50% of the carbon fixed by the Calvin cycle on a hot,
dry day.
·
Certain
plant species have evolved alternate modes of carbon fixation to minimize
photorespiration.
·
C4 plants first fix CO2
in a four-carbon compound.
°
Several
thousand plants, including sugarcane and corn, use this pathway.
·
A
unique leaf anatomy is correlated with the mechanism of C4
photosynthesis.
·
In
C4 plants, there are two distinct types of photosynthetic cells:
bundle-sheath cells and mesophyll cells.
°
Bundle-sheath cells are arranged into tightly
packed sheaths around the veins of the leaf.
°
Mesophyll cells are more loosely arranged
cells located between the bundle sheath and the leaf surface.
·
The
Calvin cycle is confined to the chloroplasts of the bundle-sheath cells.
·
However,
the cycle is preceded by the incorporation of CO2 into organic
molecules in the mesophyll.
·
The
key enzyme, phosphoenolpyruvate carboxylase, adds CO2 to
phosphoenolpyruvate (PEP) to form oxaloacetate.
°
PEP carboxylase has a very high affinity
for CO2 and can fix CO2 efficiently when rubisco cannot
(i.e., on hot, dry days when the stomata are closed).
·
The
mesophyll cells pump these four-carbon compounds into bundle-sheath cells.
°
The
bundle-sheath cells strip a carbon from the four-carbon compound as CO2,
and return the three-carbon remainder to the mesophyll cells.
°
The
bundle-sheath cells then use rubisco to start the Calvin cycle with an abundant
supply of CO2.
·
In
effect, the mesophyll cells pump CO2 into the bundle-sheath cells,
keeping CO2 levels high enough for rubisco to accept CO2
and not O2.
·
C4
photosynthesis minimizes photorespiration and enhances sugar production.
·
C4
plants thrive in hot regions with intense sunlight.
·
A
second strategy to minimize photorespiration is found in succulent plants,
cacti, pineapples, and several other plant families.
°
These
plants are known as
°
They
open their stomata during the night and close them during the day.
§
Temperatures
are typically lower at night, and humidity is higher.
°
During
the night, these plants fix CO2 into a variety of organic acids in
mesophyll cells.
°
During
the day, the light reactions supply ATP and NADPH to the Calvin cycle, and CO2
is released from the organic acids.
·
Both
C4 and
°
In
C4 plants, carbon fixation and the Calvin cycle are spatially
separated.
°
In
·
Both
eventually use the Calvin cycle to make sugar from carbon dioxide.
Here is a review of the importance of
photosynthesis.
·
In
photosynthesis, the energy that enters the chloroplasts as sunlight becomes
stored as chemical energy in organic compounds.
·
Sugar
made in the chloroplasts supplies the entire plant with chemical energy and
carbon skeletons to synthesize all the major organic molecules of cells.
°
About
50% of the organic material is consumed as fuel for cellular respiration in
plant mitochondria.
°
Carbohydrate
in the form of the disaccharide sucrose travels via the veins to
nonphotosynthetic cells.
§
There,
it provides fuel for respiration and the raw materials for anabolic pathways,
including synthesis of proteins and lipids and formation of the extracellular
polysaccharide cellulose.
§
Cellulose,
the main ingredient of cell walls, is the most abundant organic molecule in the
plant, and probably on the surface of the planet.
·
Plants
also store excess sugar by synthesis of starch.
°
Starch
is stored in chloroplasts and in storage cells in roots, tubers, seeds, and
fruits.
·
Heterotrophs,
including humans, may completely or partially consume plants for fuel and raw
materials.
·
On
a global scale, photosynthesis is the most important process on Earth.
°
It
is responsible for the presence of oxygen in our atmosphere.
°
Each
year, photosynthesis synthesizes 160 billion metric tons of carbohydrate.