FA Beta-Ox and FA Ox- Brar Flashcards
What is the only FA to be considered gluconeogenic? How is it produced and what does it eventually become?
Propionyl CoA (from beta-ox of odd chain FA's) End product=Succinyl CoA-->TCA-->Malate-->glucose (via gluconeogenesis)
For beta-ox of odd chain FAs, 3 additional enzymes are required to metabolize propionyl CoA. What cofactors are required (3)?
Biotin, ATP, and vitamin B12
What are the 3 ketone bodies? Who uses them?
- Acetoacetate, acetone and 3-hydroxybutyrate
- skeletal muscle, brain, kidney, intestinal mucosa.
What are the 6 ketogenic AAs? What can they be broken down into?
-Leucine, Isoleucine, Lysine, Tryptophan, Phenylalanine and Tyrosine.
(Please let tommy in the library)
-Can be broken down into AcCoA or acetoacetyl CoA
What is peroxisomal Beta-Ox used for? How does it differ from mitochondrial Beta-Ox?
- Exclusive site of very long chain FA oxidation (24-26 carbon)
- the long chain FA acyl CoA synthetase in the peroxisomal membrane DOES NOT require carnitine to translocate acyl CoA derivatives across the membrane.
Where does long chain branched FA (alpha-Ox) take place? What is produced? What are the common LCBFAs (2)?
- Oxidized in peroxisomes to a 8 carbon branched FA which is then degraded further in the mitochondria.
- Pytanic acid and pristanic acid (Breakdown products of chlorophyll, consumed through green vegetables, NOT found in animals)
What is MCAD Deficiency? What alpha-ox pathway is upregulated?
- Medium Chain Acyl CoA DH
- Phytanic Acid
What is omega-ox? Where does it take place? What cofactors are required?
- Fatty acids are oxidized at omega end by endoplasmic reticulum enzymes.
- Process utilizes cytochrome P450, molecular oxygen and NADPH to oxidize the omega carbon to an alcohol.
How are peroxisomal alpha and beta oxidation and microsomal omega oxidation regulated?
Substrate availability only
NO FEEDBACK REGULATION