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disaccharide

 
Dictionary: di·sac·cha·ride   (dī-săk'ə-rīd') pronunciation
n.
Any of a class of sugars, including lactose and sucrose, that are composed of two monosaccharides.


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Chemistry Dictionary: disaccharide
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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
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Sugars composed of two monosaccharide units; the nutritionally important disaccharides are sucrose, lactose, and maltose. See carbohydrate.

Food and Fitness: disaccharide
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double sugar

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
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n

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
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double sugar

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
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Any of a class of sugars each molecule of which yields two molecules of monosaccharide on hydrolysis.

Wikipedia: Disaccharide
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Sucrose, a common 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).

Contents

Classification

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]

Formation

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.

Properties

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.

Common disaccharides

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)

References

  1. ^ International Union of Pure and Applied Chemistry. "disaccharides". Compendium of Chemical Terminology Internet edition.
  2. ^ "Disaccharides and Oligiosaccharides". http://faculty.virginia.edu/mcgarveylab/Carbsyn/Carblist/html/disacch.html. Retrieved 2008-01-29. 
  3. ^ F.W.Parrish; W.B.Hahn,G.R.Mandels} (July 1968). "[http://jb.asm.org/cgi/reprint/96/1/227.pdf 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. http://jb.asm.org/cgi/reprint/96/1/227.pdf. Retrieved 2008-11-21. 
  4. ^ Matsuda, K. (November 1957). "Kojibiose (2-O-alpha-D-Glucopyranosyl-D-Glucose): Isolation and Structure: Chemical Synthesis". Nature 180: 985. doi:10.1038/180985a0. 

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Dictionary. The American Heritage® Dictionary of the English Language, Fourth Edition Copyright © 2007, 2000 by Houghton Mifflin Company. Updated in 2009. Published by Houghton Mifflin Company. All rights reserved.  Read more
Chemistry Dictionary. A Dictionary of Chemistry. Sixth Edition. Copyright © Market House Books Ltd, 2008. All rights reserved.  Read more
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Food and Fitness. Food and Fitness: A Dictionary of Diet and Exercise. Copyright © 1997, 2003 by Oxford University Press. All rights reserved.  Read more
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