Amino Acid and Protein Metabolism Flashcards

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1
Q

Explain the importance of dietary protein?

A
  • only some amino acids can be synthesised in the body, other need to be ingested
  • amino acids are required to make proteins and for neurotransmitters, nucleotides, creatine
  • they act as a source of blood glucose in fasting and starvation
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2
Q

What is the amino acid pool?

A

All the amino acids in the extracellular fluid.

They are free amino acids and they can mix and exchange with other free amino acids distributed throughout the body.

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3
Q

What is the average turnover of amino acids in the body per day?

A

300g-400g

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4
Q

Most proteins have a half life of a few days. Which protein is an exception?

A

Collagen

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5
Q

Can we store protein in the body?

What happens to surplus amino acids?

A

No storage form of protein

Surplus is rapidly catabolised and the nitrogen excreted as urea

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6
Q

How many amino acids do we rely on the diet to give us?

A

Half (10)

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7
Q

What are 3 essential amino acids we need to make?

A
  • alanine
  • aspartate
  • glutamate
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8
Q

What is a healthy nitrogen balance in an adult?

A

Total nitrogen intake should be equal to the total nitrogen excretion.

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9
Q

Give details on positive nitrogen balance

A
N intake > N excretion
Protein synthesis exceeds the rate of breakdown
During normal growth in children
In convalescence after serious illness
After immobilisation after an accident 
In pregnancy
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10
Q

Give details on negative nitrogen balance

A
N intake < N excretion
In starvation 
During serious illness
In late stages of some cancers
In injury and trauma 
If not corrected and becomes prolonged, there will be irreversible loss of essential body tissue and will ultimately lead to death
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11
Q

What happens in the degradation of most cellular proteins?

Foreign proteins?

A

cellular = recognised as old and removed by ubiqutin breakdown system giving a mixture of the 20 amino acids

Foreign exogenous protein - taken into vesicles by endocytosis or autophagocytosis, the vesicle fuses with lysosomes and proteolytic enzymes degrade proteins into amino acids

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12
Q

What is formed from amino acid degradation?

A

Pyruvate

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13
Q

What happens in oxidative deamination?

A

Water and a coenzyme is added to an amino acid and this forms a keto acid, ammonia and the coenzyme.

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14
Q

When transamination occurs, an amino acid is added to 2-oxaglutarate to form what?

A

an oxo acid and glutamate

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15
Q

What do all aminotransferases contain?

A

A tightly bound prosthetic group which is derived from vitamin B6 and it acts as a carrier of the amino group

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16
Q

What is the fate of oxo-acids?

A

Most of the amino acids become keto acids. They can be metabolised by the TCA pathway to carbon dioxide and water providing ATP. in starvation, 13 of the amino acids can be converted to glucose by the liver (glucogenic)

17
Q

What can leucine and lysine be converted to?

A

Acetyl CoA (ketogenic)

18
Q

What are the 3 fates of amino acids in rhe body?

A
  • excreted as urea
  • turned into special compounds such as neurotransmitters
  • turned to keto-acids to be used in TCA cycle
19
Q

What is the role of the liver in nitrogen metabolism?

A
  • removal of amino acids, glucose and fats from blood supply
  • absorbed amino acids used for synthesis of cellular proteins
  • synthesis of plasma proteins (albumin, clotting factors)
  • synthesis of haem and nucleotides
  • degradation of excess amino acids by trans deamination
  • conversion of ammonia to urea for excretion
20
Q

What tissue degrades proteins to amino acids?

How are the amino groups (NH2) transported in the blood stream?

A

Skeletal muscle

As glutamine

21
Q

If water is added to glutamine along with glutaminase, what happens?

A

Ammonia is released and glutamate is formed.

22
Q

What 4 amino acids are important in the inter-organ transport of nitrogen and explain one

A
  • alanine
  • glutamate
  • glutamine
  • aspartate

glutamine - safe carrier of ammonia in the blood. It can carry 2 ammonia equivalents to the lover for urea formation and can deliver ammonium ions to the kidney for pH regulation

23
Q

Review the urea cycle

A

Look up a diagram

24
Q

What are the end products of nitrogen metabolism?

A
  • urea (protein breakdown)
  • creatine (creatine phosphate breakdown)
  • uric acid (DNA and RNA breakdown)
  • ammonia (control of body pH)
25
Q

What can happen with an impaired conversion of ammonia to urea?

A

liver failure

genetic defects