BMS07-1030 AA Metabolism Flashcards

1
Q

What does an essential AA mean?

A

Its needed as a building block to make other AA

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2
Q

Can all AA be made?

A

No- out of 20 10 must be eaten

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3
Q

What’s a waste product from creatine?

A

Creatinine

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4
Q

What’s a waste product from purines/pyrimidines?

A

Uric acid

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5
Q

What is turnover?

A

Body proteins always being broken back down to AA

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6
Q

Name the 3 non-essential AA that we can make from keto acids and why are they important?

A

Alanine
Aspartate
Glutamate

Metabolism

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7
Q

Why is histidine essential?

A

For growth

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8
Q

Why is arginine essential?

A

If something goes wrong

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9
Q

What is the nitrogen balance? Why does this occur?

A

Nitrogen taken in from the diet should be equal to that excreted in various waste products

The rate of protein synthesis is equal to the rate of degradation

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10
Q

When is there a positive N balance?

A

N intake is greater such as in growth and pregnancy

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11
Q

When is there negative N balance?

A

In starvation or injury

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12
Q

How are cellular proteins removed?

A

Ubiquitin breakdown

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13
Q

What hormone can increase protein breakdown?

A

Cortisol

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14
Q

How are organelles removed?

A

Taken into vesicles which fuse with lysosomes

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15
Q

Deamination

A

AA + water + coenzyme(NADP) = keto acid + ammonia + coenzyme (NADPH)

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16
Q

What is a keto acid?

A

R-C-COOH

The middle C is double bonded to O

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17
Q

Transamination

A

AA + keto acid = keto acid 2 + AA 2

Coenzyme used

Using an aminotransferase enzyme

18
Q

Which AA is used in transamination and why?

A

Glutamate as its the only one there’s an enzyme for (glutamate dehydrogenase)

19
Q

What 2 things do AA break into?

A

Ammonia and a keto acid

20
Q

Which part of the AA is removed to get a keto acid?

21
Q

What do most AA become when loosing the amino group?

22
Q

How can keto acids be used? (2)

A

Metabolised in the TCA cycle to carbon dioxide and water to make ATP

13 of them can be converted back to glucose by the liver (glucogenic)

23
Q

What can leucine and lysine be degraded into?

A

Acetyl coenzyme A (ketogenic)

24
Q

Which 3 AA are needed for urea synthesis?

A

Aspartate
Alanine
Glutamate

25
What is alanine used to make?
Pyruvate
26
What is transdeamination and where does this occur?
A mixture of transamination and deamination Liver
27
What does the liver synthesis?
Haem Purines Pyrimidines Plasma proteins
28
Which organ convert the amino groups to urea?
Liver
29
What are ammonia groups transported as in the blood stream?
Glutamine as it has 2 amino groups so carries them efficiently
30
What happens when glutamine is converted to glutamate?
Glutaminase | Water turns to ammonia
31
What happens when glutamate is converted to glutamine?
Glutamine synthetase | ATP and ammonia go to ADP and Pi
32
Which AA are important for transporting N between organs? (4)
Glutamate Glutamine Aspartate Alanine
33
Why can ammonium ions be useful?
In the kidney for pH regulation
34
What is fumerate used for?
TCA cycle
35
In the urine cycle which AA makes urea?
Arginine
36
Which AA makes aspartate?
Citrulline
37
What AA does aspartate make?
Arginosuccinate
38
What is removed to form arginine?
Arginosuccinare has a fumerate removed
39
What converts ornithine to citruline? What forms this enzyme?
Carbamoyl phosphate loose a Pi, this is formed from carbon dioxide and ammonia and 2 ATP
40
What disease can ammonia cause?q
Cerebral oedema
41
What may cause an inability to convert ammonia to urea? (hyperammonaemia)
``` Liver failure Genetic defects (reduction in enzymes in urea cycle) ```