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Enzymatic of dietary in gastro- intestinal-tract.

Amino

Amino : 1. There are 20 different , they are monomeric constituents of proteins 2. They act as precursors of other containing biologically important compounds, like , etc. 3. Can be used as source.

We will be discussing just the catabolism of the amino acids ( AAs), to generate energy. There are three major steps in catabolism of AAs. 1. Removal of amino group: by I. : Transfer of amino gp to a-ketoglutarate yielding glutamate II. : removal of amino gp from glutamate to release III. Other deamination processes.

2. Cycle: Conversion of NH 3 to urea for excretion

3. Metabolic break down of skeleton to generate common

intermediates that can be catabolized to CO 2 or used in anabolic pathways to be stored as or .

Transamination: Transfer of amino group to a-ketoglutarate. There are several Excretory forms of Nitrogen aminotransferases specific to different amino acids. In this step amino group from all the amino acids are transferred to a-ketoglutarate and they exist as glutamate. or aminotransferases require pyridoxal-5’-phophate PLP (vitamine B6 derivative) PLP is very important for many enzymatic reactions.

1 -bound (d) and amino acid-bound PLP In 3D structural model

Pyridoxal as carrier of amino group (a) and it’s enzyme-bound form (b) through Schiff’s base

Oxidative deamination: In the amino gp of glutamate is released Transport of excess as amonia, regenerating generating a-ketoglutarate, by an enzyme glutamate ammonia by : dehydrogenase. Excess ammonia is toxic to animal tissues. Other than amino acid requires NAD+ or NADP+ as cofactor. This is the catabolism in tissues ammonia is also only enzyme known that has specificity for both type of cofactor. produced as a result of This enzyme is allosterically inhibited by GTP and activated by ADP. degradation. Glutamine synthase catalyses the synthesis of glutamine by adding the ammonia to glutamate at the expense of ATP . Glutamine is a non-toxic carrier of ammonia. It is transported to liver or via . In liver or kidney mitochondria, the glutamine is converted to glutamate and ammonia. Ammonia is incorporated in in liver to be excreted.

Glucose- cycle: Amino group from excess glutamate produced in muscle as a result of amino acid catabolism, synthase-I Reaction: is transferred to pyruvate Ammonia released from the resulting in the formation of oxidative deamination is alanine. incorporated in carbamoyl Alanine is another safe way to phosphate by using ATP and transport ammonia from muscle to bicarbonate. liver via blood. In liver alanine aminotransferase transfers the amino gp to glutarate N-acetyl glutamine is a positive and pyruvate regenerated is used regulator of this enzyme. in . Carbamoyl phosphate enters Glucose produced by the urea cycle in the gluconeogenesis is transported to muscle where it enters the mitochondria. . Thus the excess puruvate and ammonia generated in muscle are safely transported to liver.

2 Possible therapies for the patients with defect in urea cycle: Interaction of Urea Cycle and Cycle via Aspartate- Argininosuccinate shunt 1. Defined containing just the minimum amount of essential amino acids. 2. Feeding the patients with Benzoate or phenylacectate: These compound react with and glutamine respectively forming non-toxic compounds that are excreted in . Thus the body runs low in glycine and glutamine and starts synthasizing these AA using the ammonia available in system. Thus clearing the system of excess ammonia.

3. In the patients with N-acetylglutamate synthase deficiency, Carbamoyl glutamate can act as activator of carbamoyl phosphate synthase.

3 Entry of the carbon skeleton of AAs in Regulation of urea cycle: 1. involved in urea cycle are synthesized at higher level when proteins are utilized for energy production (starvation, or availability of fat and -free diet. 2. The carbamoyl phosphate synthase is allosterically activated by N-acetylglutamate .

Some of the cofactors involved in amino acid

4 Catabolic pathway of Glycine, , , ,alanine and Metabolic fates of Glycine

Catabolic pathways for Arg, His, Pro, Glu, Gln Catabolic pathways of and

Catabolic pathway of Tryptophan, , phenyl alanine, and Tryptophan as a precursor of other important compound lucine

5 Catabolism of and tyrosine Role of tetrahydrobiopterine in phenylalanine hydroxylase reaction

Alternative pathways for the Met, Ile, Thr, catabolism of phenylalanine in Val patients with catabolism The end product phenylpyruvate accumulates in liver, blood and urine. Phenylacetate and phenylactate are also found in urine.

Catabolic pathways of three branched chain amino acids

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