Chapter 27 Fatty Acid Degradation
What does muscle weakness and cramping affecting skeletal muscle, heart, and kidney likely
indicate?
carnitine excess in the diet
loss of hormone-sensitive lipase activity
malfunctioning or deficient carnitine translocase
Three rounds of fatty acid oxidation result in
two acetyl CoA molecules.
three acetyl CoA molecules.
the synthesis of palmitate.
the formation of enoyl CoA.
the complete oxidation of palmitate B.
The activation of fatty acids for degradation takes place in two steps. What is the intermediate
formed and why is activation necessary for β oxidation to occur?
Acyl adenlyate; the cAMP formed by this reaction activates protein kinase A.
Acyl adenlyate; only the activated form of the fatty acid can react with coenzyme A.
Propionate; only the activated form of the fatty acid can react with coenzyme A.
Acyl carnitine; the cAMP formed by this reaction activates protein kinase A.
Acyl carnitine: this intermediate is needed to fuel the carnitine cycle.
Exercising first thing in the morning without eating mobilizes lipid stores for fuel. All of the
below are involved in this mobilization, EXCEPT
glucagon binds 7TM receptors that activate adenylate cyclase.
perilipin is phosphorylated.
cAMP stimulates protein kinase A.
hormone-sensitive lipase completes the mobilization of fatty acids with the production of
a free fatty acid and glycerol.
hormone-sensitive lipase is phosphorylated.
What is the role of acetoacetate in lipid metabolism in addition to providing energy when blood
glucose is low?
Acetoacetate is used to synthesize glucose when glucose stores are low.
Acetoacetate can be readily converted to oxaloacetate, a precursor for the amino acid
aspartate.
Acetoacetate has a pKa near 7.4 and so it can act as a blood buffer when glucose is low.
Acetoacetate can be converted to lactate and so it can provide energy in the same way that
is done under anaerobic glycoliysis.
The liver lacks CoA transferase and so it releases acetoacetate into the blood for us by
other tissues.
Ans: C Section: 27.1