Ch. 17 Fatty Acid Metabolism Flashcards

(34 cards)

1
Q

Do all cells burn fatty acids?

A

No. All cells can burn glucose, but not all cells can burn fatty acids.

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2
Q

What are triacylglycerides (TAGs)?

A

long term energy storage molecules (fatty acids)

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3
Q

What is the energy stored in a TAG vs carbohydrates and why (3)?

A

TAGs store more energy than carbohydrates because they have more carbon, there is no water accompanying TAGs, and TAGs are reduced so there are more levels of oxidation to get to CO₂.
(carbohydrates are partially oxidized)

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4
Q

How is the majority of energy stored in humans?

A

Mostly fat. Humans store ~50X more energy in fat than glycogen.

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5
Q

What will fatty acids be metabolized to?

A

acetyl-CoA which will then go into the citric acid cycle.

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6
Q

What are the two ways fatty acids can be acquired?

A

Through your diet/eating and from adipose cells.

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7
Q

What is the mechanism of acquiring fatty acids from eating/diet? (7)

A
  1. ingested fats mix with bile salts to solubilize them
  2. lipases cleave FAs from glycerol backbone to produce FFAs
  3. FFAs taken up by epithelial cells in digestive system
  4. FFAs reassemble into TAGs
  5. TAGs are assembled into chylomicrons
  6. epithelial cells secrete chylomicrons into bloodstream
  7. adipose cells (storage) and muscle cells (use) have receptors that bind chylomicrons
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8
Q

What are bile salts?

A

Bile salts are amphipathic so they form micelles. Their precursor is cholesterol. They solubilize fats.

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9
Q

What are chylomicrons?

A

A phospholipid MONOlayer with a completely hydrophobic interior containing TAGs and cholesterols. A way to make TAG and cholesterol soluble.

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10
Q

What are apolipoproteins?

A

Proteins embedded in the phospholipid monolayer of chylomicrons that allow a receptor to bind to the chylomicron (“address label”)

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11
Q

What is the mechanism of acquiring fatty acids from adipose cells? (6)

A
  1. adipose cells receive signal via a receptor
  2. signal transduction cascade occurs
  3. adenylyl cyclase activates PKA which leads to activation of lipases in adipose cells
  4. active lipases produce FFAs from TAGs
  5. serum albumen binds FFAs and makes them soluble in the bloodstream
  6. cells recognize, bind, and internalize serum albumen
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12
Q

What is serum albumen?

A

A protein that binds FFAs and makes them soluble in cells.

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13
Q

Where does β-oxidation take place?

A

In the mitochondrial matrix.

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14
Q

How do FFAs get into the mitochondrial matrix to undergo metabolism?

A

It gets converted to acyl CoA and transported by an antiporter.

FFA + CoA + ATP → acyl CoA + AMP + PPᵢ

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15
Q

What does the conversion of FFA to acyl CoA cost?

A

It costs two phosphoanhydrides to “activate” FFA to acyl CoA. (energy investment)

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16
Q

Is acyl CoA soluble and where can it go?

A

It is free to diffuse through the cytosol and does. It can diffuse through the outer mito. membrane, but NOT the inner mito. membrane (no transport protein)

17
Q

How does acyl CoA get through the inner mitochondrial membrane?

A

A carnitine group is added to acyl CoA to produce acylcarnitine. Carnitine:Acylcarnitine translocase transports it across the membrane.

18
Q

What is the carnitine:acylcarnitine translocase?

A

An antiporter in the inner mito. membrane that transports acylcarnitine into the matrix while simultaneously transporting carnitine out of the matrix.

19
Q

What does the enzyme on the translocase do?

A

enzyme on the antiporter immediately cleaves carnitine off the acyl group and reattatches the FFA to CoA

20
Q

What is β-oxidation?

A

a spiral pathway of fatty acid metabolism; kind of circular but every revolution the fatty acid gets two carbons shorter

21
Q

What does each revolution of β-oxidation produce?

A

Every revolution produces acetyl-CoA, FADH₂, and NADH

22
Q

What is the β-oxidation net reaction of ONE revolution?

A

Rₙ-CoA + NAD⁺ + FAD + CoA + H₂O → acetyl-CoA + NADH + H⁺ + FADH₂ + Rₙ_₂-CoA

23
Q

How do you determine the number of revolutions a fatty acid will undergo and why?

A

of revolutions = (# of C / 2) - 1
The last revolution produces acetyl-CoA so subtract 1.

24
Q

What are the total products for β-oxidation and the citric acid cycle? (one round)

A

β-oxidation: (C/2) acetyl-CoA, (C/2)-1 NADH, and (C/2)-1 FADH₂
Citric Acid Cycle (for one acetyl-CoA): 3NADH, 1 FADH₂, and 1 GTP/ATP

25
What is the NADH and FADH₂ conversion factor for ATP?
1 NADH = 3 ATP 1 FADH₂ = 2 ATP
26
Why does fatty acid metabolism need regulation?
Acetyl-CoA can either go into the citric acid cycle (catabolism in mitochondria) or fatty acid synthesis (anabolism in cytosol).
27
What is the main regulatory mechanism for fatty acid metabolism?
Carnitine:Acylcarnitine Translocase is the main regulatory enzyme.
28
How is Carnitine:Acylcarnitine Translocase inhibited?
Inhibited my malonyl-CoA which is synthesized from acetyl-CoA. Inhibition of this enzyme means there is no feedstock for β-oxidation (literally denying substrate).
29
What else is regulated in β-oxidation (2) and how?
Two enzymes in β-oxidation are inhibited by high [NADH]/[NAD⁺] ratios. (feedback inhibition; if there is a lot of NADH you don't need more)
30
What are ketone bodies?
Something that acetyl-CoA can be converted to in the liver. There are three major ketone bodies. (NOT produced from anything other than acetyl-CoA)
31
Can all tissues use ketone bodies as fuel/energy?
No. Only some tissues can use ketone bodies as fuel.
32
Which cells can use ketone bodies (2)? Which cannot (1)?
Brain and muscle can use them. The liver CANNOT use them.
33
What is the pathway to make ketone bodies? (3)
1. two acetyl-CoA come together to produce acetoacetyl-CoA via thiolase 2. acetoacetyl-CoA and acetyl-CoA produce HMG-CoA (which is a precursor to cholesterol synthesis) 3. HMG-CoA is converted to acetoacetate (and from there can become any other ketone body)
34
Why are ketone bodies important?
The brain needs something to use if glucose runs out. Ketone bodies are what it can use.