Мальтаза: фермент расщепления мальтозы и крахмала

Enzyme

Maltase (, alpha glucosidase, glucoinvertase, glucosidosucrase, maltase glucoamylase, alpha glucopyranosidase, glucosidoinvertase, alpha D glucosidase, alpha glucoside hydrolase, alpha 1,4 glucosidase, alpha D glucoside glucohydrolase) is one type of alpha glucosidase enzymes located in the brush border of the small intestine. This enzyme catalyzes the hydrolysis of disaccharide maltose into two simple sugars of glucose. Maltase is found in plants, bacteria, yeast, humans, and other vertebrates. It is thought to be synthesized by cells of the mucous membrane lining the intestinal wall. Digestion of starch requires six intestinal enzymes. Two of these enzymes are luminal endo glucosidases named alpha amylases. The other four enzymes have been identified as different maltases, exo glucosidases bound to the luminal surface of enterocytes. Two of these maltase activities were associated with sucrase isomaltase (maltase Ib, maltase Ia). The other two maltases with no distinguishing characteristics were named maltase glucoamylase (maltases II and III). The activities of these four maltases are also described as alpha glucosidase because they all digest linear starch oligosaccharides to glucose.

Maltase is part of a group of intestinal enzymes called FamilyGH13 (Glycoside hydrolase family 13) that are responsible for breaking apart the α glucosidase linkages of complex carbohydrates into simple to use glucose molecules. The glucose molecules would then be used as a sort of "food" for cells to produce energy (Adenosine triphosphate) during Cellular respiration. The following are genes that can code for maltase:

Acid alpha glucosidase which is coded on the GAA gene is essential to breakdown complex sugars called Glycogen into glucose. Maltase glucoamylase which is coded on the MGAM gene plays a role in the digestion of starches. It is due to this enzyme in humans that starches of plant origin are able to digested. Sucrase isomaltase which is coded on the SI gene is essential for the digestion of carbohydrates including starch, sucrose and isomaltose. Alpha amylase 1 which is coded on the AMY1A gene is responsible of cleaving α glucosidase linkages in oligosaccharides and polysaccharides in order to produce starches and glycogen for the previous enzymes to catalyze. Higher quantities of this gene in the brain have been shown to lower the risk of Alzheimer's disease.

The mechanism of all FamilyGH13 enzymes is to break a α glucosidase linkage by hydrolyzing it. Maltase focuses on breaking apart maltose, a disaccharide that is a link between 2 units of glucose, at the α (1 >4) bond. The rate of hydrolysis is controlled by the size of the substrate (carbohydrate size).

The history of maltase discovery began when Napoleon Bonaparte declared a continental blockade in his “Berlin decree” in 1806. This initiated the search for alternative sources of sugar. In 1833 French chemists Anselm Payen and Jean Francois Persoz discovered a malt extract that converted starch into glucose which they called diastase at the time. In 1880, H. T. Brown discovered mucosal maltase activity and differentiated it from diastase, now called amylase. Fifty years later entering the genomic age, cloning and sequencing of the mucosal starch hydrolase confirmed Dahlqvist and Semenza's findings. AMD is a non sex linked autosomal recessive condition in which excessive accumulation of glycogen build up within lysosome vacuoles in nearly all types of cells all over the body. It is one of the more serious glycogen storage diseases affecting muscle tissue. AMD is categorized into three separate types based on the age of onset of symptoms in the affected individual. Infantile (Type a), childhood (Type b), and adulthood (Type c). The type of AMD is determined by the type of gene mutation localized on 17q23. Mutation type will determine production level of acid maltase. AMD is extremely fatal. Type a generally die of heart failure prior to age one. Type b die of respiratory failure between ages three to twenty four. Type c die of respiratory failure 10–20 years of the onset of symptoms.