Q 7: Protein Metabolism: Oxidation & Urea - German Flashcards

(33 cards)

1
Q

What are the four fates of dietary amino acids?

A

Protein synthesis

Energy production (Citric Acid Cycle)

Biosynthesis

Urea Excretion

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2
Q

What are the three drivers of protein oxidation?

A

Normal synthesis and degradation

Protein rich diet

Starvation or diabetes mellitus

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3
Q

Why are proteins broken down if they’re not immediately used?

A

There is no way to store amino acids/proteins

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4
Q

What is an enzyme precursor that requires a biochemical change for activation (usually cleavage)?

A

Zymogen

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5
Q

What are the pancreatic zymogens?

A

Trypsinogen —> trypsin

Chymotrysinogen —> chymotrypsin

Procarboxypeptidase A and B —> carboxypeptidase A and B

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6
Q

What does trypsin do?

A

It cleaves chymotrypsinogen into chymotrypsin

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7
Q

What are the fates of amino acids?

A

Used for protein and biosynthesis within cells

Catabolized for energy within cells

Transported to the liver and excreted

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8
Q

What does dietary protein lead to (referring to the cascade of hormones)?

A

Dietary protein —> gastrin secretion —> HCl release —> pH drop

Dietary protein —> gastrin secretion —> pepsinogen —> pepsin, secretin, and cholecystokinin release

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9
Q

What does pepsin do?

A

.

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10
Q

What does secretin do?

A

.

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11
Q

What does cholecystokinin do?

A

.

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12
Q

Where does most amino acid catabolism take place?

A

Liver

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13
Q

What are the metabolically important amino acids?

A

Glutamate

Aspartame

Glutamine

Alanine

(Amine group carriers, precursors and common metabolites, and entry and exit molecules from the citric acid cycle)

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14
Q

Ammonia is toxic to all animals except?

A

Aquatic animals/fish? They secrete ammonia

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15
Q

What are symptoms of ammonia buildup in mammals?

A

.

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16
Q

NH4+ does what in the brain?

A

Disrupts astrocyte K+ uptake

17
Q

What happens when you get high extracellular K+ in the brain?

A

GABA inhibition is prevented

Leads to neuronal hyperactivity, seizures, oxidative stress, death

18
Q

How have animals developed to prevent NH4+ problems in the brain?

A

The body keeps NH4+ levels in the blood relatively low.

Vertebrates create stable molecules of UREA to avoid NH4+ probs

Birds turn it into uric acid

19
Q

What are transaminase reactions?

A

They move amine groups from one ketoacid to another (the new amino acids often become amine carriers)

20
Q

What happens when you add an amine group to glutamate?

A

You get glutamine

21
Q

What makes glutamine a common synthetic precursor?

A

Its ability to transport NH4+

22
Q

What allows proteins to function as energy sources?

A

Glucose-alanine cycle (G-A cycle)

(It will use pyruvate from glycolysis and turn it into alanine which is shuttled to the liver and used in gluconeogenesis to generate glucose)

23
Q

What amino acids feed into fumarate in the CAC?

A

Phenylalanine

Tyrosine

24
Q

What is a glucogenic amino acid?

A

Amino acid that can be converted to glucose

25
What is a ketogenic amino acid?
Amino acid that can be converted to ketone bodies (broken down into acetyl-CoA)
26
Which amino acid can become pyruvate or succinyl-CoA?
Threonine
27
What AA are broken down into pyruvate?
Alanine Cysteine Glycine Serine Threonine Tryptophan
28
What AA are broken down into oxaloacetate?
Asparagine Aspartate
29
What AA’s are both glucogenic and ketogenic?
Threonine, isoleucine, tryptophan, phyenylalanine, tyrosine
30
Which AA is a one-step reaction to a-ketoglutarate?
Glutamate!!!!!
31
What AA’s become succinyl-CoA? How much energy does this produce (least, middle, most)?
Methionine Isoleucine Valine Threonine (Middle-low ish)
32
What are the AA’s that become a-ketoglutarate? How much energy does this produce (least, middle, most)?
Glutamate Glutamine Proline Arginine Histidine (Middle ish)
33
What are the AA’s that become Acetyl-CoA? How much energy does this produce (least, middle, most)?
Tryptophan Lysine Phenylalanine Tyrosine Leucine Isoleucine Threonine (Most energy from AA’s)