Many terpenes are derived commercially from conifer resins, such as those made by this pine.
Terpenes () are a large and diverse class of organic compounds, produced by a variety of plants, particularly conifers,[1] and by some insects such as termites or swallowtail butterflies, which emit terpenes from their osmeteria. They often have a strong odor and may protect the plants that produce them by deterring herbivores and by attracting predators and parasites of herbivores.[2][3] The difference between terpenes and terpenoids is that terpenes are hydrocarbons, whereas terpenoids contain additional functional groups.
They are the major components of resin, and of turpentine produced from resin. The name "terpene" is derived from the word "terpentine", an obsolete form of the word "turpentine". In addition to their roles as end-products in many organisms, terpenes are also major biosynthetic building blocks within nearly every living creature. Steroids, for example, are derivatives of the triterpene squalene.
When terpenes are modified chemically, such as by oxidation or rearrangement of the carbon skeleton, the resulting compounds are generally referred to as terpenoids. Some authors will use the term terpene to include all terpenoids. Terpenoids are also known as isoprenoids.
Terpenes and terpenoids are the primary constituents of the essential oils of many types of medicinal plants and flowers. Essential oils are used widely as fragrances in perfumery, and in medicine and alternative medicines such as aromatherapy. Synthetic variations and derivatives of natural terpenes and terpenoids also greatly expand the variety of aromas used in perfumery and flavors used in food additives. Vitamin A is a terpenoid.
Higher amounts of terpenes are released by trees in warmer weather, acting as a natural form of cloud seeding. The clouds reflect sunlight, allowing the forest temperature to regulate.[4] The aroma and flavor of hops comes, in part, from sesquiterpenes (mainly alpha-humulene and beta-caryophyllene), which affect beer quality.[5] Terpenes are also major constituents of Cannabis sativa plants, which contain at least 120 identified compounds.[6]
Contents
- 1 Structure and biosynthesis
- 2 Types
- 3 Properties
- 4 References
- 5 External links
Structure and biosynthesis
Terpenes are derived biosynthetically from units of isoprene, which has the molecular formula C5H8. The basic molecular formula of terpenes are multiples of that, (C5H8)n where n is the number of linked isoprene units. This is called the biogenetic isoprene rule or the C5 rule. In 1953, Leopold Ružička discovered that the isoprene units may be linked together "head to tail" to form linear chains or they may be arranged to form rings.[7] One can consider the isoprene unit as one of nature's common building blocks. As chains of isoprene units accumulate, the resulting terpenes are classified sequentially by size as hemiterpenes, monoterpenes, sesquiterpenes, diterpenes, sesterterpenes, triterpenes, and tetraterpenes, all synthesized by terpene synthase.[8][9]
Isoprene itself does not undergo the building process, but rather activated forms, isopentenyl pyrophosphate (IPP or also isopentenyl diphosphate) and dimethylallyl pyrophosphate (DMAPP or also dimethylallyl diphosphate), are the components in the biosynthetic pathway. IPP is formed from acetyl-CoA via the intermediacy of mevalonic acid in the HMG-CoA reductase pathway. An alternative, totally unrelated biosynthesis pathway of IPP is known in some bacterial groups and the plastids of plants, the so-called MEP(2-Methyl-D-erythritol-4-phosphate)-pathway, which is initiated from C5-sugars. In both pathways, IPP is isomerized to DMAPP by the enzyme isopentenyl pyrophosphate isomerase.
Isopentenyl pyrophosphate
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Dimethylallyl pyrophosphate
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Types
Second- or third-instar caterpillars of
Papilio glaucus emit terpenes from their osmeterium.
Terpenes may be classified by the number of isoprene units in the molecule; a prefix in the name indicates the number of terpene units needed to assemble the molecule.
- Hemiterpenes consist of a single isoprene unit. Isoprene itself is considered the only hemiterpene, but oxygen-containing derivatives such as prenol and isovaleric acid are hemiterpenoids.
- Monoterpenes consist of two isoprene units and have the molecular formula C10H16. Examples of monoterpenes and monoterpenoids include geraniol, terpineol (present in lilacs), limonene (present in citrus fruits), myrcene (present in hops), linalool (present in lavender) or pinene (present in pine trees).[10] Iridoids derive from monoterpenes.
- Sesquiterpenes consist of three isoprene units and have the molecular formula C15H24. Examples of sesquiterpenes and sesquiterpenoids include humulene, farnesenes, farnesol. (The sesqui- prefix means one and a half.)
- Diterpenes are composed of four isoprene units and have the molecular formula C20H32. They derive from geranylgeranyl pyrophosphate. Examples of diterpenes and diterpenoids are cafestol, kahweol, cembrene and taxadiene (precursor of taxol). Diterpenes also form the basis for biologically important compounds such as retinol, retinal, and phytol.
- Sesterterpenes, terpenes having 25 carbons and five isoprene units, are rare relative to the other sizes. (The sester- prefix means half to three, i.e. two and a half.) An example of a sesterterpenoid is geranylfarnesol.
- Triterpenes consist of six isoprene units and have the molecular formula C30H48. The linear triterpene squalene, the major constituent of shark liver oil, is derived from the reductive coupling of two molecules of farnesyl pyrophosphate. Squalene is then processed biosynthetically to generate either lanosterol or cycloartenol, the structural precursors to all the steroids.
- Sesquarterpenes are composed of seven isoprene units and have the molecular formula C35H56. Sesquarterpenes are typically microbial in their origin. Examples of sesquarterpenoids are ferrugicadiol and tetraprenylcurcumene.
- Tetraterpenes contain eight isoprene units and have the molecular formula C40H64. Biologically important tetraterpenoids include the acyclic lycopene, the monocyclic gamma-carotene, and the bicyclic alpha- and beta-carotenes.
- Polyterpenes consist of long chains of many isoprene units. Natural rubber consists of polyisoprene in which the double bonds are cis. Some plants produce a polyisoprene with trans double bonds, known as gutta-percha.
- Norisoprenoids, such as the C13-norisoprenoids 3-oxo-α-ionol present in Muscat of Alexandria leaves and 7,8-dihydroionone derivatives, such as megastigmane-3,9-diol and 3-oxo-7,8-dihydro-α-ionol found in Shiraz leaves (both grapes in the species Vitis vinifera)[11] or wine[12][13] (responsible for some of the spice notes in Chardonnay), can be produced by fungal peroxidases[14] or glycosidases.[15]
Properties
Terpenes have desirable properties for use in food, cosmetics, pharmaceutical and biotechnology industries.[16][17]
The complex structure of many terpenes often makes their chemical synthesis difficult, and the extraction from plants is also difficult and time-consuming, and yields only small amounts. The genomes of 17 plant species contain genes that encode terpenoid synthase enzymes imparting terpenes with their basic structure, and cytochrome P450s that modify this basic structure.[18]
Terpenes have properties that make them useful active ingredients as part of natural agricultural pesticides.[19] Terpenes are used by termites of the Nasutitermitinae family to ward off predatory insects, through the use of a specialized mechanism called a fontanellar gun.[20]
References
- ^ Merriam-Webster Online Dictionary
- ^ Martin, Diane M.; Gershenzon, Jonathan; Bohlmann, Jörg (July 2003). "Induction of Volatile Terpene Biosynthesis and Diurnal Emission by Methyl Jasmonate in Foliage of Norway Spruce". Plant Physiology. 132 (3): 1586–1599. doi:10.1104/pp.103.021196. Retrieved 1 November 2014.
- ^ Pichersky, E. (10 February 2006). "Biosynthesis of Plant Volatiles: Nature's Diversity and Ingenuity". Science. 311 (5762): 808–811. Bibcode:2006Sci...311..808P. doi:10.1126/science.1118510. PMC 2861909 . PMID 16469917.
- ^ Adam, David (October 31, 2008). "Scientists discover cloud-thickening chemicals in trees that could offer a new weapon in the fight against global warming". The Guardian.
- ^ Steenackers, B; De Cooman, L; De Vos, D (2015). "Chemical transformations of characteristic hop secondary metabolites in relation to beer properties and the brewing process: A review". Food Chemistry. 172: 742–56. doi:10.1016/j.foodchem.2014.09.139. PMID 25442616.
- ^ Andre CM+, Hausman JF, Guerriero G (2016). "Cannabis sativa: The Plant of the Thousand and One Molecules". Front Plant Sci. 7: 19. doi:10.3389/fpls.2016.00019. PMC 4740396 . PMID 26870049.
- ^ Ružička, Leopold (1953). "The isoprene rule and the biogenesis of terpenic compounds". Cellular and Molecular Life Sciences. 9 (10): 357–367. doi:10.1007/BF02167631.
- ^ Kumari, I; Ahmed, M; Akhter, Y (2017). "Evolution of catalytic microenvironment governs substrate and product diversity in trichodiene synthase and other terpene fold enzymes". Biochimie. 144: 9. doi:10.1016/j.biochi.2017.10.003. PMID 29017925.
- ^ Pazouki, L; Niinemets, Ülo (2016). "Multi-Substrate Terpene Synthases: Their Occurrence and Physiological Significance". Frontiers in Plant Science. 7: 1019. doi:10.3389/fpls.2016.01019. PMC 4940680 . PMID 27462341.
- ^ Eberhard Breitmaier (2006). Terpenes: Flavors, Fragrances, Pharmaca, Pheromones. John Wiley & Sons. pp. 1–13. ISBN 3527317864.
- ^ Günata, Ziya; Wirth, Jérémie L.; Guo, Wenfei; Baumes, Raymond L. (2001). "Carotenoid-Derived Aroma Compounds; chapter 13: Norisoprenoid Aglycon Composition of Leaves and Grape Berries from Muscat of Alexandria and Shiraz Cultivars". ACS Symposium Series. ACS Symposium Series. 802: 255–261. doi:10.1021/bk-2002-0802.ch018. ISBN 0-8412-3729-8. , ACS Symposium Series, Vol. 802
- ^ Winterhalter, P.; Sefton, M. A.; Williams, P. J. (1990). "Volatile C13-Norisoprenoid Compounds in Riesling Wine Are Generated From Multiple Precursors". Am. J. Enol. Vitic. 41 (4): 277–283.
- ^ Vinholes, Juliana; Coimbra, Manuel A.; Rocha, Sílvia M. (2009). "Rapid tool for assessment of C13 norisoprenoids in wines". Journal of Chromatography A. 1216 (47): 8398–403. doi:10.1016/j.chroma.2009.09.061. PMID 19828152.
- ^ Zelena, Kateryna; Hardebusch, Björn; HüLsdau, BäRbel; Berger, Ralf G.; Zorn, Holger (2009). "Generation of Norisoprenoid Flavors from Carotenoids by Fungal Peroxidases". Journal of Agricultural and Food Chemistry. 57 (21): 9951–5. doi:10.1021/jf901438m. PMID 19817422.
- ^ Cabaroglu, Turgut; Selli, Serkan; Canbas, Ahmet; Lepoutre, Jean-Paul; Günata, Ziya (2003). "Wine flavor enhancement through the use of exogenous fungal glycosidases". Enzyme and Microbial Technology. 33 (5): 581–587. doi:10.1016/S0141-0229(03)00179-0.
- ^ Thimmappa, R.; Geisler, K.; Louveau, T.; O’Maille, P.; Osbourn, A. (2014). "Triterpene biosynthesis in plants". Annu Rev Plant Biol. 65: 225–57. doi:10.1146/annurev-arplant-050312-120229. PMID 24498976.
- ^ Augustin, J.M.; Kuzina, V.; Andersen, S.B.; Bak, S. (2011). "Molecular activities, biosynthesis and evolution of triterpenoid saponins". Phytochemistry. 72 (6): 435–57. doi:10.1016/j.phytochem.2011.01.015. PMID 21333312. Retrieved 19 January 2015.
- ^ Boutanaev, A.M.; Moses, T.; Zi, J.; Nelson, D.R.; Mugford, S.T.; Peters, R.J.; Osbourn, A. (2015). "Investigation of terpene diversification across multiple sequenced plant genomes". Proc Natl Acad Sci USA. 112 (1): E81–8. Bibcode:2015PNAS..112E..81B. doi:10.1073/pnas.1419547112. PMC 4291660 . PMID 25502595.
- ^ Isman, MB (2000). "Plant essential oils for pest and disease management". Crop Protection. 19 (8–10): 603–608. doi:10.1016/S0261-2194(00)00079-X. Retrieved 18 September 2014.
- ^ W. L. Nutting; M. S. Blum & H. M. Fales. (1974). "Behavior of the North American Termite, Tenuirostritermes tenuirostris, with Special Reference to the Soldier Frontal Gland Secretion, Its Chemical Composition, and Use in Defense". Psyche. Hindawi Publishing Corporation. 81 (1): 167–177. doi:10.1155/1974/13854. Retrieved July 22, 2011.
External links
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Wikimedia Commons has media related to Terpenes. |
- Institute of Chemistry - terpenes
- Structures of alpha pinene and beta pinene
- Terpenes at the US National Library of Medicine Medical Subject Headings (MeSH)
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Types of Terpenes and Terpenoids (# of isoprene units)
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| Basic forms: |
- Acyclic (linear, cis and trans forms)
- Monocyclic (single ring)
- Bicyclic (2 rings)
- Iridoids (cyclopentane ring)
- Iridoid glycosides (iridoids bound to a sugar)
- Steroids (4 rings)
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| Hemiterpenoids (1) |
- Isoprene (C5H8)
- Prenol
- Isovaleric acid
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| Monoterpene (C10H16)(2) |
| Acyclic |
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| Monocyclic |
- Limonene
- Terpinene
- Phellandrene
- Umbellulone
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| Bicyclic |
- Pinene (β and α
- Camphene
- Thujene
- Sabinene
- Carene
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| Monoterpenoids (2,modified) |
| Acyclic |
- Linalool
- Citronellal
- Citral
- Citronellol
- Geraniol
- Geranyl pyrophosphate
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| Monocyclic |
- Grapefruit mercaptan
- menthol
- p-Cymene
- thymol
- Perillyl alcohol
- Carvacrol
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| Bicyclic |
- Camphor
- Borneol
- Eucalyptol
- Halomon
- Eucalyptol
- Pinene
- Ascaridole
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|
| Sesquiterpenoids (3) |
- Farnesyl pyrophosphate
- Artemisinin
- Bisabolol
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| Diterpenoids (4) |
- Geranylgeranyl pyrophosphate
- Gibberellin
- Retinol
- Retinal
- Phytol
- Taxol
- Forskolin
- Aphidicolin
- Salvinorin A
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| Sesterterpenoids (5) |
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| Triterpenoids (6) |
| Steroids |
- Phytosterols
- Campesterol
- beta Sitosterol
- gamma sitosterol
- Stigmasterol
- Tocopherols
- Cholesterol
- Testosterone
- Cholecalciferol (Vit D)
- Ecdysones
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| Other |
- Saponins
- Squalane
- Lanosterol
- Acids
- Oleanolic acid
- Ursolic acid
- Betulinic acid
- Moronic acid
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| Sesquarterpenes/oids (7) |
- ferrugicadiol
- tetraprenylcurcumene
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Tetraterpenoids
(Carotenoids) (8) |
| Carotenes |
- Alpha-Carotene
- Beta-Carotene
- Gamma-Carotene
- Delta-Carotene
- Lycopene
- Neurosporene
- Phytofluene
- Phytoene
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| Xanthophylls: |
- Canthaxanthin
- Cryptoxanthin
- Zeaxanthin
- Astaxanthin
- Lutein
- Rubixanthin
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| Polyterpenoids (many) |
- sap, resins, latex of many plants, e.g. rubber
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| Norisoprenoids (modified) |
- 3-oxo-α-ionol
- 7,8-dihydroionone
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| Synthesis |
- Terpene synthase enzymes (many), having in common a Terpene synthase N terminal domain (protein domain)
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| Activated isoprene forms |
- Isopentenyl pyrophosphate (IPP)
- Dimethylallyl pyrophosphate (DMAPP)
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Terpenes
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- Endo-Borneol
- Delta-carene
- Bornyl acetate
- α-Ylangene
- α-Copaene
- Aromadendrene
- Eremophilene
- Longifolene
- β-Guaiene
- Valencene
- β-Bisabolene
- γ-Cadinene
- β-Selinene
- Neophytadiene
- Ferruginol
- Aristolone
- β-Amyrin
- Oleanene
- Ketoursene
- α-Amyrin
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| Authority control |
- LCCN: sh85134045
- GND: 4184779-9
- NDL: 00572906
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