Photosynthesis

42 The Light-Dependent Reactions of Photosynthesis

Learning Objectives

By the end of this section, you will be able to do the following:

  • Explain how plants absorb energy from sunlight
  • Describe short and long wavelengths of light
  • Describe how and where photosynthesis takes place within a plant

How can light energy be used to make food? When a person turns on a lamp, electrical energy becomes light energy. Like all other forms of kinetic energy, light can travel, change form, and be harnessed to do work. In the case of photosynthesis, light energy is converted into chemical energy, which photoautotrophs use to build basic carbohydrate molecules ((Figure)). However, autotrophs only use a few specific wavelengths of sunlight.

Photoautotrophs can capture visible light energy in specific wavelengths from the sun, converting it into the chemical energy used to build food molecules. (credit: Gerry Atwell)


A photo shows the silhouette of a grassy plant against the sun at sunset.

What Is Light Energy?

The sun emits an enormous amount of electromagnetic radiation (solar energy in a spectrum from very short gamma rays to very long radio waves). Humans can see only a tiny fraction of this energy, which we refer to as “visible light.” The manner in which solar energy travels is described as waves. Scientists can determine the amount of energy of a wave by measuring its wavelength (shorter wavelengths are more powerful than longer wavelengths)—the distance between consecutive crest points of a wave. Therefore, a single wave is measured from two consecutive points, such as from crest to crest or from trough to trough ((Figure)).

The wavelength of a single wave is the distance between two consecutive points of similar position (two crests or two troughs) along the wave.


The illustration shows two waves. The distance between the crests (or troughs) is the wavelength.  The crest is the upper portion of the wave, the trough is the lower portion of the wave.

Visible light constitutes only one of many types of electromagnetic radiation emitted from the sun and other stars. Scientists differentiate the various types of radiant energy from the sun within the electromagnetic spectrum. The electromagnetic spectrum is the range of all possible frequencies of radiation ((Figure)). The difference between wavelengths relates to the amount of energy carried by them.

The sun emits energy in the form of electromagnetic radiation. This radiation exists at different wavelengths, each of which has its own characteristic energy. All electromagnetic radiation, including visible light, is characterized by its wavelength.


The illustration lists the types of electromagnetic radiation in order of increasing wavelength. These include gamma rays, X-rays, ultraviolet, visible, infrared, and radio. Gamma rays have a very short wavelength, on the order of one thousandth of a nanometer. Radio waves have a very long wavelength, on the order of one kilometer. Visible light ranges from 380 nanometers at the violet end of the spectrum, to 750 nanometers at the red end of the spectrum.

Each type of electromagnetic radiation travels at a particular wavelength. The longer the wavelength, the less energy it carries. Short, tight waves carry the most energy. This may seem illogical, but think of it in terms of a piece of moving heavy rope. It takes little effort by a person to move a rope in long, wide waves. To make a rope move in short, tight waves, a person would need to apply significantly more energy.

The electromagnetic spectrum ((Figure)) shows several types of electromagnetic radiation originating from the sun, including X-rays and ultraviolet (UV) rays. The higher-energy waves can penetrate tissues and damage cells and DNA, which explains why both X-rays and UV rays can be harmful to living organisms.

Absorption of Light

Light energy initiates the process of photosynthesis when pigments absorb specific wavelengths of visible light. Organic pigments, whether in the human retina or the chloroplast thylakoid, have a narrow range of energy levels that they can absorb. Energy levels lower than those represented by red light are insufficient to raise an orbital electron to a excited (quantum) state. Energy levels higher than those in blue light will physically tear the molecules apart, in a process called bleaching. Our retinal pigments can only “see” (absorb) wavelengths between 700 nm and 400 nm of light, a spectrum that is therefore called visible light. For the same reasons, plants, pigment molecules absorb only light in the wavelength range of 700 nm to 400 nm; plant physiologists refer to this range for plants as photosynthetically active radiation.

The visible light seen by humans as white light actually exists in a rainbow of colors. Certain objects, such as a prism or a drop of water, disperse white light to reveal the colors to the human eye. The visible light portion of the electromagnetic spectrum shows the rainbow of colors, with violet and blue having shorter wavelengths, and therefore higher energy. At the other end of the spectrum toward red, the wavelengths are longer and have lower energy ((Figure)).

The colors of visible light do not carry the same amount of energy. Violet has the shortest wavelength and therefore carries the most energy, whereas red has the longest wavelength and carries the least amount of energy. (credit: modification of work by NASA)


The illustration shows the colors of visible light. In order of decreasing wavelength, these are red, orange, yellow, green, blue, indigo, and violet.

Understanding Pigments

Different kinds of pigments exist, and each absorbs only specific wavelengths (colors) of visible light. Pigments reflect or transmit the wavelengths they cannot absorb, making them appear a mixture of the reflected or transmitted light colors.

Chlorophylls and carotenoids are the two major classes of photosynthetic pigments found in plants and algae; each class has multiple types of pigment molecules. There are five major chlorophylls: a, b, c and d and a related molecule found in prokaryotes called bacteriochlorophyll. Chlorophyll a and chlorophyll b are found in higher plant chloroplasts and will be the focus of the following discussion.

With dozens of different forms, carotenoids are a much larger group of pigments. The carotenoids found in fruit—such as the red of tomato (lycopene), the yellow of corn seeds (zeaxanthin), or the orange of an orange peel (β-carotene)—are used as advertisements to attract seed dispersers. In photosynthesis, carotenoids function as photosynthetic pigments that are very efficient molecules for the disposal of excess energy. When a leaf is exposed to full sun, the light-dependent reactions are required to process an enormous amount of energy; if that energy is not handled properly, it can do significant damage. Therefore, many carotenoids reside in the thylakoid membrane, absorb excess energy, and safely dissipate that energy as heat.

Each type of pigment can be identified by the specific pattern of wavelengths it absorbs from visible light: This is termed the absorption spectrum. The graph in (Figure) shows the absorption spectra for chlorophyll a, chlorophyll b, and a type of carotenoid pigment called β-carotene (which absorbs blue and green light). Notice how each pigment has a distinct set of peaks and troughs, revealing a highly specific pattern of absorption. Chlorophyll a absorbs wavelengths from either end of the visible spectrum (blue and red), but not green. Because green is reflected or transmitted, chlorophyll appears green. Carotenoids absorb in the short-wavelength blue region, and reflect the longer yellow, red, and orange wavelengths.

(a) Chlorophyll a, (b) chlorophyll b, and (c) β-carotene are hydrophobic organic pigments found in the thylakoid membrane. Chlorophyll a and b, which are identical except for the part indicated in the red box, are responsible for the green color of leaves. β-carotene is responsible for the orange color in carrots. Each pigment has (d) a unique absorbance spectrum.


Chlorophyll a and chlorophyll b are made up of a long hydrocarbon chain attached to a large, complex ring made up of nitrogen and carbon. Magnesium is associated with the center of the ring. Chlorophyll b differs from chlorophyll a in that it has a C H O group instead of a C H 3 group associated with one part of the ring. Beta-carotene is a branched hydrocarbon with a six-membered carbon ring at each end. Each chart shows the absorbance spectra for chlorophyll a, chlorophyll b, and beta-carotene. The three pigments absorb blue-green and orange-red wavelengths of light but have slightly different spectra.

Many photosynthetic organisms have a mixture of pigments, and by using these pigments, the organism can absorb energy from a wider range of wavelengths. Not all photosynthetic organisms have full access to sunlight. Some organisms grow underwater where light intensity and quality decrease and change with depth. Other organisms grow in competition for light. Plants on the rainforest floor must be able to absorb any bit of light that comes through, because the taller trees absorb most of the sunlight and scatter the remaining solar radiation ((Figure)).

Plants that commonly grow in the shade have adapted to low levels of light by changing the relative concentrations of their chlorophyll pigments. (credit: Jason Hollinger)


The photo shows undergrowth in a forest.

When studying a photosynthetic organism, scientists can determine the types of pigments present by generating absorption spectra. An instrument called a spectrophotometer can differentiate which wavelengths of light a substance can absorb. Spectrophotometers measure transmitted light and compute from it the absorption. By extracting pigments from leaves and placing these samples into a spectrophotometer, scientists can identify which wavelengths of light an organism can absorb. Additional methods for the identification of plant pigments include various types of chromatography that separate the pigments by their relative affinities to solid and mobile phases.

How Light-Dependent Reactions Work

The overall function of light-dependent reactions is to convert solar energy into chemical energy in the form of NADPH and ATP. This chemical energy supports the light-independent reactions and fuels the assembly of sugar molecules. The light-dependent reactions are depicted in (Figure). Protein complexes and pigment molecules work together to produce NADPH and ATP. The numbering of the photosystems is derived from the order in which they were discovered, not in the order of the transfer of electrons.

A photosystem consists of 1) a light-harvesting complex and 2) a reaction center. Pigments in the light-harvesting complex pass light energy to two special chlorophyll a molecules in the reaction center. The light excites an electron from the chlorophyll a pair, which passes to the primary electron acceptor. The excited electron must then be replaced. In (a) photosystem II, the electron comes from the splitting of water, which releases oxygen as a waste product. In (b) photosystem I, the electron comes from the chloroplast electron transport chain discussed below.


Illustration a shows the structure of P S I I, which is embedded in the thylakoid membrane. At the core of P S I I is the reaction center. The reaction center is surrounded by the light-harvesting complex, which contains antenna pigment molecules that shunt light energy toward a pair of chlorophyll a molecules in the reaction center. As a result, an electron is excited and transferred to the primary electron acceptor. A water molecule is split, releasing two electrons which are used to replace excited electrons. Illustration b shows the structure of P S I, which is similar in structure to P S I I. However, P S I I uses an electron from the chloroplast electron transport chain also embedded in the thylakoid membrane to replace the excited electron.

The actual step that converts light energy into chemical energy takes place in a multiprotein complex called a photosystem, two types of which are found embedded in the thylakoid membrane: photosystem II (PSII) and photosystem I (PSI) ((Figure)). The two complexes differ on the basis of what they oxidize (that is, the source of the low-energy electron supply) and what they reduce (the place to which they deliver their energized electrons).

Both photosystems have the same basic structure; a number of antenna proteins to which the chlorophyll molecules are bound surround the reaction center where the photochemistry takes place. Each photosystem is serviced by the light-harvesting complex, which passes energy from sunlight to the reaction center; it consists of multiple antenna proteins that contain a mixture of 300 to 400 chlorophyll a and b molecules as well as other pigments like carotenoids. The absorption of a single photon or distinct quantity or “packet” of light by any of the chlorophylls pushes that molecule into an excited state. In short, the light energy has now been captured by biological molecules but is not stored in any useful form yet. The energy is transferred from chlorophyll to chlorophyll until eventually (after about a millionth of a second), it is delivered to the reaction center. Up to this point, only energy has been transferred between molecules, not electrons.

Visual Connection
In the photosystem II (PSII) reaction center, energy from sunlight is used to extract electrons from water. The electrons travel through the chloroplast electron transport chain to photosystem I (PSI), which reduces NADP+ to NADPH. The electron transport chain moves protons across the thylakoid membrane into the lumen. At the same time, splitting of water adds protons to the lumen, and reduction of NADPH removes protons from the stroma. The net result is a low pH in the thylakoid lumen, and a high pH in the stroma. ATP synthase uses this electrochemical gradient to make ATP.


This illustration shows the components involved in the light reactions, which are all embedded in the thylakoid membrane. Photosystem I I uses light energy to strip electrons from water, producing half an oxygen molecule and two protons in the process. The excited electron is then passed through the chloroplast electron transport chain to photosystem I. Photosystem I passes the electron to N A D P superscript plus sign baseline reductase, which uses it to convert N A D P superscript plus sign baseline and a proton to N A D P H. As the electron transport chain moves electrons, it pumps protons into the thylakoid lumen. The splitting of water also adds electrons to the lumen, and the reduction of N A D P H removes protons from the stroma. The net result is a low lower case p upper case H inside the thylakoid lumen, and a high lower p upper H outside, in the stroma. A T P synthase embedded the thylakoid  membrane moves protons down their electrochemical gradient, from the lumen to the stroma, and uses the energy from this gradient to make A T P.

What is the initial source of electrons for the chloroplast electron transport chain?

  1. water
  2. oxygen
  3. carbon dioxide
  4. NADPH

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The reaction center contains a pair of chlorophyll a molecules with a special property. Those two chlorophylls can undergo oxidation upon excitation; they can actually give up an electron in a process called a photoact. It is at this step in the reaction center during photosynthesis that light energy is converted into an excited electron. All of the subsequent steps involve getting that electron onto the energy carrier NADPH for delivery to the Calvin cycle where the electron is deposited onto carbon for long-term storage in the form of a carbohydrate. PSII and PSI are two major components of the photosynthetic electron transport chain, which also includes the cytochrome complex. The cytochrome complex, an enzyme composed of two protein complexes, transfers the electrons from the carrier molecule plastoquinone (Pq) to the protein plastocyanin (Pc), thus enabling both the transfer of protons across the thylakoid membrane and the transfer of electrons from PSII to PSI.

The reaction center of PSII (called P680) delivers its high-energy electrons, one at the time, to the primary electron acceptor, and through the electron transport chain (Pq to cytochrome complex to plastocyanine) to PSI. P680’s missing electron is replaced by extracting a low-energy electron from water; thus, water is “split” during this stage of photosynthesis, and PSII is re-reduced after every photoact. Splitting one H2O molecule releases two electrons, two hydrogen atoms, and one atom of oxygen. However, splitting two molecules is required to form one molecule of diatomic O2 gas. About 10 percent of the oxygen is used by mitochondria in the leaf to support oxidative phosphorylation. The remainder escapes to the atmosphere where it is used by aerobic organisms to support respiration.

As electrons move through the proteins that reside between PSII and PSI, they lose energy. This energy is used to move hydrogen atoms from the stromal side of the membrane to the thylakoid lumen. Those hydrogen atoms, plus the ones produced by splitting water, accumulate in the thylakoid lumen and will be used synthesize ATP in a later step. Because the electrons have lost energy prior to their arrival at PSI, they must be re-energized by PSI, hence, another photon is absorbed by the PSI antenna. That energy is relayed to the PSI reaction center (called P700). P700 is oxidized and sends a high-energy electron to NADP+ to form NADPH. Thus, PSII captures the energy to create proton gradients to make ATP, and PSI captures the energy to reduce NADP+ into NADPH. The two photosystems work in concert, in part, to guarantee that the production of NADPH will roughly equal the production of ATP. Other mechanisms exist to fine-tune that ratio to exactly match the chloroplast’s constantly changing energy needs.

Generating an Energy Carrier: ATP

As in the intermembrane space of the mitochondria during cellular respiration, the buildup of hydrogen ions inside the thylakoid lumen creates a concentration gradient. The passive diffusion of hydrogen ions from high concentration (in the thylakoid lumen) to low concentration (in the stroma) is harnessed to create ATP, just as in the electron transport chain of cellular respiration. The ions build up energy because of diffusion and because they all have the same electrical charge, repelling each other.

To release this energy, hydrogen ions will rush through any opening, similar to water jetting through a hole in a dam. In the thylakoid, that opening is a passage through a specialized protein channel called the ATP synthase. The energy released by the hydrogen ion stream allows ATP synthase to attach a third phosphate group to ADP, which forms a molecule of ATP ((Figure)). The flow of hydrogen ions through ATP synthase is called chemiosmosis because the ions move from an area of high to an area of low concentration through a semi-permeable structure of the thylakoid.

Link to Learning

Visit this site and click through the animation to view the process of photosynthesis within a leaf.

Section Summary

The pigments of the first part of photosynthesis, the light-dependent reactions, absorb energy from sunlight. A photon strikes the antenna pigments of photosystem II to initiate photosynthesis. The energy travels to the reaction center that contains chlorophyll a and then to the electron transport chain, which pumps hydrogen ions into the thylakoid interior. This action builds up a high concentration of hydrogen ions. The hydrogen ions flow through ATP synthase during chemiosmosis to form molecules of ATP, which are used for the formation of sugar molecules in the second stage of photosynthesis. Photosystem I absorbs a second photon, which results in the formation of an NADPH molecule, another energy and reducing carrier for the light-independent reactions.

Visual Connection Questions

(Figure) What is the source of electrons for the chloroplast electron transport chain?

  1. Water
  2. Oxygen
  3. Carbon dioxide
  4. NADPH

Review Questions

Which of the following structures is not a component of a photosystem?

  1. ATP synthase
  2. antenna molecule
  3. reaction center
  4. primary electron acceptor

A

How many photons does it take to fully reduce one molecule of NADP+ to NADPH?

  1. 1
  2. 2
  3. 4
  4. 8

B

Which complex is not involved in the establishment of conditions for ATP synthesis?

  1. photosystem I
  2. ATP synthase
  3. photosystem II
  4. cytochrome complex

C

From which component of the light-dependent reactions does NADPH form most directly?

  1. photosystem II
  2. photosystem I
  3. cytochrome complex
  4. ATP synthase

B

Three of the same species of plant are each grown under a different colored light for the same amount of time. Plant A is grown under blue light, Plant B is grown under green light, and Plant C is grown under orange light. Assuming the plants use only chlorophyll a and chlorophyll b for photosynthesis, what would be the predicted order of the plants from most growth to least growth?

  1. A, C, B
  2. A, B, C
  3. C, A, B
  4. B, A, C

A

Plants containing only chlorophyll b are exposed to radiation with the following wavelengths: 10nm (x-rays), 450nm (blue light), 670nm (red light), and 800nm (infrared light). Which plants harness the most energy for photosynthesis?

  1. X-ray irradiated plants
  2. Blue light irradiated plants
  3. Red light irradiated plants
  4. Infrared irradiated plants

B

Critical Thinking Questions

Describe the pathway of electron transfer from photosystem II to photosystem I in light-dependent reactions.

A photon of light hits an antenna molecule in photosystem II, and the energy released by it travels through other antenna molecules to the reaction center. The energy causes an electron to leave a molecule of chlorophyll a to a primary electron acceptor protein. The electron travels through the electron transport chain and is accepted by a pigment molecule in photosystem I.

What are the roles of ATP and NADPH in photosynthesis?

Both of these molecules carry energy; in the case of NADPH, it has reducing power that is used to fuel the process of making carbohydrate molecules in light-independent reactions.

How and why would the end products of photosynthesis be changed if a plant had a mutation that eliminated its photosystem II complex?

Knocking out photosystem II would eliminate the production of oxygen and ATP during photosynthesis. Photosystem II splits water into oxygen atoms, hydrogen protons that remain in the thylakoid lumen, and hydrogen-derived electrons that move from the reaction center into the electron transport chain. The transfer of an electron through the electron transport chain provides the energy to pump more protons into the thylakoid lumen to maintain a higher concentration of protons there. Moving protons across the thylakoid membrane back to the stroma provides the energy for ATP synthase to produce ATP. Without this proton gradient, ATP will not be synthesized.

Glossary

absorption spectrum
range of wavelengths of electromagnetic radiation absorbed by a given substance
antenna protein
pigment molecule that directly absorbs light and transfers the energy absorbed to other pigment molecules
carotenoid
photosynthetic pigment (yellow-orange-red) that functions to dispose of excess energy
chlorophyll a
form of chlorophyll that absorbs violet-blue and red light and consequently has a bluish-green color; the only pigment molecule that performs the photochemistry by getting excited and losing an electron to the electron transport chain
chlorophyll b
accessory pigment that absorbs blue and red-orange light and consequently has a yellowish-green tint
cytochrome complex
group of reversibly oxidizable and reducible proteins that forms part of the electron transport chain between photosystem II and photosystem I
electromagnetic spectrum
range of all possible frequencies of radiation
electron transport chain
group of proteins between PSII and PSI that pass energized electrons and use the energy released by the electrons to move hydrogen ions against their concentration gradient into the thylakoid lumen
light harvesting complex
complex that passes energy from sunlight to the reaction center in each photosystem; it consists of multiple antenna proteins that contain a mixture of 300 to 400 chlorophyll a and b molecules as well as other pigments like carotenoids
P680
reaction center of photosystem II
P700
reaction center of photosystem I
photoact
ejection of an electron from a reaction center using the energy of an absorbed photon
photon
distinct quantity or “packet” of light energy
photosystem
group of proteins, chlorophyll, and other pigments that are used in the light-dependent reactions of photosynthesis to absorb light energy and convert it into chemical energy
photosystem I
integral pigment and protein complex in thylakoid membranes that uses light energy to transport electrons from plastocyanin to NADP+ (which becomes reduced to NADPH in the process)
photosystem II
integral protein and pigment complex in thylakoid membranes that transports electrons from water to the electron transport chain; oxygen is a product of PSII
primary electron acceptor
pigment or other organic molecule in the reaction center that accepts an energized electron from the reaction center
reaction center
complex of chlorophyll molecules and other organic molecules that is assembled around a special pair of chlorophyll molecules and a primary electron acceptor; capable of undergoing oxidation and reduction
spectrophotometer
instrument that can measure transmitted light and compute the absorption
wavelength
distance between consecutive points of equal position (two crests or two troughs) of a wave in a graphic representation; inversely proportional to the energy of the radiation

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The Light-Dependent Reactions of Photosynthesis by OpenStax Biology 2nd Edition is licensed under a Creative Commons Attribution 4.0 International License, except where otherwise noted.

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