Oxidation of Amino acids and fatty acids Flashcards

(31 cards)

1
Q

What are Fatty acids an important source of?

A

energy in many organisms and tissues

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2
Q

What is produced during the oxidation of Fatty acids? What can this be used for?

A

Acetyl-Coenzyme A
-can be used to generate energy via various pathways

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3
Q

What is the mechanism of the conversion of Fatty Acids to Acetyl CoA?

A

B-oxidation

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4
Q

What does the binding of glucagon to a receptor due to low levels of glucose do?

A

-causes free FAs to leave the adipocyte, travelling through the blood to provide energy to cells

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5
Q

Where does 95% of biologically available energy of triglycerides reside?

A

Fatty Acids

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6
Q

Once released by_____, the glycerol is processed via_____

A

lipase, glycolysis

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7
Q

What can be used to synthesise membrane lipids?
What can also occur?

A

Fatty acyl coA esters
-also transported into the mitochondrion and oxidised to produce ATP.

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8
Q

What is the first stage of Fatty Acid Oxidation?

A

Long-chain fatty acids oxidised to give Acetyl-CoA (B oxidation)

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9
Q

What is the second stage of Fatty Acid Oxidation?

A

Acetyl groups oxidised to C02 via citric acid cycle

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10
Q

What is Stage 3?

A

Electrons from stages 1 and 2 pass to 02 via respiratory chain, generating ATP

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11
Q

How many steps are there in B-oxidation?

A

4

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12
Q

What happens for each fatty acid?

A

these are repeated until the final reaction leaves acetyl-CoA (when starting with an even number of Carbons)

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13
Q

When are additional enzyme steps required?

A

if the fatty acid is:
-unsaturated
-has an odd number of carbons

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14
Q

What can have series consequences given that stored triacylglycerols are the chief source of energy?

A

inability to oxidise fatty acids

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15
Q

What is the most common genetic defect?

A

in US and Northern Europe
-mutation in the gene encoding medium-chain acyl-CoA dehydrogenase (MCAD)

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16
Q

What are the consequences of this?

A

mortality from the disease is 25-60%

17
Q

What can be done to counter if recognised early?

A

infants can be fed low-fat, high carbohydrate diet

18
Q

What does B-oxidation essentially do?

A

uses 4 reactions to remove each Acetyl-CoA

19
Q

What do stages 2 and 3 involve?

A

citric acid cycle and respiratory chain–> significant amounts of ATP generated

20
Q

How many additional enzymes are required if an odd number of FAs are present?

A

3 additional enzymes

21
Q

What does Oxidative degeneration of amino acids generate?

A

significant amounts of metabolic energy

22
Q

What are the 3 circumstances in which amino acid oxidation occurs?

A

-normal synthesis and degradation of cellular proteins
-when ingested amino acids exceed the needs for protein synthesis
-during starvation when carbohydrates unavailable or uncontrolled diabetes

23
Q

What is an important feature of amino acid degradation?

A

to separate the a-amino group from the carbon skeleton

24
Q

Where are amino acids catabolised?

A

in vertebrate liver

25
What occurs if muscle metabolises amino acids?
nitrogen is transferred to alanine, then released into the bloodstream--> then converted to pyruvate in the liver
26
How is excess nitrogen excreted?
via the urea cycle
27
How are amino acids grouped?
according to end product degeneration (glycogenic and ketogenic)
28
What are ketogenic diets restricted in?
carbohydrates and promoted as good for weight loss
29
When are ketone bodies only significant fuels?
only with adequate fat mass--> upon complete depletion of fat amino acids are mostly converted to glucose (B)
30
When an enzyme in a metabolic pathway is defective, what usually occurs?
the substrate can build up to toxic levels
31
Carbon skeletons undergo_______ to compounds that can be converted to_____ and _____
oxidation, glucose, ketone bodies