Nitrogen Flashcards
exam 4
present in AA and when AA get degrades it has two fates
nitrogen
nitrogen components can be used to
create nitrogen containing compounds like heme or is excreted as urea
under conditions of constant weight, ureas
is the only paarameter that changes according to protein intake
balanced nitrogen levels
not gaining muscle or protein
positive nitrogen levels
overall increase in body protein
negative nitrogen levels from trauma
higher loss of body protein and more urea excretion
negative nitrogen levels from insufficient protein/dietary protein
loss of body protein to A.A. pool
ammonia regeneration in
liver
ammonia is incorporate to
urea
transfer of nitrogen to
common carrier
catalyzes reaction of alpha-ketoglutarate nad AA
aminotransferase
alpha-keto and AA forms
glutamate and alpha-keto acid
cofactor in reaction of alpha-keto to glutamate
PLP
PLP is derived from vitamin
B6
catalyzes rxn of glutamate to alpha-ketogluturate and ammonia
glutamate DH
Glutamate DH occurs in the
mitochondria
Glutamate DH produces
NADH
Glutamate DH is inhibited by
energy rich
Glutamate DH is activated by
low energy
there is only one reaction that can form ammonia
FALSE: a few different one
ammonia can be excreted in three ways
- run Glutamate DH in reverse
- Create Glutamine via Glutamine synth
- urea cycle
when glutamte DH is done in the reverse and creates glutamate it consumes
NH4+
is a central intersection of the urea cycle
glutamate
the creation or consumption of glutamate results in the formation of
NH4+
reaction of glutamine to glutamate via glutaminase results in
NH4+
alanine or AA can turn into glutamate in cytosol
coming from muscle by Cori/cahill cycle
reacts later on in urea cycle to donate NH4+
aspartate
reaction of aspartate aminotransferase react glutamate + OAA to form
alpha-keto and aspartate
combines in the mitochondria with ornithine and ornithine transcarbamoylase
carbamoyl phosphate
carbamoyl phosphate + ornithine –>
citrulline
citrulline leaves the mitochondria by
ATP dependent transport
citrulline in the cytoplasm combines with aspartate to make
argininosuccinate
enzyme that is used to catalyze the reaction between citrulline and aspartate
argininosuccinate synthase
argininosuccinate is broken by
argininosuccinase
argininosuccinate is broken down to
fumarate and arginine
arginine is broken down by
arginase
arginine is broken to produce _________ and regenerate _______
urea and regenerate ornithine
reenters the mitochondria to start cycle
ornithine
urea has
2 ammonia molecules
urea ammonia comes from
NH4+ and from aspartate
CPSI is strongly promoted by
N-acetyl glutamate
strong promoter of N-acetyl glutamate
arginine
dysfunction of NAGs leads to low activated of CPSI
NAGS deficiency
carbaglu
treats NAGs deficinecy
CPSI catalyzes the reaction between CO2 and NH4+ and 2 ATP to form
carbamoyl phosphate
developmental delays, cognitive delays, seizures, protein intolerance
genetic defects of urea cycle
tx for defects in urea cycle
- low protein diet
- increase nitrogen excretion
acts as a product and substrate of the urea cycle
ornithine
can react with alpha-ketoglutarate to form glutamate via glutamic x-semialdehyde
orntihine
glutamic x-semialdehyde can be turned into
proline
ornithine can be used to create
Arginine
arginine is used to make
NO and creatine
can be used to make polyamines
ornithine
is the one that binds DNA in sperm
spermine
arginine, ornithine, glutamate/glutamine and proline are all
metabolically linked