Sucrose, a disaccharide formed from condensation of a molecule of glucose and a molecule of fructose
Disaccharides are one of the four chemical groupings of carbohydrates (monosaccharides, disaccharides, oligosaccharides, and polysaccharides). The most common types of disaccharides—sucrose, lactose, and maltose—have 12 carbon atoms, with the general formula C12H22O11. The differences in these disaccharides are due to atomic arrangements within the molecule.[3]
The joining of monosaccharides into a double sugar happens by a condensation reaction, which involves the elimination of a water molecule from the functional groups only. Breaking apart a double sugar into its two monosaccharides is accomplished by hydrolysis with the help of a type of enzyme called a disaccharidase. As building the larger sugar ejects a water molecule, breaking it down consumes a water molecule. These reactions are vital in metabolism. Each disaccharide is broken down with the help of a corresponding disaccharidase (sucrase, lactase, and maltase).
There are two functionally different classes of disaccharides:
Reducing disaccharides, in which one monosaccharide, the reducing sugar of the pair, still has a free hemiacetal unit that can perform as a reducing aldehyde group; lactose, maltose and cellobiose are examples of reducing disaccharides, each with one hemiacetal unit, the other occupied by the glycosidic bond, which prevents it from acting as a reducing agent. They can easily be detected by the Woehlk test or Fearon's test on methylamine.[4]
Non-reducing disaccharides, in which the component monosaccharides bond through an acetal linkage between their anomeric centers. This results in neither monosaccharide being left with a hemiacetal unit that is free to act as a reducing agent. Sucrose and trehalose are examples of non-reducing disaccharides because their glycosidic bond is between their respective hemiacetal carbon atoms. The reduced chemical reactivity of the non-reducing sugars in comparison to reducing sugars, may be an advantage where stability in storage is important.[5][6]
Formation
The formation of a disaccharide molecule from two monosaccharide molecules proceeds by displacing a hydroxy group from one molecule and a hydrogen nucleus (a proton) from the other, so that the now vacant bonds on the monosaccharides join the two monomers together. Because of the removal of the water molecule from the product, the term of convenience for such a process is "dehydration reaction" (also "condensation reaction" or "dehydration synthesis"). For example, milk sugar (lactose) is a disaccharide made by condensation of one molecule of each of the monosaccharides glucose and galactose, whereas the disaccharide sucrose in sugar cane and sugar beet, is a condensation product of glucose and fructose. Maltose, another common disaccharide, is condensed from two glucose molecules.[7]
The dehydration reaction that bonds monosaccharides into disaccharides (and also bonds monosaccharides into more complex polysaccharides) forms what are called glycosidic bonds.[8]
Properties
The glycosidic bond can be formed between any hydroxy group on the component monosaccharide. So, even if both component sugars are the same (e.g., glucose), different bond combinations (regiochemistry) and stereochemistry (alpha- or beta-) result in disaccharides that are diastereoisomers with different chemical and physical properties. Depending on the monosaccharide constituents, disaccharides are sometimes crystalline, sometimes water-soluble, and sometimes sweet-tasting and sticky-feeling. Disaccharides can serve as functional groups by forming glycosidic bonds with other organic compounds, forming glycosides.
^Kwan, Lam Peng (2000). Biology- A course for O Level. p. 59. ISBN9810190964.
^Ruppersberg, Klaus; Herzog, Stefanie; Kussler, Manfred W.; Parchmann, Ilka (2019). "How to visualize the different lactose content of dairy products by Fearon's test and Woehlk test in classroom experiments and a new approach to the mechanisms and formulae of the mysterious red dyes". Chemistry Teacher International. doi:10.1515/cti-2019-0008.
^. Archived from the original on 2017-08-26. Retrieved 2010-07-21.
^"Disaccharides and Oligosaccharides". Retrieved 2008-01-29.
^Whitney, Ellie; Sharon Rady Rolfes (2011). Peggy Williams (ed.). Understanding Nutrition (Twelfth ed.). California: Wadsworth, Cengage Learning. p. 100. ISBN978-0-538-73465-3.
^"Glycosidic Link". OChemPal. Utah Valley University. Retrieved 11 December 2013.
^F.W.Parrish; W.B.Hahn, G.R.Mandels (July 1968). "Crypticity of Myrothecium verrucaria Spores to Maltose and Induction of Transport by Maltulose, a Common Maltose Contaminant". J. Bacteriol. American Society for Microbiology. 96 (1): 227–233. doi:10.1128/JB.96.1.227-233.1968. PMC252277. PMID 5690932.
^Matsuda, K.; Abe, Y; Fujioka, K (November 1957). "Kojibiose (2-O-alpha-D-Glucopyranosyl-D-Glucose): Isolation and Structure: Chemical Synthesis". Nature. 180 (4593): 985–6. Bibcode:1957Natur.180..985M. doi:10.1038/180985a0. PMID 13483573.
^T. Taga; Y. Miwa; Z. Min (1997). "α,β-Trehalose Monohydrate". Acta Crystallogr. C. 53 (2): 234–236. doi:10.1107/S0108270196012693.
disaccharide, disaccharide, also, called, double, sugar, biose, sugar, formed, when, monosaccharides, joined, glycosidic, linkage, like, monosaccharides, disaccharides, simple, sugars, soluble, water, three, common, examples, sucrose, lactose, maltose, sucrose. A disaccharide also called a double sugar or biose 1 is the sugar formed when two monosaccharides are joined by glycosidic linkage 2 Like monosaccharides disaccharides are simple sugars soluble in water Three common examples are sucrose lactose and maltose Sucrose a disaccharide formed from condensation of a molecule of glucose and a molecule of fructose Disaccharides are one of the four chemical groupings of carbohydrates monosaccharides disaccharides oligosaccharides and polysaccharides The most common types of disaccharides sucrose lactose and maltose have 12 carbon atoms with the general formula C12H22O11 The differences in these disaccharides are due to atomic arrangements within the molecule 3 The joining of monosaccharides into a double sugar happens by a condensation reaction which involves the elimination of a water molecule from the functional groups only Breaking apart a double sugar into its two monosaccharides is accomplished by hydrolysis with the help of a type of enzyme called a disaccharidase As building the larger sugar ejects a water molecule breaking it down consumes a water molecule These reactions are vital in metabolism Each disaccharide is broken down with the help of a corresponding disaccharidase sucrase lactase and maltase Contents 1 Classification 2 Formation 3 Properties 4 Assimilation 5 Common disaccharides 6 References 7 External linksClassification EditThere are two functionally different classes of disaccharides Reducing disaccharides in which one monosaccharide the reducing sugar of the pair still has a free hemiacetal unit that can perform as a reducing aldehyde group lactose maltose and cellobiose are examples of reducing disaccharides each with one hemiacetal unit the other occupied by the glycosidic bond which prevents it from acting as a reducing agent They can easily be detected by the Woehlk test or Fearon s test on methylamine 4 Non reducing disaccharides in which the component monosaccharides bond through an acetal linkage between their anomeric centers This results in neither monosaccharide being left with a hemiacetal unit that is free to act as a reducing agent Sucrose and trehalose are examples of non reducing disaccharides because their glycosidic bond is between their respective hemiacetal carbon atoms The reduced chemical reactivity of the non reducing sugars in comparison to reducing sugars may be an advantage where stability in storage is important 5 6 Formation EditThe formation of a disaccharide molecule from two monosaccharide molecules proceeds by displacing a hydroxy group from one molecule and a hydrogen nucleus a proton from the other so that the now vacant bonds on the monosaccharides join the two monomers together Because of the removal of the water molecule from the product the term of convenience for such a process is dehydration reaction also condensation reaction or dehydration synthesis For example milk sugar lactose is a disaccharide made by condensation of one molecule of each of the monosaccharides glucose and galactose whereas the disaccharide sucrose in sugar cane and sugar beet is a condensation product of glucose and fructose Maltose another common disaccharide is condensed from two glucose molecules 7 The dehydration reaction that bonds monosaccharides into disaccharides and also bonds monosaccharides into more complex polysaccharides forms what are called glycosidic bonds 8 Properties EditThe glycosidic bond can be formed between any hydroxy group on the component monosaccharide So even if both component sugars are the same e g glucose different bond combinations regiochemistry and stereochemistry alpha or beta result in disaccharides that are diastereoisomers with different chemical and physical properties Depending on the monosaccharide constituents disaccharides are sometimes crystalline sometimes water soluble and sometimes sweet tasting and sticky feeling Disaccharides can serve as functional groups by forming glycosidic bonds with other organic compounds forming glycosides Assimilation EditSee also Carbohydrate digestion Digestion of disaccharides involves breakdown into monosaccharides Common disaccharides EditDisaccharide Unit 1 Unit 2 BondSucrose table sugar cane sugar beet sugar or saccharose Glucose Fructose a 1 2 bLactose milk sugar Galactose Glucose b 1 4 Maltose malt sugar Glucose Glucose a 1 4 Trehalose Glucose Glucose a 1 1 aCellobiose Glucose Glucose b 1 4 Chitobiose Glucosamine Glucosamine b 1 4 Maltose cellobiose and chitobiose are hydrolysis products of the polysaccharides starch cellulose and chitin respectively Less common disaccharides include 9 Disaccharide Units BondKojibiose two glucose monomers a 1 2 10 Nigerose two glucose monomers a 1 3 Isomaltose two glucose monomers a 1 6 b b Trehalose two glucose monomers b 1 1 ba b Trehalose two glucose monomers a 1 1 b 11 Sophorose two glucose monomers b 1 2 Laminaribiose two glucose monomers b 1 3 Gentiobiose two glucose monomers b 1 6 Trehalulose a glucose monomer and a fructose monomer a 1 1 Turanose a glucose monomer and a fructose monomer a 1 3 Maltulose a glucose monomer and a fructose monomer a 1 4 Leucrose a glucose monomer and a fructose monomer a 1 5 Isomaltulose a glucose monomer and a fructose monomer a 1 6 Gentiobiulose a glucose monomer and a fructose monomer b 1 6 Mannobiose two mannose monomers either a 1 2 a 1 3 a 1 4 or a 1 6 Melibiose a galactose monomer and a glucose monomer a 1 6 Allolactose a galactose monomer and a glucose monomer b 1 6 Melibiulose a galactose monomer and a fructose monomer a 1 6 Lactulose a galactose monomer and a fructose monomer b 1 4 Rutinose a rhamnose monomer and a glucose monomer a 1 6 Rutinulose a rhamnose monomer and a fructose monomer b 1 6 Xylobiose two xylopyranose monomers b 1 4 References Edit Biose on www merriam webster org IUPAC Compendium of Chemical Terminology 2nd ed the Gold Book 1997 Online corrected version 2006 disaccharides doi 10 1351 goldbook D01776 Kwan Lam Peng 2000 Biology A course for O Level p 59 ISBN 9810190964 Ruppersberg Klaus Herzog Stefanie Kussler Manfred W Parchmann Ilka 2019 How to visualize the different lactose content of dairy products by Fearon s test and Woehlk test in classroom experiments and a new approach to the mechanisms and formulae of the mysterious red dyes Chemistry Teacher International doi 10 1515 cti 2019 0008 Nomenclature of Carbohydrates Recommendations 1996 2 Carb 36 Disaccharides Archived from the original on 2017 08 26 Retrieved 2010 07 21 Disaccharides and Oligosaccharides Retrieved 2008 01 29 Whitney Ellie Sharon Rady Rolfes 2011 Peggy Williams ed Understanding Nutrition Twelfth ed California Wadsworth Cengage Learning p 100 ISBN 978 0 538 73465 3 Glycosidic Link OChemPal Utah Valley University Retrieved 11 December 2013 F W Parrish W B Hahn G R Mandels July 1968 Crypticity of Myrothecium verrucaria Spores to Maltose and Induction of Transport by Maltulose a Common Maltose Contaminant J Bacteriol American Society for Microbiology 96 1 227 233 doi 10 1128 JB 96 1 227 233 1968 PMC 252277 PMID 5690932 Matsuda K Abe Y Fujioka K November 1957 Kojibiose 2 O alpha D Glucopyranosyl D Glucose Isolation and Structure Chemical Synthesis Nature 180 4593 985 6 Bibcode 1957Natur 180 985M doi 10 1038 180985a0 PMID 13483573 T Taga Y Miwa Z Min 1997 a b Trehalose Monohydrate Acta Crystallogr C 53 2 234 236 doi 10 1107 S0108270196012693 External links EditDisaccharides at the US National Library of Medicine Medical Subject Headings MeSH Retrieved from https en wikipedia org w index php title Disaccharide amp oldid 1127990369, wikipedia, wiki, book, books, library,
