- Key People:
- Leopold Ružička
- Henry Edward Armstrong
- Otto Wallach
- Related Topics:
- diterpene
- camphene
- isopulegol
- citronellol
- citronellal
Isoprenoid
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What are isoprenoids?
Isoprenoids are a class of organic compounds composed of hydrocarbon units, with each unit containing five carbon atoms arranged in a specific pattern. They play various physiological roles in plants and animals and have commercial applications.
In living organisms, isoprenoids function as pigments, fragrances, vitamins, and precursors to sex hormones. Rubber is a polyisoprene, and some isoprenoids are used as flavorings, solvents, and raw materials for chemicals.
Isoprenoids have a five-carbon building block called isoprene. Terpene refers to naturally occurring compounds that derive from a single isoprene unit, but the terms terpenes and isoprenoids are now used interchangeably.
Isoprenoids are classified by the number of isoprene units they contain. The smallest terpene molecules are monoterpenes, and larger molecules are sesquiterpenes, diterpenes, triterpenes, and tetraterpenes.
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What is the basic building block of isoprenoids?
The basic building block of isoprenoids is a five-carbon hydrocarbon unit called isoprene (2-methyl-1,3-butadiene). Isoprene is a branched-chain unsaturated hydrocarbon with two carbon-carbon double bonds.
Isoprenoids contain two to many thousands of isoprene units and may have functional chemical groups attached to their carbon backbone, contributing to their diversity. Isoprenoids play many roles in plants and animals, from pigments and fragrances to vitamins and hormone precursors. They also have commercial uses as flavorings, solvents, and raw materials for chemicals.
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Where are isoprenoids found in nature?
Isoprenoids are found widely in plants and animals and have a variety of physiological and commercial roles.
In plants, isoprenoids are present in essential oils, gummy exudates (oleoresins and latices), and contribute to growth, pigments, and certain alkaloids. In animals, they constitute oily or waxy substances like fish liver oils, wool wax, and pigments in egg yolk, butterfat, feathers, and fish scales. They also play vital roles in metabolic processes in animals, such as vitamin A production, blood clotting, and energy derivation.
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What roles do isoprenoids play in plants and animals?
Isoprenoids play diverse roles in plants and animals. In plants, they are found in essential oils and contribute to growth via hormones like gibberellic acid. They also contribute to pigments such as carotenoids and are partly present in chlorophyll, which is essential for photosynthesis. Some isoprenoids may attract certain insects and repel others, defend the plant, or act as wound-sealing agents.
In animals, isoprenoids include oily or waxy substances like fish liver oils and pigments in egg yolk. Carotenoid pigments are a source of vitamin A, which is essential for vision, growth, and neural development. Other vitamins that are isoprenoids include vitamin E, which is important in reproduction, and vitamin K, which is necessary for blood clotting. Additionally, isoprenoids influence maturation and mating behavior in insects and mark the way between the nest and sources of food.
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How are isoprenoids classified into different groups?
Isoprenoids are classified into groups based on the number of isoprene units they contain. Isoprene is a hydrocarbon with five carbon atoms. The different classes of isoprenoids include:
* Monoterpenes Two isoprene units (C10H16)
* Sesquiterpenes Three isoprene units (C15H24)
* Diterpenes Four isoprene units (C20H32)
* Triterpenes Six isoprene units (C30H48)
* Tetraterpenes Eight isoprene units (C40H64)
* Polyterpenes Many isoprene units (C5H8)nThese units link "head to tail," where carbon atom 1 of one unit bonds to carbon atom 4 of the next. Additional bonds can create monocyclic, bicyclic, and other subclasses with rings.
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What are some important products made from isoprenoids in industry or medicine?
Isoprenoids have diverse applications across industries and medicine. They are used as ingredients in perfumes and incense, as flavorings and spices, and in varnishes and medicinals. Rubber is a polyterpene hydrocarbon found in the latices of plants. Rosin, often chemically modified, is used in coating materials and inexpensive soaps. Turpentine, once a solvent, now provides components for chemical processes, including lubricant additives, vitamin A, insecticides, resins in adhesives, and perfume ingredients.
In animals, isoprenoids are the source of vitamin A, vitamin E, and vitamin K. Certain isoprenoid substances influence maturation and mating behavior in insects. Scientists also believe that drugs blocking protein prenylation (the addition of isoprenoids to proteins) can prevent cancer spread.
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Isoprenoid, any of a class of organic compounds composed of two or more units of hydrocarbons, with each unit consisting of five carbon atoms arranged in a specific pattern. Isoprenoids play widely varying roles in the physiological processes of plants and animals. They also have a number of commercial uses.
Isoprenoids in living organisms range in function from pigments and fragrances to vitamins and precursors of sex hormones. One of the most familiar natural substances, rubber, is a polyisoprene. Other commercially valuable isoprenoids are those used as flavourings, solvents, and raw materials for chemicals.
The five-carbon unit that constitutes the basic building block of isoprenoids is a hydrocarbon called isoprene. Isoprene (2-methyl-1,3-butadiene) is a branched-chain unsaturated hydrocarbon, unsaturated meaning it contains one or more double bonds between carbon atoms. Isoprene has in fact two carbon-carbon double bonds. Isoprenoids contain from two to many thousands of isoprene units. The carbon backbone of an isoprenoid can have one or more functional chemical groups, such as hydroxyl and carbonyl, attached to it. These contribute to the diversity of isoprenoids.
The name terpene specifically refers to naturally occurring compounds that are derivatives of a single isoprene unit, but modern usage has become less precise, and the terms terpenes and isoprenoids are used interchangeably. The word terpene comes from an older spelling of turpentine (terpentine), a cleaner that is a mixture of isoprenoids (originally the resin of the terebinth plant).
The smallest terpene molecules—those containing 10 carbon atoms—are called monoterpenes. The larger molecules, increased by one isoprene unit at a time, are called sesquiterpenes, diterpenes, triterpenes, and tetraterpenes, respectively (see below Isoprenoid compounds). The monoterpenes are mostly volatile, which accounts for their fragrances. Terpenes of higher molecular weight are less volatile, although sesquiterpenes contribute to the flavours of some foods.
Isoprenoids of plants and animals
In plants, isoprenoids occur in the essential oils, which are found in the gummy exudates (oleoresins and latices) of many trees and shrubs. Plant isoprenoids effect growth (e.g., the hormone gibberellic acid) and contribute to red, yellow, and orange pigments (carotenoids). Chlorophyll, the green pigment essential in photosynthesis, is partly isoprenoid, as are certain alkaloids, nitrogen-containing compounds present in many plants. In animals, isoprenoids comprise various oily or waxy substances such as fish liver oils, wool wax, and the yellow pigments in egg yolk, butterfat, feathers, and fish scales.
Isoprenoids are not uniformly distributed among plants or animals, but certain classes of these compounds are typical of broad groups of tissues. For example, the nonvolatile substances present in resins produced by trees of the pine family contain diterpene carboxylic acids belonging to three types: abietic, palustric, and elliotinoic. The latices of a few species of plants contain the polyterpene hydrocarbons rubber or gutta-percha. Certain other species, including related species, of plants may be characterized by the presence of menthol, citral, camphor, limonene, or α-pinene.
The role of the monoterpenes and sesquiterpenes produced by plants has not been established, although it has been suggested that they attract certain insects and repel others. Certain plants produce isoprenoids that are very similar to hormones involved in the development of insects that prey on those plants; the plant substances prevent the maturation of the insect, thus serving to defend the plant. The rosin acids of pine trees and the rubber and gutta-percha in latices of various plants may serve as wound-sealing agents.
Several isoprenoids are vitally important in metabolic processes in animals. Tetraterpene carotenoid pigments are the source of vitamin A, which is essential for vision and is involved in growth, reproductive function, and neural development in animals. Other vitamins that are wholly or partly isoprenoid include vitamin E, important in reproduction, and vitamin K, necessary for the blood-clotting process. The ubiquinones (coenzyme Q), which are involved in the derivation of energy by the oxidation of food, are also formed from isoprenoids. The livers of fishes and other animals are particularly rich in oils that are largely acyclic triterpenoid hydrocarbons, especially squalene. In insects, certain isoprenoid substances influence maturation and mating behaviour, communicate alarm or repel predators, or mark the way between the nest and sources of food.
In the 1980s scientists discovered that proteins in animals often have isoprenoid structures containing 15 or 20 carbon atoms attached to a particular side chain of the protein. The isoprenoid is added after the protein is otherwise complete. The so-called prenylated proteins do not function without the isoprenoid. These modifications occur in proteins that induce cancers, and scientists believe that drugs that block protein prenylation can be a means to prevent the spread of the disease in an individual.
Steroids, a class of compounds of great importance in both plants and animals, are not isoprenoids but are derived directly from them.
Uses of isoprenoids
Of the uses that humans have found for isoprenoids, many were established in antiquity—as ingredients of perfumes and incense, flavourings and spices, and varnishes and medicinals. Amber, a fossilized isoprenoid resin, has been prized as a gemstone since prehistoric times. Rubber was used by the Central and South American Indians before the Spanish conquest.
Modern applications of isoprenoids are extremely diverse. Turpentine, long employed as a solvent, is used mostly as a source of its individual components, which are raw materials for chemical processing. Products derived from turpentine include ingredients for perfumes, vitamin A, lubricant additives, insecticides, resins used in adhesives, and industrial chemicals. Rosin, usually modified by chemical treatment, is widely used to make inexpensive soaps and coating materials. Other isoprenoids that are valuable in industry and commerce include camphor, menthol, citronella oil, and natural rubber.

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