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・ Glycogen phosphorylase isoenzyme BB
・ Glycogen storage disease
・ Glycogen storage disease type 0
・ Glycogen storage disease type I
・ Glycogen storage disease type II
・ Glycogen storage disease type III
・ Glycogen storage disease type IV
・ Glycogen storage disease type IX
・ Glycogen storage disease type V
・ Glycogen storage disease type VI
・ Glycogen storage disease type XI
・ Glycogen synthase
・ Glycogen synthase kinase
・ Glycogen-branching enzyme deficiency
・ Glycogenase
Glycogenesis
・ Glycogenic acanthosis
・ Glycogenin
・ Glycogenin-1
・ Glycogenolysis
・ Glycoinformatics
・ Glycol cleavage
・ Glycol dehydration
・ Glycol distearate
・ Glycol ethers
・ Glycol nucleic acid
・ Glycol stearate
・ Glycolaldehyde
・ Glycolaldehyde dehydrogenase
・ Glycolate dehydrogenase


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Glycogenesis : ウィキペディア英語版
Glycogenesis

Glycogenesis is the process of glycogen synthesis, in which glucose molecules are added to chains of glycogen for storage. This process is activated during rest periods following the Cori cycle, in the liver, and also activated by insulin in response to high glucose levels, for example after a carbohydrate-containing meal.
==Steps==
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* Glucose is converted into glucose-6-phosphate by the action of glucokinase or hexokinase.
* Glucose-6-phosphate is converted into glucose-1-phosphate by the action of phosphoglucomutase, passing through the obligatory intermediate glucose-1,6-bisphosphate.
* Glucose-1-phosphate is converted into UDP-glucose by the action of the enzyme UDP-glucose phosphorylase. Pyrophosphate is formed, which is later hydrolysed by pyrophosphatase into two phosphate molecules.
* Glycogenin, a homodimer, has a tyrosine residue on each subunit that serves as the anchor for the reducing end of glycogen. Initially, about eight UDP-glucose molecules are added to each tyrosine residue by glycogenin, forming α(1→4) bonds.
* Once a chain of eight glucose monomers is formed, glycogen synthase binds to the growing glycogen chain and adds UDP-glucose to the 4-hydroxyl group of the glucosyl residue on the non-reducing end of the glycogen chain, forming more α(1→4) bonds in the process.
* Branches are made by glycogen branching enzyme (also known as amylo-α(1:4)→α(1:6)transglycosylase), which transfers the end of the chain onto an earlier part via α-1:6 glycosidic bond, forming branches, which further grow by addition of more α-1:4 glycosidic units.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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