Nitrogen Flashcards

exam 4 (55 cards)

1
Q

present in AA and when AA get degrades it has two fates

A

nitrogen

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2
Q

nitrogen components can be used to

A

create nitrogen containing compounds like heme or is excreted as urea

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3
Q

under conditions of constant weight, ureas

A

is the only paarameter that changes according to protein intake

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4
Q

balanced nitrogen levels

A

not gaining muscle or protein

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5
Q

positive nitrogen levels

A

overall increase in body protein

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6
Q

negative nitrogen levels from trauma

A

higher loss of body protein and more urea excretion

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7
Q

negative nitrogen levels from insufficient protein/dietary protein

A

loss of body protein to A.A. pool

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8
Q

ammonia regeneration in

A

liver

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9
Q

ammonia is incorporate to

A

urea

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10
Q

transfer of nitrogen to

A

common carrier

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11
Q

catalyzes reaction of alpha-ketoglutarate nad AA

A

aminotransferase

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12
Q

alpha-keto and AA forms

A

glutamate and alpha-keto acid

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13
Q

cofactor in reaction of alpha-keto to glutamate

A

PLP

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14
Q

PLP is derived from vitamin

A

B6

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15
Q

catalyzes rxn of glutamate to alpha-ketogluturate and ammonia

A

glutamate DH

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16
Q

Glutamate DH occurs in the

A

mitochondria

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17
Q

Glutamate DH produces

A

NADH

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18
Q

Glutamate DH is inhibited by

A

energy rich

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19
Q

Glutamate DH is activated by

A

low energy

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20
Q

there is only one reaction that can form ammonia

A

FALSE: a few different one

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21
Q

ammonia can be excreted in three ways

A
  1. run Glutamate DH in reverse
  2. Create Glutamine via Glutamine synth
  3. urea cycle
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22
Q

when glutamte DH is done in the reverse and creates glutamate it consumes

A

NH4+

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23
Q

is a central intersection of the urea cycle

24
Q

the creation or consumption of glutamate results in the formation of

25
reaction of glutamine to glutamate via glutaminase results in
NH4+
26
alanine or AA can turn into glutamate in cytosol
coming from muscle by Cori/cahill cycle
27
reacts later on in urea cycle to donate NH4+
aspartate
28
reaction of aspartate aminotransferase react glutamate + OAA to form
alpha-keto and aspartate
29
combines in the mitochondria with ornithine and ornithine transcarbamoylase
carbamoyl phosphate
30
carbamoyl phosphate + ornithine -->
citrulline
31
citrulline leaves the mitochondria by
ATP dependent transport
32
citrulline in the cytoplasm combines with aspartate to make
argininosuccinate
33
enzyme that is used to catalyze the reaction between citrulline and aspartate
argininosuccinate synthase
34
argininosuccinate is broken by
argininosuccinase
35
argininosuccinate is broken down to
fumarate and arginine
36
arginine is broken down by
arginase
37
arginine is broken to produce _________ and regenerate _______
urea and regenerate ornithine
38
reenters the mitochondria to start cycle
ornithine
39
urea has
2 ammonia molecules
40
urea ammonia comes from
NH4+ and from aspartate
41
CPSI is strongly promoted by
N-acetyl glutamate
42
strong promoter of N-acetyl glutamate
arginine
43
dysfunction of NAGs leads to low activated of CPSI
NAGS deficiency
44
carbaglu
treats NAGs deficinecy
45
CPSI catalyzes the reaction between CO2 and NH4+ and 2 ATP to form
carbamoyl phosphate
46
developmental delays, cognitive delays, seizures, protein intolerance
genetic defects of urea cycle
47
tx for defects in urea cycle
- low protein diet | - increase nitrogen excretion
48
acts as a product and substrate of the urea cycle
ornithine
49
can react with alpha-ketoglutarate to form glutamate via glutamic x-semialdehyde
orntihine
50
glutamic x-semialdehyde can be turned into
proline
51
ornithine can be used to create
Arginine
52
arginine is used to make
NO and creatine
53
can be used to make polyamines
ornithine
54
is the one that binds DNA in sperm
spermine
55
arginine, ornithine, glutamate/glutamine and proline are all
metabolically linked