Amino Acid Nitrogen Flashcards

1
Q

What is the fate of most excess nitrogen?

A

it becomes urea

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2
Q

Fasting state - which two amino acids contribute to form glucose

A

alanine and glutamine

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3
Q

when muscle breaks down protein, most nitrogens come from

A

branched chains - valine, leucine, isoleucine.

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4
Q

Describe transamination reactions in general.

A

require PLP, use aminotransferases. more commonly needed for amino acid metabolism

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5
Q

Alanine transferase (ALT) give reactants and products

A

alanine turning into pyruvate

requires alpha ketoglutarate

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6
Q

Aspartate transaminase (AST)

A

aspartate turning into oxaloacetate, requires alpha ketoglutarate

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7
Q

Describe formation of PLP

A

pyradoxin, vitamin B6 starting material. oxidation of a primary alcohol into an aldehyde by a dehydrogenase. requires NAD+. Then a phosphate is transferred by a kinase.

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8
Q

What are two major carriers of nitrogen in the blood

A

alanine and glutamine

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9
Q

alpha amino acid becomes a keto acid; where does the oxygen come from?

A

water

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10
Q

alpha keto acid becomes alpha amino acid- where does the oxygen go?

A

goes to the water

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11
Q

branched-chain amino acid transaminase

A

branched chain amino acid plus alpha ketoglutarate becoming glutamate and branched chain ketoacid (3 different types of these). then those carbons can be used fuel - oxidize these branched chain keto acids.

works on all three branched chain amino acids.

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12
Q

glutamate dehydrogenase

A

glutamate getting oxidized into ammonia and alpha ketoglutarate using NADP+ or NAD+

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13
Q

glutamate synthetase

A

glutamate and ammonia ion with ATP becoming glutamine

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14
Q

glutaminase

A

glutamine + H2O becoming glutamate and ammonia ion. (for urea cycle)

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15
Q

Urea cycle - nitrogens show up as?

A

aspartate and ammonium ions

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16
Q

what enzymes are needed for liver to make aspartate and ammonium ion for the urea cycle?

A

glutamate dehydrogenase, glutaminase, aspartate transaminase

17
Q

ornithine transcarbamoylase

A

carbamoyl phosphate tranferred to ornithine to become citruline

18
Q

argininosuccinate synthetase

A

requires an ATP, combines arginine and aspartate.

19
Q

argininosuccinate lyase

A

argininosuccinate cleaved becoming fumarate and arginine

20
Q

arginase

A

hydroylysis reaction producing urea

REQUIRES MANGANESE as a cofactor

21
Q

what type of diet would have high level of ammonia

A

high protein

22
Q

what happens if urea cycle function is impaired

A

urea is toxic, personality changes, coma/death. can happen if liver disease

23
Q

Blood urea nitrogen test…

A

testing function for kidney failure

24
Q

breath urea test

A

testing for h pylori