Amino acid catabolism Flashcards

1
Q

What is catabolism?

A

the breakdown of complex molecules in living organisms to form simpler ones, together with the release of energy

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2
Q

can amino acids be stored if not needed?

A

No, they are degraded

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3
Q

Where does amino acid degradation happen?

A

In the liver

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4
Q

Where do most of the amino acids come from?

A

From the diet - absorption
Protein turnover - damaged proteins have to be removed, regulation of protein activity also so get rid of those you dont need

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5
Q

what is the main problem for amino acid breakdown?

A

They contain Nitrogen in their side chains as well as their basic structure not all

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6
Q

What does the breakdown of amino acid produce?

A

Ammonia and ammonium ions, high concentrations these become toxic (contain nitrogen)

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7
Q

what is toxic at high levels?

A

Ammonium NH4+

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8
Q

What is the main nitrogen containing excreting molecule?

A

Urea - formed in liver, main excretion molecule for nitrogen, 80% excreted via urea

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9
Q

Where is urea produced?

A

In the LIVER

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10
Q

What is transamination? (CHECK)

A

First step in synthesis of urea

Amino acids are transferred to ketone acids
usually forms glutamic acid

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11
Q

What is de-amination? (CHECK)

A

Occurs only in the liver
Removal of amino acid from ketone acid
leaving alanine of glutamine

Free ammonium ion

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12
Q

What are the main transport molecules for nitrogen in the blood to the liver?

A

Alanine and glutamine

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13
Q

What is the final step of the urea cycle?

A

The ammonium enters the urea cycle

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14
Q

What is the remainder called once the amino group has been removed from the amino acid?

A

Carbon skeleton

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15
Q

What happens to the carbon skeletons?

A

They are converted to major metabolic intermediates

Or can be converted to glucose or oxidised in the TCA cycle

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16
Q

What are the different types of amino acids?

A

Ketogenic amino acids

Glucogenic amino acids

17
Q

Describe ketogenic amino acids

A

degrated to acetyl CoA or acetoacetly CAN give rise to ketone bodies or fatty acids CANNOT enter gluconeogenesis

18
Q

Describe glycogenic amino acids?

A

degraded to pyruvate or TCa cycle intermediated CAN be converted into phosphoenlopyruvate and then into glucose CAN enter gluconeogenesis