Protein metabolism Flashcards

1
Q

Explain the digestion and absorption of protein

A

> Protein digestion starts in the stomach – involves denaturation and hydrolysis of peptide bonds

> Pepsin (enzyme) hydrolyzes about 10% peptide bonds

> Small batches of acidic chyme containing large polypeptides enter the small intestine

> Bicarbonate ions help neutralise the acidic chyme and allow activation of enzymes that break peptide bonds liberating amino acids

> The “free” amino acids are absorbed via the intestinal wall into the bloodstream

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2
Q

What are the 3 sources of Amino Acids in the AA pool in the body?

A

Dietary protein

Protein turnover

Biosynthesis of nonessential AAs in the liver

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3
Q

What is nitrogen balance?

A

When the amount of nitrogen taken into the body as protein = the amount of nitrogen excreted from the body in waste materials

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4
Q

HCl functions in stomach?

A

 Denatures proteins, exposing peptide bonds
 Kills most bacteria (pH = 1.5-2.0)
 Activates pepsinogen (inactive zymogen) to active pepsin enzyme

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5
Q

Pancreatic enzymes activated in small intestines for peptide bond cleavage?

A
  • Trypsin
  • Chymotrypsin
  • Carboxypeptidase
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6
Q

Name the 3 steps needed to remove a =NH2 group?

A
  • Transamination
  • Oxidative Deamination
  • The Urea Cycle
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7
Q

Where does amino acid degradation take place and what are the two steps involved?

A

> Liver

  1. Removal of the –NH2 group (transamination, oxidative deamination and urea cycle)
  2. Degradation of the remaining carbon skeleton
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8
Q

What is transamination?

A

The transfer of the –NH2 group of an α-AA to an α-keto acid

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9
Q

What is Oxidative Deamination?

A

> amino acid converted into a keto acid with the release of an ammonium ion

i.e. glutamate loses its amino group (NH3+), with the amino group accepting additional H+ to form the ammonium ion (NH4+). Once glutamate has lost its amino group, it is now a keto acid (alpha- ketoglutarate).

> occurs in liver and kidney mitochondria

> catalyzed by the enzyme Glutamate dehydrogenase

> requires NAD+ as coenzyme, which produces NADH that in turn enters the ETC and forms ATP.

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10
Q

Urea cycle purpose

A

Urea is produced from NH4+ and aspartate

Gets rid of toxic nitrogen from the body

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11
Q

Where does the urea cycle occur?

A

The first step of the urea cycle occurs in the mitochondria, where the required enzyme is located.

Steps 2, 3 and 4 occur in the cytosol, where the required enzymes are located.

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12
Q

Where does the input required for the urea cycle come from?

A

The oxidative deamination removes the amino group from glutamate

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13
Q

What must happen to the ammonium ion before the urea cycle can begin?

A

Used to create a compound called carbamoyl phosphate

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14
Q

What is the purpose of performing an oxidative deamination reaction (shown below), as part of amino acid metabolism?

A

Oxidative deamination produces the ammonium ion (NH4+), which is incorporated into carbamoyl phosphate that is required to begin the urea cycle

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