W6 A Protein Metabolism Amino Acids (AA) Flashcards

1
Q
  • How do dietary proteins get digested in Amino Acids?

give the organ where is occurs and what helps with digestion

A
Stomach (proteins to polypeptides)
- HCL
- Pepsin
Pancreas 
- Peptidases 
Small intestine (polypeptides to amino acids)
- Peptidases
-  Absorbed as amino acids
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2
Q
  • How many AA do we have in the body?

- What are AA comprised of?

A
  • We have 20 AA in the human protein

- Carbon, Hydrogen, Oxygen, Nitrogen (amino group) and R group (specific)

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3
Q

AA Fed State:

- What happens to AA whilst the body is in the fed state?

A
  • AA arrive at the liver via hepatic ported vein

- Then protein synthesis occurs, transported to other tissues (muscles, membranes) and its stored (TAG)

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4
Q

AA Fasted State:

- What happens to AA whilst the body is in a fasted state?

A
  • The body needs to make energy

- It breaks down AA (Muscles functional proteins & Carbon skeleton)

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5
Q
Alpha Keto (a-Keto) Acids:
- What is the difference between AA and a-Keto acids?
A
  • They are not comprised of the same materials (they are similar but not the same)
  • AA have NH2 and an extra H whereas, a-Keto acids only have an extra O.
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6
Q
  • What are Alpha Keto (a-Keto) Acids comprised of?

- What cycle do these feed into?

A
  • Carbon
  • Hydrogen
  • Oxygen
  • R group (specific)
    These feed into the TCA cycle
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7
Q
  • What’s the most common way to remove N from AA?
A
  • Transaminate the AA with an a-Keto acid and move N from AA to a-Keto.
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8
Q
  • What is deamination through dehydrogenase?
A
  • When AA and a-Keto acids remove N
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9
Q
  • What is the definition of transamination?
  • Are transamination reactions freely reversible?
  • What tissues does it occur in?
A
  • It is the transfer of an amino group from AA to an a-keto acid in the presence of a transaminase.
  • Transamination is a freely reversible reaction depending on substrate availability
  • Transamination occurs in most tissues especially muscles.
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10
Q

Name the three main transamination reactions:

A
  1. Alanine - pyruvate
  2. Aspartate - oxaloacetate
  3. Glutamate - Alpha Keto glutrate
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11
Q
  • What is oxidative deamination?
A
  • The removal of ammonia group
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12
Q

Glutamine Synthase:

- What do you make glutamine from?

A
  • Glutamine made from glutamate
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13
Q

Glutamine Synthase:

- Glutamine is a great fuel for…

A
  • GI tract & immune system
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14
Q

Nitrogen Excretion:

- What state does the body have to be in to produce a lot of ammonia?

A
  • The body produces a lot of ammonia whilst in a catabolic state because we remove nitrogen (ammonia) during exercise
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15
Q

The Urea Cycle:

What are some key points of the urea cycle?

A
  • This cycle is an irreversible reaction
  • Aspartate enters (AA) and bring nitrogen
  • An increase in AA will increase the urea out
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16
Q
  • What are branched chain AA or BCAA?
A
  • They have a branched structure

- They can only be oxidised in skeletal muscle in the mitochondria

17
Q

What are three key branched chain AA or BCAA?

A
  1. Leucine
  2. Isoleucine
  3. Valine
18
Q
  • The important AA Alanine has a one main role, what is it?

- Where is Alanine taken up by and released from?

A
  • Important for inter tissue transfer

- It is taken up by the liver and released from the muscles

19
Q

Why is the Alanine Cycle important?

A
  • It’s important because transfers glucose to the necessary tissues.
  • It also maintains glucose levels in the blood & liver.