Amino acid metabolism Flashcards

1
Q

What is the concentration of free amino acids in plasma?

A
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2
Q

Where do free amino acids come from?

A

Degradation of dietary protein
Synthesis of some proteins
Degradation of endogenous protein

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3
Q

For what are free amino acids used?

A

For resynthesis of endogenous proteins
Energy production
As precursors for other biological pathways

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4
Q

What happens in essential amino acid deficiency?

A

Since proteins require pretty much every amino acid, a missing or inadequate intake of a single amino acid can stunt growth in children or lead to protein breakdown in adults

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5
Q

Two primary pathways for protein degradation

A

ATP-dependent ubiquitin-proteasome system and lysosomal pathway

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6
Q

Relative breakdown time of regulatory proteins

A

Tend to be degraded and resynthesized faster than other proteins

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7
Q

How much protein is lost every day and must be re-supplied by diet?

A

55 g

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8
Q

What are examples of body states that would require positive nitrogen balance?

A

Growth in children, pregnancy, bodybuilding

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9
Q

Major regulated step in the synthesis of urea

A

Synthesis of carbamoyl phosphate

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10
Q

Where does urea biosynthesis occur?

A

In the liver

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11
Q

Transamination

A

Transfer of the amino group to AKG to form glutamate

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12
Q

Cofactor required for transaminases

A

Pyridoxal phosphate (derivative of B6)

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13
Q

Alanine transaminase blood levels

A

Shows some sort of inflammation in the liver mostly, as well as some in the pancreas and kidney

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14
Q

Aspartate transaminase blood levels

A

Shows inflammation/pathology somewhere.

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15
Q

Aspartate transaminase

A

Glutamate that was just formed donates its nitrogen side chain to oxaloacetate, creating aspartate

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16
Q

Glutamate dehydrogenase

A

NADP/NAD+ reduces glutamate to alphaketoglutarate and releases the nitrogen group to make ammonium

17
Q

Major regulated step in the synthesis of urea

A

Synthesis of carbamoyl phosphate

18
Q

What is absolutely required in the formation of carbamoyl phosphate?

A

N-acetylglutamate

19
Q

Overall reaction of the formation of urea

A

Aspartate + ammonia + CO2 + 3 ATP + 3 H2O -> urea + fumarate + 2 ADP + AMP + 4 Pi

20
Q

Where do things take place during urea formation?

A

Formation of carbamoyl phosphate and citrulline take place in the mitochondria. The others are in the cytosol.

21
Q

Control of the urea cycle

A

The amount of glutamate, which is higher postprandially, will lead to higher amounts of N-acetylglutamate and increase the activity of the urea cycle

22
Q

Main carriers of nitrogen to the liver

A

Alanine and glutamine

23
Q

Hyperammonemia

A

Too high of concentration of ammonia in the blood, which predisposes to coma

24
Q

Acquired hyperammonemia

A

Usually due to shunting of blood around the liver due to cirrhosis; ammonia produced from bacteria in the intestines is not converted to urea. Leads to “portal-systemic encephalopathy.”

25
Q

Ketogenic amino acids

A

Leucine and lysine

26
Q

Amino acids that are both ketogenic and glucogenic

A
Tyrosine
Tryptophan
Threonine
Isoleucine
Phenylalanine