galactokinase
The enzyme that synthesizes starch from glucose-1-phosphate is starch synthase. This enzyme catalyzes the condensation reaction of glucose molecules to form the starch polymer.
The conversion of glyceraldehyde 3 phosphate to 1, 3 bisphosphoglycerate catalyzed byglyceraldehyde 3 phosphate dehydrogenase using NAD+ and Pi
The enzyme creatine kinase catalyzes the reaction that creates creatine phosphate. This reaction involves transferring a phosphate group from ATP to creatine, forming creatine phosphate and ADP. Creatine phosphate serves as a short-term energy reservoir in muscle cells.
G6PD deficiency is caused by one copy of a defective G6PD gene in males or two copies of a defective G6PD gene in females. Hemolytic anemic attacks can be caused by oxidants, infection, and or by eating fava beans.
The breakdown of creatine phosphate is regulated by the enzyme creatine kinase. This enzyme catalyzes the transfer of a phosphate group from creatine phosphate to ADP, forming ATP. The reaction is reversible, and the activity of creatine kinase helps to maintain energy balance in cells.
glucose and galactose http://users.rcn.com/jkimball.ma.ultranet/BiologyPages/C/Carbohydrates.html
The enzyme that synthesizes starch from glucose-1-phosphate is starch synthase. This enzyme catalyzes the condensation reaction of glucose molecules to form the starch polymer.
Glucose is the substrate that is converted into glucose 6-phosphate by the enzyme hexokinase. Hexokinase catalyzes the phosphorylation of glucose to glucose 6-phosphate in the first step of glycolysis.
The lack of the enzyme galactose-1-phosphate uridyltransferase (GALT) causes galactosemia. This enzyme is responsible for the breakdown of galactose in the body, and its deficiency leads to the accumulation of galactose and its toxic byproducts.
The enzyme that converts lactose to glucose and galactose is lactase. Lactase is located in the brush border of the small intestine where it breaks down lactose into its two component sugars, glucose and galactose, which can then be absorbed into the bloodstream.
Hexokinase
Galactosemia is primarily caused by mutations in the GALT gene, which encodes an enzyme called galactose-1-phosphate uridylyltransferase. Mutations in this gene result in reduced or absent enzyme activity, leading to the accumulation of galactose-1-phosphate in the body.
Lactose is composed of one glucose molecule and one galactose molecule bonded together. Upon digestion by the enzyme lactase, lactose is broken down into its individual glucose and galactose molecules for absorption in the body.
The combination of glucose and galactose forms lactose, which is a disaccharide commonly found in milk. Lactose is broken down by the enzyme lactase into its constituent monosaccharides during digestion.
Lactose is a disaccharide composed of glucose and galactose. Upon hydrolysis, lactose breaks down into its component monosaccharides, glucose, and galactose. This process is catalyzed by the enzyme lactase.
Lactose intolerance is the inability to efficiently convert lactose into glucose and galactose, a reaction catalyzed by the enzyme lactase. (A rule of thumb for enzyme nomenclature is that many enzyme names typically take most of the name of their substrate and slap an "-ase" at the end.)
Galactose is obtained from lactose (the milk sugar) after its hydrolysis carried out by the enzyme beta-galactosidase (or lactase) yielding beta-D-glucose and alpha-D-galactose.