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Compare fats and sugars as energy sources.
Fats: long-term storage, slow delivery, more energy per carbon (more reduced), less water.
Sugars: short-term energy, quick delivery, stored as glycogen.
How are fatty acids absorbed and transported?
Emulsified by bile salts in the intestine → packaged into chylomicrons → travel in blood.
Free fatty acids bind to albumin for transport to tissues.
How are fats stored in the body?
Stored in adipocytes: white fat (energy), brown fat (heat generation), beige fat (derived from white fat).
What is lipolysis and how is it regulated?
Lipolysis: breakdown of triacylglycerols into free fatty acids + glycerol.
Activated by glucagon and epinephrine, inhibited by insulin.
Where do the components of triacylglycerol go after breakdown?
Glycerol → glycolysis or gluconeogenesis; fatty acids → β-oxidation for energy.
How are fatty acids transported through the body?
Bind to albumin for circulation and delivery to tissues.
Describe the carnitine shuttle.
Long-chain fatty acids converted to acyl-CoA → transferred to carnitine via CAT I → transported into mitochondria → converted back to acyl-CoA by CAT II.
List and describe the steps of β-oxidation.
1. Dehydrogenation (FADH2 produced)
2. Hydration (adds OH)
3. Dehydrogenation (NADH produced)
4. Thiolysis (releases acetyl-CoA, shortens chain by 2C).
What is the role of the trifunctional protein (TFP)?
Processes long-chain fatty acids (≥12C); catalyzes hydration, dehydrogenation, and thiolysis; facilitates substrate channeling.
What is the ATP yield of one palmitate molecule (C16)?
8 acetyl-CoA, 7 NADH, 7 FADH2 → total ~108 ATP after full oxidation.
How does β-oxidation differ for unsaturated fatty acids?
Requires an isomerase to convert cis → trans double bonds; polyunsaturated fats also require a reductase.
How does β-oxidation differ for odd-numbered fatty acids?
Produces propionyl-CoA → converted to succinyl-CoA (enters citric acid cycle).
What is the role of coenzyme B12 in fatty acid metabolism?
Vitamin B12 (cobalamin) is required for conversion of propionyl-CoA to succinyl-CoA; deficiency causes pernicious anemia.
How do insulin and glucagon regulate fatty acid metabolism?
Insulin (high energy): activates synthesis (dephosphorylates ACC).
Glucagon (low energy): activates breakdown (phosphorylates ACC).
Where does β-oxidation occur in animals and plants?
Animals: mitochondria (ATP generation).
Plants: peroxisomes/glyoxysomes (heat production).
When and where are ketone bodies formed?
Formed in the liver during low glucose (fasting, starvation, diabetes) when acetyl-CoA accumulates.
Why are ketone bodies important for the brain?
The brain cannot use fatty acids; during glucose shortage, it uses ketone bodies
(acetoacetate, β-hydroxybutyrate) for energy.
What happens if ketone levels become too high?
Excess ketone bodies lower blood pH, causing ketoacidosis; high acetone gives fruity breath odor.