Fatty Acid Catabolism & The Citric Acid Cycle Flashcards

1
Q

Which ONE of the following is the major storage form of fats?

A) Phospholipid
B) Cholesterol
C) Arachidonic Acid
D) Triacylglycerol
E) Laminin

A

D) Triacylglycerol

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2
Q

Which ONE of the following biomolecules restricts untimely access to triacylglycerol mobilisation from adipocytes?

A) Glycerol
B) Perilipin
C) Lipoprotein
D) Serum Albumen
E) Diacylglycerol

A

B) Perilipin

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3
Q

Which ONE of the following enzyme types when activated mobilises triacylglycerols?

A) Catalase
B) Synthase
C) Dehydrogenase
D) Lipase
E) Hydratase

A

D) Lipase

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4
Q

Beta-oxidation occurs in which ONE of the following cellular locations?

A) Cytosol
B) Golgi
C) Mitochondria
D) Nucleus
E) Plasma Membrane

A

C) Mitochondria

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5
Q

Which ONE of the following binds fatty acids in the bloodstream after they are released from adipocytes?

A) Serum Albumen
B) Glucose
C) Acetyl-CoA
D) Cholesterol
E) Glycogen

A

A) Serum Albumen

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6
Q

Which ONE of the following enzymes activates a fatty acid to a fatty acyl-CoA?

A) Acyl-CoA Kinase
B) Acyl-CoA Phosphotase
C) Acyl-CoA Dehydrogenase
D) Acetyl-CoA Synthetase
E) Acyl-CoA Carboxylase

A

D) Acetyl-CoA Synthetase

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7
Q

Which ONE of the following is the major regulatory enzyme in fatty acid catabolism?

A) Carnitine Acyl-Transferase-1
B) Acyl-CoA Dehydratase
C) Acyl-Phosphotase
D) Phosphofructokinase
E) Pyruvate Kinase

A

A) Carnitine Acyl-Transferase-1

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8
Q

A 20 carbon fatty acyl-CoA will degrade to which one of the following number of Acetyl-CoA?

A) 8
B) 8
C) 12
D) 11
E) 10

A

E) 10

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9
Q

How many of the following NADH and FADH2 are formed when a 16 carbon fatty acid undergoes complete beta-oxidation?

A) 6 NADH and 7 FADH2
B) 8 NADH and 8 FADH2
C) 12 NADH and 10 FADH2
D) 7 NADH and 7 FADH2
E) None of the above

A

D) 7 NADH and 7 FADH2

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10
Q

Which ONE of the following enzymes in beta-oxidation can malfunction due to an inherited genetic mutation that is tested for at birth?

A) Acyl-CoA Dehydrogenase
B) Acyl-CoA Kinase
C) Acyl-CoA Hydratase
D) Acyl-CoA Phosphatase
E) Acetyl-CoA Synthetase

A

A) Acyl-CoA Dehydrogenase

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11
Q

Where are fatty acids stored in higher vertebrates?

A

Stored at Triacylglycerols in Adipocytes

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12
Q

What type of bond is involved in joining fatty acids to the glycerol backbone in TAGs?

A

Ester bonds

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13
Q

What tissues use a lot of fatty acids for energy?

A
  • Liver
  • Heart
  • Resting skeletal muscle
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14
Q

Are fatty acids more or less reduced than glucose?

A

More reduced and less hydrated

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15
Q

Why are TAGs a better storage form of energy than glycogen?

A

More reduced and less hydrated so can stockpile large quantities in adipocytes

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16
Q

What enzymes cause the mobilisation of fatty acids from adipocytes?

A

Lipases

Hydrolyse ester linkages

17
Q

Describe how fatty acids are mobilised from adipocytes

A
  • Adrenaline & Glucagon secreted in response to low blood sugar, and PKA activated
  • PKA phosphorylates perilipins to open lipid droplet
18
Q

What do Triacylglycerol lipases do?

A

Degrade TAGs to liberate fatty acids

19
Q

What does fatty acid activation involve?

A

The adding of CoA on to fatty acid by Fatty Acyl-CoA Synthetase

20
Q

What transport system brings fatty acyls into mitochondria?
(Describe it)

A
  • Fatty acyl-CoA bond hydrolysed by carnitine acyl-transferase-1 & fatty acid group attaches to -OH of carnitine
  • Fatty acyl-carnitine enters mitochondrial matrix through carnitine transporter
  • Fatty acyl group enzymatically transferred ito intramitochondrial CoA by carnitine acyl-transferase-2
21
Q

Describe the FOUR enzyme steps of Beta-Oxidation

A
  1. Dehydrogenase - removes 2H+ to FAD to FADH2
  2. Hydratase - H20 added
  3. Dehydrogenase - removes 2H+ to NAD+ to NADH + H+
  4. Thiolase - entry of CoA-SH to form Acetyl CoA

Each 2C of fatty acyl-CoA cleaved & converted to Acetyl-CoA

22
Q

How many FADs and NADs are reduced in the oxidation of 16C palmitoyl-CoA?

A

7 FADs & 7 NADs

23
Q

How many acetyl-CoAs are made from the degredation/oxidation of 16C palmitoyl-CoA?

A

8

24
Q

What is the outcome of genetic defects in Acyl-CoA dehydrogenase?

A
  • low energy
  • fat accumulation
  • vomiting
  • sleeplessness
  • coma
25
Q

What is the major enzyme that controls fatty acid catabolism?

A

Acyl-CoA Dehydrogenase

26
Q

What are ketone bodies?

A

Alternative energy source used when glucose is not readily available

27
Q

What are the THREE ketone bodies?

A
  1. Acetone
  2. Acetoacetate
  3. D-𝛽-Hydroxybutyrate
28
Q

Where are ketone bodies made mostly in the body?

A

Liver

29
Q

When does ketone body formation happen?

A

When carbohydrates are unavailable
* low carb diet
* starvation
* fasting
* untreated diabetes

30
Q

How do ketone bodies give energy?

A
  • Acetyl CoA from 𝛽-oxidation can’t enter citric acid cycle so are converted to ketone bodies
  • Exported as energy source to tissues that need it
31
Q

Is overproduction of ketone bodies dangerous?
Explain

A

Yes.
Blood pH decreases β€”> acidosis β€”> ketosis β€”> coma