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Alpha keto acids can than be converted to glucose to maintain proper blood sugar levels.
It is classified as a keto acid.
The alpha keto acids are then converted by the liver to glucose in a process called gluconeogenesis.
Amino acids are released into the blood and converted in the liver to alpha keto acids.
Common types of keto acids include:
The other product of transamidation is a keto acid that enters the citric acid cycle.
The amino group is fed into the urea cycle, leaving a deaminated carbon skeleton in the form of a keto acid.
These opines are condensation products of amino acids and keto acids or may be derived from sugars.
Alpha-ketoglutarate, (also known as 2-oxo glutarate) is a 5-carbon keto acid derived from glutamic acid.
It is the keto acid produced by deamination of glutamate, and is an intermediate in the Krebs cycle.
Transamination is demonstrated if the corresponding new amino acid and keto acid are formed, as revealed by paper chromatography.
Keto acids (or oxoacids) are organic compounds that contain a carboxylic acid group and a ketone group.
Ketogenic amino acids can be deaminated to produce alpha keto acids and ketone bodies.
Alpha keto acids are used primarily as energy for liver cells and in fatty acid synthesis, also in the liver.
Unlike related keto acids, it is not an intermediate or metabolite associated with amino acids and its origin is unknown.
The vast majority are secondary amine derivatives formed by condensation of an amino acid, either with a keto acid or a sugar.
Several of these keto acids are intermediates in the citric acid cycle, for example the deamination of glutamate forms α-ketoglutarate.
In this situation, proteins are converted to amino acids which are then converted in the liver to alpha keto acids.
In the formation of simple β-carboline alkaloids, such as harmine and harmaline, pyruvic acid acts as the keto acid.
They catabolize a variety of energy sources including carbohydrates, glycerol, lactate,malate, citrate, arginine, agmatine, and many keto acids .
Oxaloacetate is one of the keto acids preferred by transaminases, and so will be recycled to aspartate, maintaining the flow of nitrogen into the urea cycle.
In ketoacidosis, the body fails to adequately regulate ketone production causing such a severe accumulation of keto acids that the pH of the blood is substantially decreased.
Effect of lipoic acid in patient with defective activity of pyruvate dehydrogenase, 2-oxoglutarate dehydrogenase, and branched-chain keto acid dehydrogenase.
Branched-chain keto acid dehydrogenase is a multienzyme complex associated with the inner membrane of mitochondria, and functions in the catabolism of branched-chain amino acids.
BCKDHB: branched chain keto acid dehydrogenase E1, beta polypeptide (maple syrup urine disease)