week 3 nitrogen Flashcards

1
Q

do carbohydrates and fats contain nitrogen

A

no

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2
Q

do amino acids and nucleotides contain nitrogen

A

yes

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3
Q

what are the main nitrogen-containing molecules in the body

A

amino acids and nucleotides

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4
Q

where do we get nitrogen from

A

our diet (not air!!!)

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5
Q

how are dietary proteins enzymatically hydrolysed

A
  • pepsin cuts protein into peptides in the stomach
  • trypsin and chymotrypsin cut proteins and larger peptides into smaller peptides in the small intestine
  • aminopeptidase and carboxypeptidases A and B degrade peptides into amino acids in the small intestine
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6
Q

what is enzymatic degradation of dietary proteins

A

dietary proteins being degraded to form amino acids

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7
Q

where do you get enzymatic degradation of dietary proteins

A
  • gastric glands in stomach lining
  • exocrine cells of pancreas
  • villi of small intestine
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8
Q

how many essential amino acids

A

9
histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan and valine
- these cannot be made in the body so we have to get them from diet

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9
Q

why can cellular proteins sometimes be targeted for destruction

A

sometimes misfolded proteins, foreign proteins and unwanted proteins are degraded for their amino acids

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10
Q

what does the urea cycle do

A

takes ammonia and turns it into urea

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11
Q

how do we get ammonia in the body

A

amino acid metabolism results in the formation of ammonia
- if ammonia is present in too high a concentration it is toxic so this is why it is turned into urea (in the liver) which isn’t very toxic and can be excreted in urine

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12
Q

how is nitrogen transferred to, from and between amino acids

A

by oxidative deamination and transamination (aminotransfer) reactions involving glutamate.

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13
Q

what is special about glutamate

A

only amino- acid that can obtain its nitrogen directly from ammonium ions.

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14
Q

how is nitrogen transported through plasma to liver

A

as glutamine

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15
Q

how is nitrogen transported from skeletal muscle

A

as alanine

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16
Q

what is the fate of the carbon of catabolised body protein

A

Carbon of turned- over amino-acids may be used to form intermediates of glycolysis, gluconeogenesis, citric acid cycle or lipid metabolism pathways

17
Q

what is PKU

A

Phenylketonuria results from a genetic defect in the enzyme responsible for hydroxylating phenylalanine.