Lecture 22 - Amino Acid Catabolism and the Urea Cycle Flashcards

1
Q

Overview of Amino Acid Catabolism

A

Normal synthesis and degradation of cell proteins
- rate of synthesis = rate of degradation
Excess amino acids if diet rich in protein
Starvation or Diabetes
- carbs not always available
- amino acids then used for fuel

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2
Q

How do we break down protein from diet?

A
Enzymes in stomach 
- pepsinogen 
- HCl
Enzymes in small intestine
- trypsinogen 
- chymotrypsinogen
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3
Q

Transport of Amino Acids across Membranes

A

Amino acids have specific protein carriers in membranes
Amino acid transport system is active transport
Requires energy
Maintains higher concentration of amino acids inside relative to outside of cell

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4
Q

What happens to N in amino acid oxidation?

A
Released from amino acid
Synthesis of:
- creatine
- transmitters
- purines
- pyrimidine
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5
Q

What happens to C (from C skeleton) in amino acid oxidation?

A

Can be synthesised as:

  • glucose
  • glycogen
  • fatty acids
  • steroids
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6
Q

What happens to the ammonium produced from the breakdown of amino acids?

A

Incorporated into ammonium containing molecules

Can be utilised to form Carbamoyl phosphate which then enters urea cycle

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7
Q

Removal of Amino Group

A

Transamination
- transfer and removal of a-amino group from amino acid to a-keto acid
Glutamate Dehydrogenase
- removal of a-amino group from glutamate to free ammonium and a-ketoglutarate
Glutaminase
- removal of amino group from side chain of glutamine to glutamate and free ammonium

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8
Q

Transaminase Reactions

A

Facilitate transfer of amino groups from one compound to another
Reversible
Takes place in liver

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9
Q

How do tissues and muscles decrease levels of ammonium?

A

Extrahepatic tissues convert ammonium into glutamine for transport by blood to liver
Muscles convert ammonium to alanine, via glucose-alanine cycle, for transport by blood to liver

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10
Q

Ammonium Transporters

A
Glutamine
- between tissues
Glutamate
- within tissues and between cytosol and mitochondria
Alanine 
- principally between muscle and liver
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11
Q

Which amino acids are ketogenic?

A
Tyrosine
Isoleucine
Phenylalanine
Tryptophan 
Leucine
Lysine
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12
Q

What does it mean for an amino acid to be ketogenic or glucogenic?

A

Ketogenic - amino acid that can be degraded directly into acetyl-CoA
Glucogenic - amino acid that can be converted to glucose through gluconeogenesis

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