FA Beta-Ox and FA Ox- Brar Flashcards

1
Q

What is the only FA to be considered gluconeogenic? How is it produced and what does it eventually become?

A
Propionyl CoA (from beta-ox of odd chain FA's)
End product=Succinyl CoA-->TCA-->Malate-->glucose (via gluconeogenesis)
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2
Q

For beta-ox of odd chain FAs, 3 additional enzymes are required to metabolize propionyl CoA. What cofactors are required (3)?

A

Biotin, ATP, and vitamin B12

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3
Q

What are the 3 ketone bodies? Who uses them?

A
  • Acetoacetate, acetone and 3-hydroxybutyrate

- skeletal muscle, brain, kidney, intestinal mucosa.

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4
Q

What are the 6 ketogenic AAs? What can they be broken down into?

A

-Leucine, Isoleucine, Lysine, Tryptophan, Phenylalanine and Tyrosine.
(Please let tommy in the library)
-Can be broken down into AcCoA or acetoacetyl CoA

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5
Q

What is peroxisomal Beta-Ox used for? How does it differ from mitochondrial Beta-Ox?

A
  • 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.
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6
Q

Where does long chain branched FA (alpha-Ox) take place? What is produced? What are the common LCBFAs (2)?

A
  • 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)
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7
Q

What is MCAD Deficiency? What alpha-ox pathway is upregulated?

A
  • Medium Chain Acyl CoA DH

- Phytanic Acid

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8
Q

What is omega-ox? Where does it take place? What cofactors are required?

A
  • 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.
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9
Q

How are peroxisomal alpha and beta oxidation and microsomal omega oxidation regulated?

A

Substrate availability only

NO FEEDBACK REGULATION

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