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Lactose, or milk sugar, is a composed of and and has the molecular formula C12H22O11. Lactose makes up around 2–8% of (by mass). The name comes from (. ), the word for milk, plus the suffix used to name sugars. The compound is a white, , non- solid with a mildly sweet taste. It is used in the food industry.


Structure and reactions
Lactose is a composed of and , which form a β-1→4 linkage. Its is β-D-galactopyranosyl-(1→4)-D-glucose. The glucose can be in either the α- form or the β-pyranose form, whereas the galactose can have only the β-pyranose form: hence α-lactose and β-lactose refer to the form of the glucopyranose ring alone. Detection reactions for lactose are the Wöhlk- and Fearon's test. They can be used to detect the different lactose content of such as , lactose free milk, , , , , , etc.

Lactose is to glucose and galactose, in solution to , and to the corresponding polyhydric alcohol, . Lactulose is a commercial product, used for treatment of .


Occurrence and isolation
Lactose comprises about 2–8% of milk by weight. Several million tons are produced annually as a by-product of the .

or milk plasma is the liquid remaining after milk is curdled and strained, for example in the production of . Whey is made up of 6.5% solids, of which 4.8% is lactose, which is purified by crystallisation. Industrially, lactose is produced from whey permeate – whey filtrated for all major . The protein fraction is used in and while the permeate can be evaporated to 60–65% solids and crystallized while cooling., DOI is open access Lactose can also be isolated by dilution of whey with .


Metabolism
Infant nurse on their mothers to drink milk, which is rich in lactose. The intestinal villi secrete the (β-D-galactosidase) to digest it. This enzyme cleaves the lactose molecule into its two subunits, the simple glucose and galactose, which can be absorbed. Since lactose occurs mostly in milk, in most mammals, the production of lactase gradually decreases with maturity due to weaning; the removal of lactose from the diet removes the metabolic pressure to continue to produce lactase for its digestion.

Many people with ancestry in , , , the belt in , and a few other parts of maintain lactase production into adulthood due to selection for genes that continue lactase production. In many of these areas, milk from mammals such as , , and is used as a large source of food. It was in these regions that genes for lifelong lactase production first . The genes of adult lactose tolerance have evolved independently in various ethnic groups.. By descent, more than 70% of western Europeans can digest lactose as adults, compared with less than 30% of people from areas of Africa, eastern and south-eastern Asia and Oceania.. In people who are lactose intolerant, lactose is not broken down and provides food for gas-producing , which can lead to diarrhea, bloating, flatulence, and other gastrointestinal symptoms.


Biological properties
The of lactose is 0.2 to 0.4, relative to 1.0 for . For comparison, the sweetness of glucose is 0.6 to 0.7, of is 1.3, of galactose is 0.5 to 0.7, of is 0.4 to 0.5, of is 0.4, and of is 0.6 to 0.7.

When lactose is completely digested in the , its is 4 kcal/g, or the same as that of other . However, lactose is not always fully digested in the small intestine. Depending on ingested dose, combination with meals (either solid or liquid), and lactase activity in the , the caloric value of lactose ranges from 2 to 4 kcal/g. Undigested lactose acts as . It also has positive effects on absorption of , such as and .

The of lactose is 46 to 65. For comparison, the glycemic index of glucose is 100 to 138, of sucrose is 68 to 92, of maltose is 105, and of fructose is 19 to 27.

Lactose has relatively low among sugars.

(2006). 9781420004311, CRC Press. .
This is because it is not a substrate for formation and it is not rapidly by . The buffering capacity of milk also reduces the cariogenicity of lactose.


Applications
Its mild flavor and easy handling properties have led to its use as a carrier and stabiliser of aromas and pharmaceutical products. Lactose is not commonly added directly to food, because its low solubility can lead to a gritty mouthfeel. is a notable exception, where lactose is added to match the composition of human milk. However, lactose-reduced formulas are increasing in popularity.

One of the undesirable properties of lactose utilization is its low solubility, which can result in crystallization, giving a gritty and sandy mouthfeel in the final product. Usually, in supersaturated solution, sugars tend to crystallize, also forming big agglomerates, depending on the process condition.

Lactose is not fermented by most during brewing, which may be used to advantage. For example, lactose may be used to sweeten stout beer; the resulting beer is usually called a or a cream stout.

Yeast belonging to the genus have a unique industrial application, as they are capable of fermenting lactose for ethanol production. Surplus lactose from the whey by-product of dairy operations is a potential source of alternative energy..

Another significant lactose use is in the pharmaceutical industry. Lactose is added to tablet and capsule drug products as an ingredient because of its physical and functional properties (examples are , or among many others). For similar reasons, it can be used to dilute illicit drugs such as cocaine or heroin.


History
The first crude isolation of lactose, by Italian physician Fabrizio Bartoletti (1576–1630), was published in 1633.Fabrizio Bartoletti, Methodus in dyspnoeam ... Procedure, (Bologna ("Bononia"), (Italy): Nicolò Tebaldini for the heirs of Evangelista Dozza, 1633), p. 400. From page 400: "italic=no seri hæc. Destilla leni balnei calore serum lactis, donec in fundo vasis butyracea fœx subsideat, cui hærebit salina quædam substantia subalbida. Hanc curiose segrega, est enim sal seri essentiale; seu nitrum, cujus causa nitrosum dicitut serum, huicque tota abstergedi vis inest. Solve in aqua propria, & coagula. Opus repete, donec seri cremorem habeas sapore omnino mannam referentem." (This is the manna of whey. Note: Gently distill whey via a heat bath until the buttery scum settles to the bottom of the vessel, to which substance some whitish salt i.e., attaches. This curious substance separated, is truly the essential salt of whey; or, on account of which nitre, is called "nitre of whey", and all life force is in this that will be expelled. Note: Dissolve it in its own water and coagulate. Repeat the operation until you have cream of whey, recalling, by its taste, only manna.)
In 1688, the German physician Michael Ettmüller (1644–1683) reprinted Bartoletti's preparation. See: Ettmüller, Michael, Opera Omnia ... (Frankfurt am Main ("Francofurtum ad Moenum"), Germany: Johann David Zunner, 1688), book 2, page 163. From page 163: "Undd Bertholetus praeparat ex sero lactis remedium, quod vocat mannam S. alchemical seri lactis vid. in Encyclopaed . p. 400. Praeparatio est haec: ... " (Whence Bartoletti prepared from milk whey a medicine, which he called manna or salt of milk whey; see in his Encyclopedia note:, p. 400. This is the preparation: ... )
In 1700, the Venetian pharmacist Lodovico Testi (1640–1707) published a booklet of testimonials to the power of milk sugar ( saccharum lactis) to relieve, among other ailments, the symptoms of arthritis.Lodovico Testi, De novo Saccharo Lactis On (Venice, (Italy): Hertz, 1700). In 1715, Testi's procedure for making milk sugar was published by Antonio Vallisneri.Ludovico Testi (1715) "Saccharum lactis" (Milk sugar), Academiae Caesareo-Leopoldinae naturae curiosorum ephemerides, ... , 3 : 69–79. The procedure was also published in Giornale de' letterati d'Italia in 1715. Lactose was identified as a sugar in 1780 by Carl Wilhelm Scheele.See:
  • Carl Wilhelm Scheele (1780) "Om Mjölk och dess syra" (About milk and its acid), Kongliga Vetenskaps Academiens Nya Handlingar (New Proceedings of the Royal Academy of Science), 1 : 116–124. From page 116: "Det år bekant, at Ko-mjölk innehåller Smör, Ost, Mjölk-såcker, ... " (It is known, that cow's milk contains butter, cheese, milk-sugar, ... )
  • Carl Wilhelm Scheele (1780) "Om Mjölk-Såcker-Syra" (On milk-sugar acid), Kongliga Vetenskaps Academiens Nya Handlingar (New Proceedings of the Royal Academy of Science), 1 : 269–275. From pages 269–270: "Mjölk-Såcker år et sal essentiale, som uti Mjölken finnes uplöst, och som, för dess sötaktiga smak skull, fått namn af såcker." (Milk sugar is an essential salt, which is found dissolved in milk, and which, on account of its sweet taste, has the name of "sugar".)

In 1812, Heinrich Vogel (1778–1867) recognized that glucose was a product of hydrolyzing lactose.See:

Fischer established the configuration of galactose in:
  • Emil Fischer and Robert S. Morrell (1894) "Ueber die Configuration der Rhamnose und Galactose" (On the configuration of rhamnose and galactose), Berichte der Deutschen chemischen Gesellschaft zu Berlin, 27 : 382–394. The configuration of galactose appears on page 385.

Lactose was named by the French chemist Jean Baptiste André Dumas (1800–1884) in 1843.Dumas, Traité de Chimie, Appliquée aux Arts, volume 6 (Paris, France: Bechet Jeune, 1843), p. 293. In 1856, Pasteur named galactose "lactose".Pasteur (1856) "Note sur le sucre de lait" (Note on milk sugar), Comptes rendus, 42 : 347–351. From page 348: "Je propose de le nommer lactose ." (I propose to name it lactose.) In 1860, Marcellin Berthelot renamed it "galactose", and transferred the name "lactose" to what is now called lactose.Marcellin Berthelot, Chimie organique fondée sur la synthèse Organic (Paris, France: Mallet-Bachelier, 1860), vol. 2, pp. 248–249 and pp. 268–270. It has a formula of C12H22O11 and the hydrate formula C12H22O11·H2O, making it an of sucrose.


See also


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