Chapter 18 Part 2 Flashcards

1
Q

Glycogenic Amino Acids

A
  • Arginine
  • Glutamine
  • Histidine
  • Proline
  • Isoleucine
  • Methionine
  • Threonine
  • Valine
  • Phenylalanine
  • Asparagine
  • Aspartate
  • Alanine
  • Cysteine
  • Glycine
  • Serine
  • Tryptophan
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2
Q

Ketogenic Amino Acids

A
  • Isoleucine
  • Leucine
  • Threonine
  • Tryptophan
  • Lysine
  • Phenylalanine
  • Tyrosine
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3
Q

Name a common function in amino acid catabolism.

A

One-carbon transfers

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4
Q

One-carbon transfer enzyme cofactors

A
  1. Biotin
  2. Tetrahydrofolate
  3. S-adenosylmethionine
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5
Q

Biotin Transfer

A

Transfers CO2, carbon in its most oxidized state

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6
Q

Tetrahydrofolate Transfer

A

Transfers carbon in intermediate oxidized states and -CH3 groups, the most reduced state

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7
Q

S-adenosylmethionine Transfer

A

Transfers -CH3 groups

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8
Q

Tetrahydrofolate

A
  • derivative of folate (vitamin)
  • the one carbon group undergoing transfer is bonded to N-5 or N-10 and is carried as a methyl, methylene, methanol, formyl or formimino group.
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9
Q

S-adenosylmethinonine

A
  • preferred cofactor for biological methyl group transfers
  • 1000 times more reactive then the N-5 group of tetrahydrofolate
  • derived from ATP and methionine
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10
Q

Six amino acids degraded to pyruvate

A
  • A, C, G, S, T and W
  • converted directly to pyruvate
  • can then be converted to oxaloacetate or acetyl-CoA
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11
Q

T and G’s conversion to pyruvate

A

facilitated by tetrahydrofolate

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12
Q

Seven amino acids degraded to acetyl-CoA

A
  • Portions of W, K, F, Y, L, I and T
  • ketogenic amino acids
  • end result of acetyl-CoA can be ketone bodies
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13
Q

F and Y conversion to fumarate

A

other portions of F and Y are converted to fumarate to feed TCA or gluconeogenesis

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14
Q

Five amino acids converted to α- ketoglutarate

A
  • Portions of P, E, Q, R and H

- H is the only amino acid that requires a cofactor, in the final step a carbon is passed to tetrahydrofolate

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15
Q

Four amino acids are converted to succinyl-CoA

A
  • Portions of M, I, T and V
  • ultimately produce propionyl-CoA which is converted to succinyl-CoA
  • M donates its -CH3 to S-adenosylmethionine
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16
Q

Propionyl-CoA to succinyl-CoA

A

converted via odd chain fatty acid oxidation

17
Q

Branched chain amino acids

A
  • In muscle, adipose, kidney and brain L, I and V are oxidized as fuels
  • aminotransferases remove the amino group and α- kept acid dehydrogenase complexes the oxidative decarboxylation and formation of acyl-CoA derivatives
18
Q

N and G converted to oxaloacetate

A

-converted to oxaloacetate and enter the citric acid cycle and gluconeogenesis

19
Q

Amino acid degradation to reducing equivalents

A

the degradation of amino acids ultimately results in the generation of reducing equivalents (NADH and FADH2) which feed oxidative phosphorylation