Search results
Results from the WOW.Com Content Network
Galactose (/ ɡ ə ˈ l æ k t oʊ s /, galacto-+ -ose, "milk sugar"), sometimes abbreviated Gal, is a monosaccharide sugar that is about as sweet as glucose, and about 65% as sweet as sucrose. [3] It is an aldohexose and a C-4 epimer of glucose. [4] A galactose molecule linked with a glucose molecule forms a lactose molecule.
The molecular structure of α-lactose, as determined by X-ray crystallography. Lactose crystals, viewed under polarized light. Lactose is a disaccharide composed of galactose and glucose, which form a β-1→4 glycosidic linkage. Its systematic name is β-D-galactopyranosyl-(1→4)-D-glucose.
l-Glucose is an organic compound with formula C 6 H 12 O 6 or O=CH[CH(OH)] 5 H, specifically one of the aldohexose monosaccharides. As the l-isomer of glucose, it is the enantiomer of the more common d-glucose. l-Glucose does not occur naturally in living organisms, but can be synthesized in the laboratory.
Oligosaccharides of glucose combined with other sugars serve as important energy stores. These include lactose, the predominant sugar in milk, which is a glucose-galactose disaccharide, and sucrose, another disaccharide which is composed of glucose and fructose. Glucose is also added onto certain proteins and lipids in a process called ...
For instance, galactose and glucose are both aldohexoses, but have different physical structures and chemical properties. The monosaccharide glucose plays a pivotal role in metabolism , where the chemical energy is extracted through glycolysis and the citric acid cycle to provide energy to living organisms.
It is used as a high-fructose syrup, which is manufactured from hydrolyzed corn starch that has been processed to yield corn syrup, with enzymes then added to convert part of the glucose into fructose. [74] Galactose generally does not occur in the free state but is a constituent with glucose of the disaccharide lactose or milk sugar. It is ...
Structure of ceramide, galactosylceramide and glucosylceramide. Galactose or glucose sugars can be attached to a hydroxyl group of ceramide lipids in a different form of O-glycosylation, as it does not occur on proteins. [6] This forms glycosphingolipids, which are important for the localisation of receptors in membranes. [8]
A galactoside is a glycoside containing galactose. The H of the OH group on carbon-1 of galactose is replaced by an organic moiety. [1] Structure of ONPG, an example of a β-galactoside. Depending on whether the glycosidic bond lies "above" or "below" the plane of the galactose molecule, galactosides are classified as α-galactosides or β ...