L12 Amino acid metabolism Flashcards

1
Q

Are excess amino acids stored?

A

No, which is the key difference betwen amino acids and other 2 types of oxidizable biomolecules (i.e. carbohydrates and fatty acids)

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2
Q

What is the universal amino group acceptor?

A

alpha-Ketoglutarate;
alpha-Ketoglutarate is one of the intermediate metabolite formed in TCA

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3
Q

What is the first step in the catabolism of most amino acids?

A

Transamination in cytosol of the liver cells

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4
Q

What are the main steps of amino acids catabolism?

A

(1) Transamination in cytosol of the liver cells
(alpha-Ketoglutarate to glutamate)
(2) Oxidative deamination of glutamate in mitochondrial matrix of liver cells
(glutamate back to alpha-Ketoglutarate)

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5
Q

Where is urea formed?

A

In liver

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6
Q

In non-hepatic tissues, ammonia is converted to which metabolite?

A

Glutamine

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7
Q

Give me the chemical form of amide group, amino group, and ammonia

A

amide group: -NH2
amino group: -NH3+
ammonia: NH4+

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8
Q

To remove ammonia as urea in liver, what is the first step?

A

Condensation of ammonia with CO2

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9
Q

Where does condensation of ammonia with CO2 takes place?

A

Mitochondrial matrix

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10
Q

What are the 4 enzymes involved in the Urea cycle?

A

(1) Ornithine transcarbamoylase
(2) Argininosuccinate synthetase
(3) Argininosucciante lyase
(4) Arginase

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11
Q

Phenylketonuria is a disease due to defective of which enzyme?

A

Defective phenylalanine hydroxylase

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12
Q

Give me the chemical form of Nitrate and Nitrite

A

Nitrate: NO3-
Nitrite: NO2-

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