1.11 - Amino Acid Metabolism Flashcards

(34 cards)

1
Q

functions of muscle in protein metabolism (4)

A
  1. reservoir of amino acids
  2. major site of muscle protein break-down
  3. utilises branched chain amino acids (BCAAs) as fuel source
  4. can provide crucial precursors for gluconeogenesis during times of fasting (glucose-alanine cycle)
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2
Q

what happens if pyruvate isnt eliminated?

A

lactic acid build up

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3
Q

how can pyruvate be transported to liver? (2)

A
  1. pyruvate converted to alanine
  2. transported to liver via cardiovascular system
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4
Q

transamination

A

transfer of amino group to a ketoacid to produce new amino acid

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5
Q

purpose of amino group removal

A

to make carbon skeleton available as metabolic intermediate

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6
Q

how are the toxic amino group/ammonia (NH4) dealt with?

A

transfer to ketoacid intermediate (transamination)
(such as pyruvate, a-ketoglutarate and oxaloacetate)

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7
Q

pyruvate conversion to alanine (transamination)

A

pyruvate accepts amine group from glutamate

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8
Q

What is given as a result of glutamate donating amine to pyruvate

A

a-ketoglutarate

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9
Q

when can a-ketoglutarate be used in muscle?

A

if theres enough N

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10
Q

why is alanine less likely to affect blood pH?

A

it is a neutral amino acid

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11
Q

cori cycle

A

lactic acid transported back to liver to be converted back to glucose (gluconeogenesis)

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12
Q

how is alanine converted back to pyruvate in the liver?

A

alanine donates amine group to a-ketoglutarate producing pyruvate and glutamate (transamination)

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13
Q

what is given as a result of a-ketoglutarate accepting an amine group from alanine (liver)

A

glutamate (will enter urea cycle)

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14
Q

alanine aminotransferase

A

transfers amino group (NH3+) from alanine to a-ketoglutarate

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15
Q

metabolic intermediates produced in the reaction of a-ketoglutarate accepting an amino group from alanine (2)

A
  1. pyruvate
  2. glutamate
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16
Q

amino acid metabolism during short term starvation in an absence of fatty acids to feed into TCA, or glucose (2)

A
  1. tissue broken down -> amino acid constituents
  2. amino acids catabolised -> carbon skeletons (feed into intermediary metabolism to give energy)
17
Q

glutamine and alanine role in allowing liver to maintain blood glucose

A

crucial in transporting amino groups around the body

18
Q

major amino acid in muscle protein

A

branched chain amino acid (BCAA) leucine

19
Q

how is a-ketoglutarate converted to glutamate

A

ammonia ion received

20
Q

alanine, glutamate and glutamine fundamental function

A

transporting ammonia/nitrogen around body

21
Q

how can glucose be supplied to muscle (constant glycolysis) (2)

A
  1. via CVS from plasma
  2. solubilised from glycogen store
22
Q

primary mechanism for skeletal muscle to eliminate nitrogen while replenishing energy via BCAAs (3)

A
  1. if BCAA present in plasma (diet) - muscle cells use them as fuel
  2. resulting ammonium ions stored in forms of glutamate, glutamine and alanine
  3. ideal forms of amino acids to be transported via CVS
23
Q

what is alanine fuel for?

A

gluconeogenesis (via pyruvate) in liver

24
Q

glucose-alanine cycle (3)

A
  1. during periods of fasting, skeletal muscle protein degraded -> amino acid constituents
  2. ultimately processed -> alanine, transported in blood to liver
  3. alanine fuels gluconeogenesis (via pyruvate) in liver -> glucose -> back to muscle
25
what amino acid constituents in muscle protein are used as fuel?
carbon skeleton (and other BCAAs)
26
how do most other tissues get carbon skeletons from amino acids?
use amino acid deaminases to catabolise amino acids -> carbon skeletons
27
why is glutamine good for transporting amino groups around body?
can come from any tissue in body
28
role of glutamine in ammonia ion group excretion
glutamine transported to kidney where it feeds into the urea cycle (glutamine cycle)
29
role of intrinsic structural relationship between amino acids and metabolic intermediates
means cells can do reverse and use metabolites to produce amino acids
30
crucial event in processing amino acids -> hormones
decarboxylation
31
cofactor of all decarboxylases
pyridoxal 5' phosphate (PLP)
32
what does the decarboxylase reaction result in?
Removal of CO2
33
glutamine to GABA neurotransmitter (4)
1. glutamine taken up into neurons 2. processed -> glutamate by glutaminase 3. glutamate decarboxylated -> GABA by glutamate decarboxylase 4. GABA packaged into vesicles and released into synaptic cleft
34
role of tyrosine in maintaining neuronal signalling (2)
1. tyrosine taken into neuron, converted -> DOPA 2. aromatic amino acid decarboxylase (AAAD/AADC) produces dopamine (can either signal or turned over by monoamine oxidase (MAO))