Galactose Structure Overview
Lactose is created when a galactose molecule binds to a glucose molecule. Its molecular weight is 180 g/mol. Lactose, which is present in milk and dairy products, is its primary dietary source. A few fruits and vegetables contain galactose in addition to lactose. Galactosemia is a deadly condition that may be easily detected at birth but is not treatable due to recessive genetics.
What is Galactose?
The monosaccharide sugar galactose, frequently abbreviated as Gal, is about 65% as sweet as sucrose and about as sweet as glucose. It is a C-4 epimer of glucose and an aldohexose. A lactose molecule is created when two molecules of galactose and glucose are joined. Galactan, a naturally occurring type of polymeric carbohydrate, is a polymeric form of galactose that may be found in hemicellulose and serves as the core of Galatians. Because it is a part of the glycoproteins (oligosaccharide-protein complexes) that are present in nerve tissue, D-galactose is sometimes referred to as brain sugar.
Etymology of Galactose Structure
The Greek letter o, galactose, which means "of milk," and the general chemical suffix for sugars, -ose, are the sources of the term galactose, which was first used by Charles Weissman in the middle of the 19th century. The word's origin is similar to that of lactose in that both words derive from roots that mean "milk sugar." A disaccharide comprising galactose and glucose is lactose.
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Formula for Galactose Structure
A monosaccharide sugar, galactose has a molecular mass of 180 g/mol and the chemical formula is C₆H₁₂O₆. Galactose and glucose combine to generate the disaccharide known as lactose. Both cyclic and open-chain cyclic forms of galactose are present, with the latter having a carbonyl group connected to the chain's terminus.
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What is the Structure of Galactose?
Open-chain and cyclic galactose structures are two types of galactose structures. The open-chain form has a carbonyl at the end. The galactose formula can be used to help build its structure.Two of the isomers have pyranose rings with six members, whereas the other two have furanose rings with five members. The exocyclic 1,2-diol of galactofuranose, which is present in bacteria, fungi, and protozoa, is identified by the putative chordate immune lectin intelectin. The cyclic form has two anomers,alpha, and beta because the change from the open-chain to the cyclic form necessitates the development of a new stereocenter at the location of the open-chain carbonyl. In the beta form, the alcohol group is in the equatorial position, whereas in the alpha form, it is in the axial position.
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Properties of Galactose Structure
The following table gives details about the properties of galactose structure-
Particulars | Details |
IUPAC Name | (3R,4S,5R,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol |
Chemical Formula of Galactose Structure | C₆H₁₂O₆ |
Molecular Mass of Galactose Structure | 180.156 g/mol |
Odour | Odourless |
Density of Galactose Structure | 1.5 g/cm⁻³ |
Appearance | White Solid |
Melting Point of Galactose Structure | 168–170 ℃ |
Hydrogen Bond Donor Count | 5 |
Hydrogen Bond Acceptor Count | 6 |
Rotatable Bond Count | 1 |
Solubility | Soluble in water but slightly soluble in ethanol |
Facts about Galactose Structure
A simple sugar called galactose is metabolized into energy by the liver. This sugar is frequently consumed by people and has a number of uses. Since galactose is a precursor to the creation of glucose, it is crucial for the generation of energy. The body's demand for galactose is satisfied through the metabolic conversion of D-glucose to D-galactose. It is an essential part of the glycolipids found in the myelin sheaths of nerve cells in the brain. It is hence also referred to as "brain sugar."
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Uses of Galactose Structure
The following are some of the applications of galactose structure-
- A kind of sugar called galactose is essential for the body's metabolism and the supply of energy.
- Galactose is a tool used by researchers to explore certain disorders.
- It is crucial during the formative stages of human development.
- Some common vaccinations and over-the-counter medicines have galactose as a component.
- Studying the management and detection of conditions including Hepatitis C, liver cancer, Wilson's disease, diabetic macular edema, and focal segmental glomerulosclerosis is beneficial.
- The human body uses it as a route to produce glucose as fuel.
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Sources of Galactose Structure
Our diet's main source of galactose is lactose, which may be found in dairy products like yogurt and milk. These sources break down into glucose and galactose after digestion. Celery, cherries, honey, hamburgers with toppings, low-fat mozzarella, plums, avocados, sweetened yogurt, milk-based puddings, and kiwifruit are a few examples of foods high in galactose.
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Health Risks of Galatose Structure
The following are the health hazards of galactose structure-
- Galactose consumption too much might cause tooth decay.
- It might have minor laxative effects when taken in large doses.
- Some individuals may even experience negative side effects, including rashes, itching, extreme vertigo, and respiratory problems.
Galactosemia
Galactosemia is a genetic condition in which a person's body no longer has the capacity to convert galactose to glucose. As a result, the person has difficulty with carbohydrate metabolism and cannot properly digest milk and dairy products. The Galactose-1-phosphate uridinetransferase (GALT) enzyme, which is crucial for converting galactose into glucose, becomes inadequate in the body as a result of this illness. Treatment should begin as soon as possible after birth because the problem is genetically transmitted, and failing to do so might result in both intellectual handicaps and life-threatening conditions.