bioluminescence(redirected from Bioluminance)
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bioluminescence(bī'ōlo͞o'mĭnĕs`əns), production of light by living organisms. Organisms that are bioluminescent include certain fungi and bacteria that emit light continuously. The dinoflagellates, a group of marine algae, produce light only when disturbed. Bioluminescent animals include such organisms as ctenophores, annelid worms, mollusks, insects such as fireflies, and fish. The production of light in bioluminescent organisms results from the conversion of chemical energy to light energy. In fireflies, one type of a group of substances known collectively as luciferin combines with oxygen to form an oxyluciferin in an excited state, which quickly decays, emitting light as it does. The reaction is mediated by an enzyme, luciferase, which is normally bound to ATP (see adenosine triphosphateadenosine triphosphate
(ATP) , organic compound composed of adenine, the sugar ribose, and three phosphate groups. ATP serves as the major energy source within the cell to drive a number of biological processes such as photosynthesis, muscle contraction, and the synthesis of
..... Click the link for more information. ) in an inactive form. When the signal for the specialized bioluminescent cells to flash is receive, the luciferase is liberated from the ATP, causes the luciferin to oxidize, and then somehow recombines with ATP. Different organisms produce different bioluminescent substances. Bioluminescent fish are common in ocean depths; the light probably aids in species recognition in the darkness. Other animals seem to use luminescence in courtship and mating and to divert predators or attract prey.
The emission of light by living organisms that is visible to other organisms. The enzymes and other proteins associated with bioluminescence have been developed and exploited as markers or reporters of other biochemical processes in biomedical research. Bioluminescence provides a unique tool for investigating and understanding numerous basic physiological processes, both cellular and organismic.
Although rare in terms of the total number of luminous species, bioluminescence is phylogenetically diverse, occurring in many different groups (see table). Luminescence is unknown in higher plants and in vertebrates above the fishes, and is also absent in several invertebrate phyla. In some phyla or taxa, a substantial proportion of the genera are luminous (for example, ctenophores, about 50%; cephalopods, greater than 50%). Commonly, all members of a luminous genus emit light, but in some cases there are both luminous and nonluminous species.
|Group||Features of luminous displays|
|Bacteria||Organisms glow constantly; system is autoinduced|
|Fungi||Mushrooms and mycelia produce constant dim glow|
|Dinoflagellates||Flagellated algae flash when disturbed|
|Coelenterates||Jellyfish, sea pansies, and comb jellies emit flashes|
|Annelids||Marine worms and earthworms exude luminescence|
|Mollusks||Squid and clams exude luminous clouds; also have|
|Crustacea||Shrimp, copepods, ostracodes; exude luminescence;|
|also have photophores|
|Insects||Fireflies (beetles) emit flashes; flies (Diptera) glow|
|Echinoderms||Brittle stars emit trains of rapid flashes|
|Fish||Many bony and cartilaginous fish are luminous;|
|some use symbiotic bacteria; others are self-|
|luminous; some have photophores|
Bioluminescence is most prevalent in the marine environment; it is greatest at midocean depths, where some daytime illumination penetrates. In these locations, bioluminescence may occur in over 95% of the individuals. Where high densities of luminous organisms occur, their emissions can exert a significant influence on the communities and may represent an important component in the ecology, behavior, and physiology of the latter. Above and below midocean depths, luminescence decreases to less than 10% of all individuals and species; among coastal species, less than 2% are bioluminescent. Firefly displays of bioluminescence are among the most spectacular, but bioluminescence is rare in the terrestrial environment. Other terrestrial luminous forms include millipedes, centipedes, earthworms, and snails, but the display in these is not very bright.
While not metabolically essential, light emission can confer an advantage on the organism. The light can be used in diverse ways. Most of the perceived functions of bioluminescence fall into four categories: defense, offense, communication, and dispersal to enhance propagation.
Bioluminescence does not come from or depend on light absorbed by the organism. It derives from an enzymatically catalyzed chemiluminescence, a reaction in which the energy released is transformed into light energy. One of the reaction intermediates or products is formed in an electronically excited state, which then emits a photon.
Bioluminescence originated and evolved independently many times, and is thus not an evolutionarily conserved function. It has been estimated that present-day luminous organisms come from as many as 30 different evolutionarily distinct origins. In the different groups of organisms, the genes and proteins involved are unrelated, and it may be confusing that the substrates and enzymes, though chemically different, are all referred to as luciferin and luciferase, respectively. To be correct and specific, each should be identified with the organism.
Luminous bacteria typically emit a continuous light, usually blue-green. When strongly expressed, a single bacterium may emit 104 or 105 photons per second. A primary habitat where most species abound is in association with another (higher) organism, dead or alive, where growth and propagation occur. Luminous bacteria are ubiquitous in the oceans and can be isolated from most seawater samples. The most exotic specific associations involve specialized light organs (for example, in fish and squid) in which a pure dense culture of luminous bacteria is maintained. In teleost fishes, 11 different groups carrying such bacteria are known, an exotic example being the flashlight fish.
Of the approximately 70,000 insect genera, only about 100 are classed as luminous. But their luminescence is impressive, especially in the fireflies and their relatives. Fireflies possess ventral light organs on posterior segments; the South American railroad worm, Phrixothrix, has paired green lights on the abdominal segments and red head lights; while the click and fire beetles, Pyrophorini, have both running lights (dorsal) and landing lights (ventral). The dipteran cave glow worm, in a different group and probably different biochemically, exudes beaded strings of slime from its ceiling perch, serving to entrap minute flying prey, which are attracted by the light emitted by the animal. The major function of light emission in fireflies is for communication during courtship, typically involving the emission of a flash by one sex as a signal, to which the other sex responds, usually in a species-specific pattern. The time delay between the two may be a signaling feature; for example, it is precisely 2 s in some North America species. But the flashing pattern is also important in some cases, as is the kinetic character of the individual flash (duration; onset and decay kinetics).
The firefly system was the first in which the biochemistry was characterized. In 1947 it was discovered that adenosine triphosphate (ATP) functions to form a luciferyl adenylate intermediate from firefly luciferin. This then reacts with oxygen to form a cyclic luciferyl peroxy species, which breaks down to yield CO2 and an excited state of the carbonyl product (thus emitting a photon). Luciferase catalyzes both the reaction of luciferin with ATP and the subsequent steps leading to the excited product.
Bioluminescence and chemiluminescence have come into widespread use for quantitative determinations of specific substances in biology and medicine. Luminescent tags have been developed that are as sensitive as radioactivity, and now replace radioactivity in many assays. The biochemistry of different luciferase systems is different, so many different substances can be detected. One of the first, and still widely used, assays involves the use of firefly luciferase for the detection of ATP. The amount of oxygen required for bioluminescence in luminescent bacteria is small, and therefore the reaction readily occurs. Luminous bacteria can be used as a very sensitive test for oxygen, sometimes in situations where no other method is applicable. An oxygen electrode incorporating luminous bacteria has been developed.
Luciferases have also been exploited as reporter genes for many different purposes. Analytically, such systems are virtually unique in that they are noninvasive and nondestructive: the relevant activity can be measured as light emission in the intact cell and in the same cell over the course of time. Examples of the use of luciferase genes are the expression of firely and bacterial luciferases under the control of circadian promoters; and the use of coelenterate luciferase expressed transgenically (in other organisms) to monitor calcium changes in living cells over time. Green fluorescent protein is widely used as a reporter gene for monitoring the expression of some other gene under study, and for how the expression may differ, for example at different stages of development or as the consequence of some experimental procedure.
the visible luminescence of organisms arising during their life processes. It occurs in several dozen species of bacteria, lower plants (fungi), some invertebrates (from protozoans to insects inclusive), and fish. Bioluminescence is more widespread among inhabitants of the seas and oceans, where luminescent organisms sometimes multiply in such numbers as to cause the sea to glow. It is constant and continuous in many organisms (such as bacteria, protozoans, crustaceans, and fungi) if oxygen is present in the environment. In other organisms it occurs in separate flashes and depends on physiological conditions (such as hunger, period of reproduction, and so on). The biological role of luminescence varies. For example, in luminescent insects it serves as a signal enabling males and females to find each other. In a number of deep-sea fishes it is used to illuminate and attract prey, whereas the cuttlefish protects itself from predators by ejecting a luminescent fluid, and so on. Many animals have complex organ structures for luminescence. In some cases luminescent bacteriasymbionts (for example, the so-called nonindependent luminescence of several fishes) are the source of an animal’s bioluminescence.
In terms of its mechanism, bioluminescence is a form of chemoluminescence. Luminescence occurs during enzymic oxidation by atmospheric oxygen of specific substances called luciferins. By releasing chemical energy some of the luciferin molecules become excited and, on returning to their basic state, emit light. Luciferins, like enzymes (luciferases) which catalyze their oxidation, differ in organisms of various species. For example, the luciferin in bacteria is flavine mononucleotide (riboflavin-5-phosphate), a coenzyme of several oxidation-reduction enzymes. A common property of all the luciferins is their ability to produce intense fluorescence. When isolated in crystalline form, luciferin can also be oxidized chemically, but this process differs from enzymic oxidation in releasing energy as heat and not as quanta of light.
Three systems of bioluminescence are distinguished according to their degree of complexity. The simplest, which consists solely of luciferin and luciferase, occurs in Cypridina (this crustacean emits a blue-green light with a maximum wavelength of 440 to 460 nanometers [nm]), in the fish Argon, and in other organisms. The system is more complex in bacteria in which, in addition to luciferin and luciferase, there is a long-chain aldehyde—a compound of the type , where R is the direct hydrocarbon chain containing seven to 14 carbon atoms. The simplified scheme of the reaction of bioluminescence in this case has the following form: FMN · H2 + ½O2 + E + R · CHO → FMN + H2O + reaction products + light. (FMN is the oxidized form of flavine mononucleotide, FMN · H2 is its reduced form, and E is the enzyme luciferase.) The bacteria emit a green light with a maximum wavelength of about 560 nanometers (nm). Bioluminescence is most complex in insects, such as the firefly. Its organs emit yellow-green flashes of light (about 560 nm) caused by nerve impulses. Besides luciferin and luciferase, the insect needs ATP (adenosine triphosphate) and magnesium for bioluminescence. The energy released during the hydrolysis of ATP apparently stimulates the luciferinluciferase system and ensures the oxidation of luciferin with the emission of light. The system does not function in the absence of ATP.
It is assumed (by the American scientist W. D. McElroy et al, 1962) that bioluminescence developed during the transition from anaerobic forms of life to aerobic forms, that is, when oxygen began to accumulate in the primordial earth’s atmosphere. Oxygen was probably toxic to the anaerobic organisms existing at that time, and it was taken up by organisms capable of reducing it quickly. In the process, the release of energy in the form of light was sometimes more advantageous than in the form of heat. In bioluminescent protozoans, the energy liberated during the oxidation of substrates was released in the form of light or heat; that is, it was lost without benefiting the organism. Therefore, in the course of further evolution those organisms gained an advantage in which the mechanism of energy accumulation developed. When these forms appeared, oxidative luminescent reactions were no longer beneficial in natural selection, and they even became injurious. However, as a result of secondary evolutionary processes, bioluminescence was able to be preserved as a rudimentary character in individual, unrelated groups of organisms in which it acquired different functions, such as the sex signal in fireflies.
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McElroy, W. D., and H. H. Seliger. “Proiskhozhdenie i evoliutsiia bioluminestsentsii.” In the book Gorizonty biokhimii. Moscow, 1965. (Translated from English.)
Bioliuminestsentsiia [collection of articles]. Moscow, 1965.
Bioenergetika i biologicheskaia spektrofotometriia. Moscow, 1967.
L. A. TUMERMAN