Jump to content

Terpene: Difference between revisions

From Wikipedia, the free encyclopedia
Browse history interactively
← Previous editNext edit →
Content deleted Content added
VisualWikitext
wl, ref
Line 15: Line 15:
==Structure and biosynthesis== <!-- This section is linked from [[Otto Wallach]] -->
==Structure and biosynthesis== <!-- This section is linked from [[Otto Wallach]] -->
[[File:Isoprene.svg|thumb|right|100px|Isoprene]]
[[File:Isoprene.svg|thumb|right|100px|Isoprene]]
Terpenes are derived biosynthetically from units of [[isoprene]], which has the molecular formula C<sub>5</sub>H<sub>8</sub>. The basic molecular formula of terpenes are multiples of that, (C<sub>5</sub>H<sub>8</sub>)<sub>n</sub> where n is the number of linked isoprene units. This is called the '''biogenetic isoprene rule''' or the ''C5 rule''. The isoprene units may be linked together "head to tail" to form linear chains or they may be arranged to form rings. One can consider the isoprene unit as one of nature's common building blocks.
Terpenes are derived biosynthetically from units of [[isoprene]], which has the molecular formula C<sub>5</sub>H<sub>8</sub>. The basic molecular formula of terpenes are multiples of that, (C<sub>5</sub>H<sub>8</sub>)<sub>n</sub> where n is the number of linked isoprene units. This is called the '''biogenetic isoprene rule''' or the ''C5 rule''. In 1953, the Croatian chemist [[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.<ref>{{cite journal |title = The isoprene rule and the biogenesis of terpenic compounds |first = Leopold |last = Ružička|journal = [[Cellular and Molecular Life Sciences]]|volume = 9|issue = 10|pages = 357–367 |year = 1953 |doi = 10.1007/BF02167631 |url=https://link.springer.com/article/10.1007%2FBF02167631}}</ref> One can consider the isoprene unit as one of nature's common building blocks.


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.
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.

Revision as of 07:56, 14 September 2017

Many terpenes are derived commercially from conifer resins, such as those made by this pine.

Terpenes (/ˈtɜːrpiːn/) 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 "turpentine". In addition to their roles as end-products in many organisms, terpenes are 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 to regulate its temperature.[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]

Structure and biosynthesis

Isoprene

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, the Croatian chemist 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.

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
Dimethylallyl pyrophosphate

As chains of isoprene units are built up, the resulting terpenes are classified sequentially by size as hemiterpenes, monoterpenes, sesquiterpenes, diterpenes, sesterterpenes, triterpenes, and tetraterpenes. Essentially, they are all synthesized by terpene synthase.

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.

Research

Terpenes have properties as chemicals in food, cosmetics, pharmaceutical and biotechnology industries.[14][15] Chemical synthesis of terpenes can be problematic because of their complex structure, and plants produce small amounts of terpenes, making it difficult, time-consuming and expensive to extract them directly from plants. 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.[16]

Research into terpenes has found that many of them possess qualities that make them useful active ingredients as part of natural agricultural pesticides.[17] 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.[18]

References

  1. ^ Merriam-Webster Online Dictionary
  2. ^ 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.
  3. ^ Pichersky, E. (10 February 2006). "Biosynthesis of Plant Volatiles: Nature's Diversity and Ingenuity". Science. 311 (5762): 808–811. doi:10.1126/science.1118510. PMC 2861909. PMID 16469917.
  4. ^ 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.
  5. ^ 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.
  6. ^ "Cannabis sativa: The Plant of the Thousand and One Molecules". Front Plant Sci. 7: 19. 2016. doi:10.3389/fpls.2016.00019. PMC 4740396. PMID 26870049. {{cite journal}}: Cite uses deprecated parameter |authors= (help)CS1 maint: unflagged free DOI (link)
  7. ^ 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.
  8. ^ Eberhard Breitmaier (2006). Terpenes: Flavors, Fragrances, Pharmaca, Pheromones. John Wiley & Sons. pp. 1–13. ISBN 3527317864.
  9. ^ 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
  10. ^ 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.
  11. ^ 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.
  12. ^ 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.
  13. ^ 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.
  14. ^ 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.
  15. ^ 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.
  16. ^ 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. doi:10.1073/pnas.1419547112. PMC 4291660. PMID 25502595.
  17. ^ 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.
  18. ^ 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. 81 (1). Hindawi Publishing Corporation: 167–177. doi:10.1155/1974/13854. Retrieved July 22, 2011. {{cite journal}}: Unknown parameter |last-author-amp= ignored (|name-list-style= suggested) (help)CS1 maint: unflagged free DOI (link)

External links

Wikimedia Commons has media related to Terpenes.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Terpene&oldid=800555746"