Any of a class of sugars, including lactose and sucrose, that are composed of two monosaccharides.
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di·sac·cha·ride (dī-săk'ə-rīd') ![]() |
Any of a class of sugars, including lactose and sucrose, that are composed of two monosaccharides.
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| Chemistry Dictionary: disaccharide |
A sugar consisting of two linked monosaccharide molecules. For example, sucrose comprises one glucose molecule and one fructose molecule bonded together.
| Food and Nutrition: disaccharide |
Sugars composed of two monosaccharide units; the nutritionally important disaccharides are sucrose, lactose, and maltose. See carbohydrate.
| Food and Fitness: disaccharide |
A carbohydrate resulting from the combination of two monosaccharides (single sugars). For example, when glucose and fructose combine, they form the disaccharide sucrose; glucose and galactose form lactose; and two glucose molecules form maltose. During digestion, disaccharides are broken down into monosaccharides which are absorbed into the bloodstream and carried to the liver for processing, after which their main use is as a source of energy.
| Dental Dictionary: disaccharide |
A general term for simple carbohydrates (sugars) formed by the union of two monosaccharide molecules. Sucrose is the most common disaccharide sugar.
| Sports Science and Medicine: disaccharide |
A sugar formed when two monosaccharides join together by a reaction in which water is removed (condensation). For example, glucose and fructose combine to form sucrose. Other common disaccharides are lactose (formed from glucose and galactose) and maltose (formed from two molecules of glucose).
| Veterinary Dictionary: disaccharide |
Any of a class of sugars each molecule of which yields two molecules of monosaccharide on hydrolysis.
| Wikipedia: Disaccharide |
A disaccharide is the carbohydrate formed when two monosaccharides undergo a condensation reaction which involves the elimination of a small molecule, such as water, from the functional groups only. Like monosaccharides, disaccharides also dissolve in water, taste sweet and are called sugars.[1]
'Disaccharide' is one of the four chemical groupings of carbohydrates (monosaccharide, disaccharide, oligosaccharide, and polysaccharide).
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There are two basic types of disaccharides: reducing disaccharides, in which the monosaccharide components are bonded by hydroxyl groups; and non-reducing disaccharides, in which the components bond through their anometric centers.[2]
It is formed when two monosaccharides are joined together and a molecule of water is removed. For example; milk sugar (lactose) is made from glucose and galactose whereas cane sugar (sucrose) is made from glucose and fructose.
The two monosaccharides are bonded via a dehydration reaction (also called a condensation reaction or dehydration synthesis) that leads to the loss of a molecule of water and formation of a glycosidic bond.
The glycosidic bond can be formed between any hydroxyl 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.
| Disaccharide | Unit 1 | Unit 2 | Bond |
| Sucrose (table sugar, cane sugar, saccharose, or beet sugar) | glucose | fructose | α(1→2) |
| Lactulose | galactose | fructose | β(1→4) |
| Lactose (milk sugar) | galactose | glucose | β(1→4) |
| Maltose | glucose | glucose | α(1→4) |
| Trehalose | glucose | glucose | α(1→1)α |
| Cellobiose | glucose | glucose | β(1→4) |
Maltose and cellobiose are hydrolysis products of the polysaccharides, starch and cellulose, respectively.
Less common disaccharides include[3]:
| Disaccharide | Units | Bond |
| Kojibiose | two glucose monomers | α(1→2) [4] |
| Nigerose | two glucose monomers | α(1→3) |
| Isomaltose | two glucose monomers | α(1→6) |
| β,β-Trehalose | two glucose monomers | β(1→1) |
| Sophorose | two glucose monomers | β(1→2) |
| Laminaribiose | two glucose monomers | β(1→3) |
| Gentiobiose | two glucose monomers | β(1→6) |
| Turanose | a glucose monomer and a fructose monomer | α(1→3) |
| Maltulose | a glucose monomer and a fructose monomer | α(1→4) |
| Palatinose | a glucose monomer and a fructose monomer | α(1→6) |
| Gentiobiulose | a glucose monomer and a fructose monomer | β(1→6) |
| Mannobiose | two mannose monomers | either α(1→2), α(1→3), α(1→4), or α(1→6) |
| Melibiose | a galactose monomer and a glucose monomer | α(1→6) |
| Melibiulose | a galactose monomer and a fructose monomer | α(1→6) |
| Rutinose | a rhamnose monomer and a glucose monomer | α(1→6) |
| Rutinulose | a rhamnose monomer and a fructose monomer | β(1→6) |
| Xylobiose | two xylopyranose monomers | β(1→4) |
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| melibiose | |
| palatinose | |
| N-acetylgalactosamine |
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