Lecture 23: FA Synthesis Flashcards
Differences between FA synth. and beta oxidation
- FAS in cytoplasm, not mito.
- Reducing equivalents come from NADPH, not FAD/NAD
- Most carbons are from malonyl-CoA, not acetyl-CoA
- Acyl-carrier protein used, not CoA
- Rxns performed by 1 large complex, not individual enzymes
Purpose of citrate pyruvate shuttle
Brings acetyl-CoA from mitochondria to cytoplasm and converts NADH into NADPH for FAS (rest from PPP)
Citrate-pyruvate cycles for 1 palmitate
8 cycles = 8 acetyl-CoA and 8 NADPH (remaining 6 from PPP) for 1 palmitate
FA elongation and desaturation
Alternating elongation/desaturation occurs in the ER to diversify from palmitic acid
FA elongation
Uses NADPH, malonyl-CoA similar to FAS but separate enzymes from FAS
FA desaturation
Creates cis double bonds; enzymes remove 2 H’s at fixed positions (C4-5, 5-6, 6-7, 9-10)
Essential FAs
Humans have no enzymes for FAs with double bonds beyond C9; linoleic and linolenic acid come from diet
TAG structure
3 FAs esterified via carboxyls with glycerol backbone hydroxyls. Neutral fats that can be solid or liquid (fat or oil)
TAG FA differences by position
1: usually saturated
2: usually unsaturated
3: sat. or unsat.
Where does TAG occur in the body?
Primarily in the liver, also adipose/muscle
Glycerol for TAG synthesis source
Glycerol-3-P comes from DHAP, or in the liver glycerol kinase phosphorylates glycerol.
TAG/FA interorgan transport
The intestine exports chylomicrons, the liver exports VLDLs. Lipoprotein Lipase hydrolyzes TAGs to FAs for uptake by target tissues.
Membrane lipid classes
- Phospholipids
- Glycolipids
- Cholesterol
Phospholipids
Main membrane lipid w/ glycerol or sphingosine backbone. FA chains at C1/C2 and different C3 groups
Glycerophospholipid degradation
Phospholipase hydrolysis of specific ester/phosphodiester bonds:
-P-lipase A1 -> R1
-P-lipase A2 -> R2
-P-lipase C -> P-head group
-P-lipase D -> head group only