nitrogen metabolism Flashcards

1
Q

Where do we get nitrogen?

A

Plants and Animals

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2
Q

How do we get nitrogen from plants?

A

obtained from nitrogen-fixing bacteria (N2 to NH3)

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3
Q

Do plants use amino acids for energy?

A

no

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4
Q

How do we get nitrogen from animals?

A

Carnivores, Herbivores, and Cellular proteins (amino acid catabolism)

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5
Q

What are the enzymes to break down dietary proteins?

A

Pepsin and zymogens

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6
Q

Where is pepsin found?

A

in stomach

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7
Q

Where are zymogens released?

A

released from exocrine cells in pancreas and get processed into active proteases

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8
Q

What are the three zymogens from the pancreas?

A

Trypsinogen, Chymotrypsinogen, and Procarboxypeptidase

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9
Q

What is the pro-form of pepsin?

A

Pepsinogen

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10
Q

What are the three cleaved active zymogens?

A

trypsin, chymotrypsin, and carboxypeptidase

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11
Q

What do ketogenic amino acids enter the TCA cycle as?

A

acetyl coA

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12
Q

What do glucogenic amino acids enter the TCA cycle as?

A

oxaloacetate

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13
Q

What are the true ketogenic amino acids?

A

leucine, lysine

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14
Q

What amino acids enter as acetyl-coA and what is their classification?

A

leucine, lysine, phenylalanine, tryptopahn, tyrosine, isoleucine, and threonine
Ketogenic Amino acids

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15
Q

What amino acids enter as oxaloacetate and what is their classification?

A

alanine, cysteine, glycine, serine, threonine, and tryptophan, asparagine, and aspartate
Glucogenic

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16
Q

What amino acids enter as fumarate and what is their classification?

A

phenylalanine and tyrosine
glucogenic

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17
Q

What amino acids enter as Succinyl-coA and what is their classification?

A

Isoleucine, methionine, threonine, and valine
Glucogenic

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18
Q

What amino acids enter as glutamate to a-ketoglutarate and what is their classification?

A

arginine, glutamine, histidine, and proline
Glucogenic

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19
Q

What is an ammonotelic and an example of an organism?

A

organism that excretes N2 in the form of ammonia
example: bony fish, except sharks

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20
Q

What is a ureotelic and an example of an organism?

A

Organism that excretes urea
example: humans and sharks

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21
Q

What is a uricotelic and an example of an organism?

A

Organism that excretes uric acid
example: birds and reptiles

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22
Q

What is the primary intermediate amino acid before entering the urea cycle

A

glutamate

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23
Q

Where does the processing of ammonia to products primarily occur?

A

In the liver

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24
Q

What is the role of Glutamine?

A

replaces the O- with ammonia group m(NH3), by removing acid acting properties of glutamate

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25
What does not transport well in the blood due to the carboxyl R group?
glutamate
26
What facilitates the transfer of oxygen group to ammonia group?
glutamine synthetase
27
What inhibits glutamine synthetase?
Alanine, Glycine, AMP, and Carbamoyl Phosphate
28
What facilitates the transfer of an amino group from glutamate onto pyruvate to give alanine?
alanine aminotransferase
29
What facilitates the transfer from alanine onto a-ketoglutarate to glutamate and creates pyruvate?
alanine aminotransferase
30
What coenzyme does aminotransferase need?
PLP (pyridoxal phosphate) form of a vitamin B6
31
What enzyme removes ammonia from glutamate and releases a-ketoglutarate?
glutamate dehydrogenase
32
What enzyme facilitates the addition of the ammonia group onto a carbon skeleton producing carbamoyl phosphate?
carbamoyl phosphate synthetase I
33
How many ATP to make carbamoyl phosphate?
2 ATP
34
What is the main connection between the Urea and TCA cycle?
Krebs Bicycle - Aspartate-argininosuccinate shunt
35
What is the function of the malate aspartate shuttle?
regenerate NADH in the mitochondira
36
What is the main point of regulation in the Urea Cycle
N-Acetylglutamate
37
Regulation of the Urea cycle with fasting?
protein breakdown
38
Regulation of the Urea cycle with High protein diet?
extra nitrogen decomposed & excreted
39
What birth defect is the defective process of melanin synthesis from tyrosine?
Albinism
40
What is the defective enzyme of Albinism?
Tyrosine 3-monooxygenase
41
What are the symptoms of Albinism?
Lack of pigmentation; white hair, pink skin
42
What defect is the defective process of urea synthesis?
Carbamoyl phosphate synthetase I deficiency
43
What is the defective enzyme of Carbamoyl phosphate synthetase I deficiency?
carbamoyl phosphate synthetase I
44
What are the symptoms of carbamoyl phosphate synthetase I deficiency?
lethargy; convulsions; early death
45
What defect is the defective process of isoleucine, leucine, and valine degradation?
Maple syrup urine disease
46
What is the defective enzyme of maple syrup urine disease?
branched-chain a-keto acid dehydrogenase complex
47
What are the symptoms are maple syrup urine disease?
vomiting; convulsions; intellectual disability; early disease
48
What is the defective process of the conversion of phenylalanine to tyrosine?
Phenylketonuria
49
What is the defective enzyme of phenylketonuria?
phenylalanine hydroxylase
50
What are the symptoms of phenylketonuria?
neonatal vomiting; intellectual disability
51
What are alternative pathways for nitrogen excretion?
treat with benzoate and/or phenylbutyrate
52
What amino acid is used with benzoate and how many nitrogens are excreted?
glycine 1 nitrogen
53
What amino acid is used with Phenylbutyrate and how many nitrogens are excreted?
glutamine 2 nitrogens
54
What is the build up and loss of molecules in maple syrup urine disease?
build up of a-keto acids and loss of nitrogens
55
What does phenylalanine hydroxylase mediate?
The transfer of and OH from phenylalanine to make tyrosine
56
What pathway requires extensive e- transfers?
Nitrogen fixation
57
How many ATP are required per N2 molecule in Nitrogen fixation?
16 ATP
58
What is the starting transfer in the fixation of nitrogen?
4 coA + 4 pyruvate to 4 CO2 + 4 acetyl-coA
59
What is the end transfer in the fixation of nitrogen?
N2 + 2H to 2NH4 + H2
60
Amino acid synthesis summarized?
Make carbon skeleton first, then transamination reaction to add amino group
61
Can animals synthesize essential amino acids?
NO