USMLE

Fatty Acid Breakdown (Carnitine Shuttle)

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Biochemical Pathways
  1. Glycolysis
  2. Electron Transport Chain (ETC)
  3. Cori Cycle
  4. De Novo Purine Synthesis
  5. De Novo Pyrimidine Synthesis
  6. Purine Salvage
  7. Purine Excretion
  8. Ethanol Metabolism
  9. Pyruvate Metabolism
  10. HMP Shunt (Pentose Phosphate Pathway)
  11. Galactose Metabolism
  12. Sorbitol (Polyol) Pathway
  13. Urea Cycle
  14. Alanine (Cahill) Cycle
  15. Catecholamine Synthesis & Breakdown
  16. Homocysteine Metabolism
  17. Fatty Acid Synthesis (Citrate Shuttle)
  18. Fatty Acid Breakdown (Carnitine Shuttle)
  19. Propionic Acid Pathway
  20. Fructose Metabolism
  21. Regulation by Fructose-2,6-Bisphosphate (F-2,6-BP)
  22. Glycogenesis

Fatty Acid Breakdown is a biochemical pathway involving the Carnitine Shuttle, used to metabolize fatty acids into molecules that can be harnessed for energy. This process usually occurs in the liver.

The pathway begins with fatty acids and coenzyme A (CoA), which are combined to form acyl-CoA. This Acyl-CoA is then shuttled via carnitine into the mitochondrial matrix, a process that can be inhibited by high levels of malonyl-CoA.

Inside the mitochondrial matrix, acyl-CoA dehydrogenase performs beta-oxidation, converting acyl-CoA into acetyl-CoA. Acetyl-CoA is a versatile molecule used to produce ketone bodies for export, or ATP via the Kreb’s Cycle for intracellular use.

Find Fatty Acid Breakdown and more Biochemical Pathways among Pixorize's visual mnemonics for the USMLE Step 1 and NBME Shelf Exams.