Catabolism for energy production Flashcards

1
Q

amino acid uptake and catabolism occurs mainly where?

A

in the liver (only partial oxidation)

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2
Q

where can oxidation of amino acids occur? (get ATP from amino acids)

A
  • liver
  • muscles
  • jejenum
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3
Q

branched-chain amino acids are catabolized _________ in the liver than in the muscles.

A

SLOWER

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4
Q

In the liver, which amino acids are uptaken alot (high uptake) and which are not taken up as much (lower uptake)

A

Alanine and serine= high uptake

Aspartate and glutamate = low uptake

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5
Q

what is transamination?

A

Transamination is the transfer of amino group to an a-keto acid to form another amino acid by the enzyme aminotransferase/transaminase.

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6
Q

which are the most active aminotransferases??

A

alanine and aspartate aminotransferase

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7
Q

what amino acid is formed by pyruvate? oxaloacetate?

A

alanine from pyruvate

aspartate from oxaloacetate

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8
Q

which a.a’s do not participate directly in transamination?

A

lysine, tryptophan, proline, arginine

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9
Q

what is deamination? is it common?

A

Deamination is removal of an a-amino group from amino acid to release NH3 and form a keto acid. It is less common than transamination

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10
Q

what is the most common deamination in the body?

A

conversion of glutamate to a-ketoglutarate and NH3 (catalyzed by glutamate dehydrogenase)

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11
Q

where is glutamate dehydrogenase present in high activity?

A

liver, brain and kidney cortex

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12
Q

How is ammonia (NH3) disposed of in the liver, brain and kidney??

A

liver: NH3–> Urea
brain: NH3–> glutamine
kidney: NH3–> excreted in urine

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13
Q

which amino acid is involved in ammonia transport?

A

Glutamine

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14
Q

what is the carbon skeleton of amino acids used for?

A
  • energy (when diets low carbs)
  • keton bodies
  • fatty acids
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15
Q

what is ureagenesis?

A

Formation of urea by the metabolism of amino acids to urea

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16
Q

what is the role of aspartate in ureagenesis?

A

serves as 2-carbon donor for ureagenesis

17
Q

catabolism of ketogenic amino acids produces what?

A

acetyl CoA or acetoacetate

18
Q

what are the only totally ketogenic amino acids?

A

lysine and leucine

19
Q

which amino acids are both gluconeogeneic and ketogeneic?

A
threonine
isoleucine
phenylalanine
tryptophan
tyrosine
20
Q

which amino acids are gluconeogenic?

A

Glycine, serine, valine, histidine, arginine, cysteine, proline, alanine, glutamate, glutamine, aspartate, asparagine, methinoine

21
Q

which groups of amino acids are likely to be metabolized into pyruvate?

A

Alanine, cysteine, glycine, serine, threonine, & tryptophan

22
Q

which amino acids are likely to be metabolized into a-ketoglutarate?

A

arginine, glutamate, glutamine, histidine, proline

23
Q

which amino acids are metabolized into succinyl-CoA ?

A

isoleucine, methionine, threonine, valine

24
Q

which amino acids are metabolized into fumarate?

A

phenylalanine, tyrosine

25
Q

which amino acids are metabolized into oxaloacetate?

A

asparasgine and aspartate