Photosynthesis article provided by Encarta Encyclopedia 2000
PHOTOSYNTHESIS
INTRODUCTION
Photosynthesis, process by which green
plants and certain other organisms use the energy of
light to convert carbon dioxide and water into the
simple sugar glucose. In so doing, photosynthesis
provides the basic energy source for virtually all
organisms. An extremely important byproduct of
photosynthesis is oxygen, on which most organisms
depend.
Photosynthesis occurs in green plants, seaweeds,
algae, and certain bacteria. These organisms are
veritable sugar factories, producing millions of new
glucose molecules per second. Plants use much of this
glucose, a carbohydrate, as an energy source to build
leaves, flowers, fruits, and seeds. They also convert
glucose to cellulose, the structural material used in
their cell walls. Most plants produce more glucose
than they use, however, and they store it in the form
of starch and other carbohydrates in roots, stems, and
leaves. The plants can then draw on these reserves for
extra energy or building materials. Each year,
photosynthesizing organisms produce about 170 billion
metric tons of extra carbohydrates, about 30 metric
tons for every person on earth.
Photosynthesis has far-reaching implications. Like
plants, humans and other animals depend on glucose as
an energy source, but they are unable to produce it on
their own and must rely ultimately on the glucose
produced by plants. Moreover, the oxygen humans and
other animals breathe is the oxygen released during
photosynthesis. Humans are also dependent on ancient
products of photosynthesis, known as fossil fuels, for
supplying most of our modern industrial energy. These
fossil fuels, including natural gas, coal, and
petroleum, are composed of a complex mix of
hydrocarbons, the remains of organisms that relied on
photosynthesis millions of years ago. Thus, virtually
all life on earth, directly or indirectly, depends on
photosynthesis as a source of food, energy, and
oxygen, making it one of the most important
biochemical processes known.
WHERE PHOTOSYNTHESIS OCCURS
Plant photosynthesis occurs in leaves and green stems within specialized
cell structures called chloroplasts. One plant leaf is
composed of tens of thousands of cells, and each cell
contains 40 to 50 chloroplasts. The chloroplast, an
oval-shaped structure, is divided by membranes into
numerous disk-shaped compartments. These disklike
compartments, called thylakoids, are arranged
vertically in the chloroplast like a stack of plates
or pancakes. A stack of thylakoids is called a granum
(plural, grana); the grana lie suspended in a fluid
known as stroma.
Embedded in the membranes of the thylakoids are
hundreds of molecules of chlorophyll, a light-trapping
pigment required for photosynthesis. Additional
light-trapping pigments, enzymes (organic substances
that speed up chemical reactions), and other molecules
needed for photosynthesis are also located within the
thylakoid membranes. The pigments and enzymes are
arranged in two types of units, Photosystem I and
Photosystem II. Because a chloroplast may have dozens
of thylakoids, and each thylakoid may contain
thousands of photosystems, each chloroplast will
contain millions of pigment molecules.
HOW PHOTOSYNTHESIS WORKS
Photosynthesis is a very
complex process, and for the sake of convenience and
ease of understanding, plant biologists divide it into
two stages. In the first stage, the light-dependent
reaction, the chloroplast traps light energy and
converts it into chemical energy contained in
nicotinamide adenine dinucleotide phosphate (NADPH)
and adenosine triphosphate (ATP), two molecules used
in the second stage of photosynthesis. In the second
stage, called the light-independent reaction (formerly
called the dark reaction), NADPH provides the hydrogen
atoms that help form glucose, and ATP provides the
energy for this and other reactions used to synthesize
glucose. These two stages reflect the literal meaning
of the term photosynthesis, to build with light.
AThe Light-Dependent Reaction Photosynthesis relies on
flows of energy and electrons initiated by light
energy. Electrons are minute particles that travel in
a specific orbit around the nuclei of atoms and carry
a small electrical charge. Light energy causes the
electrons in chlorophyll and other light-trapping
pigments to boost up and out of their orbit; the
electrons instantly fall back into place, releasing
resonance energy, or vibrating energy, as they go, all
in millionths of a second.
Chlorophyll and the other pigments are clustered next to one another in the photosystems, and the vibrating energy passes rapidly
from one chlorophyll or pigment molecule to the next,
like the transfer of energy in billiard balls.
Light contains many colors, each with a defined range
of wavelengths measured in nanometers, or billionths
of a meter. Certain red and blue wavelengths of light
are the most effective in photosynthesis because they
have exactly the right amount of energy to energize,
or excite, chlorophyll electrons and boost them out of
their orbits to a higher energy level. Other pigments,
called accessory pigments, enhance the
light-absorption capacity of the leaf by capturing a
broader spectrum of blue and red wavelengths, along
with yellow and orange wavelengths. None of the
photosynthetic pigments absorb green light; as a
result, green wavelengths are reflected, which is why
plants appear green.
Photosynthesis begins when light strikes Photosystem I
pigments and excites their electrons. The energy
passes rapidly from molecule to molecule until it
reaches a special chlorophyll molecule called P700, so
named because it absorbs light in the red region of
the spectrum at wavelengths of 700 nanometers.
Until this point, only energy has moved from molecule
to molecule; now electrons themselves transfer between
molecules. P700 uses the energy of the excited
electrons to boost its own electrons to an energy
level that enables an adjoining electron acceptor
molecule to capture them. The electrons are then
passed down a chain of carrier molecules, called an
electron transport chain. The electrons are passed
from one carrier molecule to another in a downhill
direction, like individuals in a bucket brigade
passing water from the top of a hill to the bottom.
Each electron carrier is at a lower energy level than
the one before it, and the result is that electrons
release energy as they move down the chain. At the end
of the electron transport chain lies the molecule
nicotine adenine dinucleotide (NADP+). Using the
energy released by the flow of electrons, two
electrons from the electron transport chain combine
with a hydrogen ion and NADP+ to form NADPH.
When P700 transfers its electrons to the electron
acceptor, it becomes deficient in electrons. Before it
can function again, it must be replenished with new
electrons. Photosystem II accomplishes this task. As
in Photosystem I, light energy activates electrons of
the Photosystem II pigments. These pigments transfer
the energy of their excited electrons to a special
Photosystem II chlorophyll molecule, P680, that
absorbs light best in the red region at 680
nanometers. Just as in Photosystem I, energy is
transferred among pigment molecules and is then
directed to the P680 chlorophyll, where the energy is
used to transfer electrons from P680 to its adjoining
electron acceptor molecule.
From the Photosystem II electron acceptor, the
electrons are passed through a different electron
transport chain. As they pass along the cascade of
electron carrier molecules, the electrons give up some
of their energy to fuel the production of ATP, formed
by the addition of one phosphorous atom to adenosine
diphosphate (ADP). Eventually, the electron transport
carrier molecules deliver the Photosystem II electrons
to Photosystem I, which uses them to maintain the flow
of electrons to P700, thus restoring its function.
P680 in Photosystem II is now electron deficient
because it has donated electrons to P700 in
Photosystem I. P680 electrons are replenished by the
water that has been absorbed by the plant roots and
transported to the chloroplasts in the leaves. The
movement of electrons in Photosystems I and II and the
action of an enzyme split the water into oxygen,
hydrogen ions, and electrons. The electrons from water
flow to Photosystem II, replacing the electrons lost
by P680. Some of the hydrogen ions may be used to
produce NADPH at the end of the electron transport
chain, and the oxygen from the water diffuses out of
the chloroplast and is released into the atmosphere
through pores in the leaf.
The transfer of electrons in a step-by-step fashion in
Photosystems I and II releases energy and heat slowly,
thus protecting the chloroplast and cell from a
harmful temperature increase. It also provides time
for the plant to form NADPH and ATP. In the words of
American biochemist and Nobel laureate Albert
Szent-Gyorgyi, "What drives life is thus a little
electric current, set up by the sunshine."
BThe Light-Independent Reaction The chemical energy
required for the light-independent reaction is
supplied by the ATP and NADPH molecules produced in
the light-dependent reaction. The light-independent
reaction is cyclic, that is, it begins with a molecule
that must be regenerated at the end of the reaction in
order for the process to continue. Termed the Calvin
cycle after the American chemist Melvin Calvin who
discovered it, the light-independent reactions use the
electrons and hydrogen ions associated with NADPH and
the phosphorous associated with ATP to produce
glucose. These reactions occur in the stroma, the
fluid in the chloroplast surrounding the thylakoids,
and each step is controlled by a different enzyme.
The light-independent reaction requires the presence
of carbon dioxide molecules, which enter the plant
through pores in the leaf, diffuse through the cell to
the chloroplast, and disperse in the stroma. The
light-independent reaction begins in the stroma when
these carbon dioxide molecules link to sugar molecules
called ribulose bisphosphate (RuBP) in a process known
as carbon fixation.
With the help of an enzyme, six molecules of carbon
dioxide bond to six molecules of RuBP to create six
new molecules. Several intermediate steps, which
require ATP, NADPH, and additional enzymes, rearrange
the position of the carbon, hydrogen, and oxygen atoms
in these six molecules, and when the reactions are
complete, one new molecule of glucose has been
constructed and five molecules of RuBP have been
reconstructed. This process occurs repeatedly in each
chloroplast as long as carbon dioxide, ATP, and NADPH
are available. The thousands of glucose molecules
produced in this reaction are processed by the plant
to produce energy in the process known as aerobic
respiration, used as structural materials, or stored.
The regenerated RuBP is used to start the Calvin cycle
all over again.
PHOTOSYNTHESIS VARIATIONS
A majority of plants use these steps in photosynthesis. Plants such as corn and crabgrass that have evolved in hot, dry environments,
however, must overcome certain obstacles to
photosynthesis. On hot days, they partially close the
pores in their leaves to prevent the escape of water.
With the pores only slightly open, adequate amounts of
carbon dioxide cannot enter the leaf, and the Calvin
cycle comes to a halt. To get around this problem,
certain hot-weather plants have developed a way to
keep carbon dioxide flowing to the stroma without
capturing it directly from the air. They open their
pores slightly, take in carbon dioxide, and transport
it deep within the leaves. Here they stockpile it in a
chemical form that releases the carbon dioxide slowly
and steadily into the Calvin cycle. With this system,
these plants can continue photosynthesis on hot days,
even with their pores almost completely closed. A
field of corn thus remains green on blistering days
when neighboring plants wither, and crabgrass thrives
in lawns browned by the summer sun.
Bacteria lack chloroplasts, and instead use structures
called chromatophores-membranes formed by numerous
foldings of the plasma membrane, the membrane
surrounding the fluid, or cytoplasm, that fills the
cell. The chromatophores house thylakoids similar to
plant thylakoids, which in some bacteria contain
chlorophyll. For these bacteria, the process of
photosynthesis is similar to that of plants, algae,
and seaweed. Many of these chlorophyll-containing
bacteria are abundant in oceans, lakes, and rivers,
and the oxygen they release dissolves in the water and
enables fish and other aquatic organisms to survive.
Certain archaebacteria, members of a group of
primitive bacteria-like organisms, carry out
photosynthesis in a different manner. The mud-dwelling
green sulfur and purple sulfur archaebacteria use
hydrogen sulfide instead of water in photosynthesis.
These archaebacteria release sulfur rather than
oxygen, which, along with hydrogen sulfide, imparts
the rotten egg smell to mudflats. Halobacteria,
archaebacteria found in the salt flats of deserts,
rely on the pigment bacteriorhodopsin instead of
chlorophyll for photosynthesis. These archaebacteria
do not carry out the complete process of
photosynthesis; although they produce ATP in a process
similar to the light-dependent reaction and use it for
energy, they do not produce glucose. Halobacteria are
among the most ancient organisms, and may have been
the starting point for the evolution of
photosynthesis.
While it may seem that we understand photosynthesis in
detail, decades of experiments have given us only a
partial understanding of this important process. A
more thorough understanding of the details of
photosynthesis may pave the way for development of
crops that are more efficient at using the sun's
energy, producing food for increasingly bountiful
harvests.
"Photosynthesis," Microsoft® Encarta® Encyclopedia 2000. © 1993-1999 Microsoft Corporation. All rights reserved.