Chapter 16: Problem 5
What causes ketoacidosis, and what are its symptoms?
Chapter 16: Problem 5
What causes ketoacidosis, and what are its symptoms?
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Get started for freeDescribe the pathway by which excess acetyl-CoA produced by the pyruvate dehydrogenase reaction in the mitochondrial matrix of liver cells is used to synthesize triacylglycerols that are exported into the blood as VLDL particles. Specifically, what key enzymes are required, and how is flux through this carbohydrate \(\rightarrow\) lipid pathway maintained under conditions of high energy charge?
Why do fatty acids destined for degradation in the mitochondrial matrix need to first be activated by linkage to coenzyme \(A\); that is, what purpose does it serve?
What are the four types of chemical reactions needed in the mitochondrial \(\beta\) -oxidation pathway to remove a \(\mathrm{C}_{2}\) acetyl group in the form of acetyl-CoA? Include the names of the mitochondrial enzymes that catalyze each reaction.
Sphingomyelin contains a phosphate in its head group, so is it a phospholipid or a sphingolipid? Where does the phosphate group come from in sphingomyelin?
Compare and contrast the fatty acid degradation and fatty acid synthesis pathways in eukaryotic cells.
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