FA Synthesis Flashcards
1
Q
Acetyl CoA Carboxylase consists of?
A
- biotin carboxlyase
- transcarboxylase
- Biotin-carboxyl Carrier Protein (BCCP)
2
Q
Acetyl transferred from mitochondrial pool into cytosol during fed-state by means of a malate-citrate shuttle, a process that involves?
A
- Acetyl-CoA condensing with OAA to form citrate (TCA)
- Citrate crossing mitochondrial membrane into cytosol
- Exported citrate undergoing the reverse rxn forming Acetyl-CoA & OAA, a rxn catabolised by ATP-citrate lyase
Acetyl-CoA cannot be converted into pyruvate or OAA in animals, hence animals cannot convert fat into sugars.
3
Q
FAS Synthase rxn
A
- located in cytosol
- End-product is palmitic acid C16:0
- pathway essentially same in most organisms
- FAS enzyme has phosphopantetheine-binding domain, referred to as ACP
- Before 1st condensation rxm, 2 thiol groups must be loaded.
- Acetyl CoA is transferred initially to ACP and then to thiol group of ketoacyl-ACP synthase
- Malonyl group from malonyl-CoA transferred to a thiol group of ACP.
- ACP acts as flexible arm involved in building an acyl chain by moving the substrate from one active site to the next in a sequential manner
- Condensation rxn
- Reduction
- Dehydration
- Reduction
- Butyryl-ACP (4C) then enters 2nd round of FA synthesis
- Cycle continues until palmitoyl-ACP is produced
- Thioesterase releases palmitic acid into cytosolic pool
- All C in palmitic acid derived from malonyl-CoA except 2C at methyl-end from Acetyl-CoA
4
Q
CPT-1 inhibition
A
- Malonyl-CoA has inhibitory effect on CPT-1
- prevents newly synthesized acyl-CoA from undergoing immediate Beta-oxidation
5
Q
Lactating mammary gland FA synthesis?
A
- MCFA: end-product of FA synthesis in mammary gland, usually C8:0 & C10:0
- mammary thioesterase isoforms specific to MCFA
- secreted in esterified (TAG) as milk fat
6
Q
FA Elongation rxn
A
- 2 different FA elongation pathways:
- Microsomal pathyway: uses malonyl-CoA
- Mitochondrial pathway uses Acetyl-CoA
7
Q
Desaturation of FA
A
- Desaturation of FA in animals & plants occurs by means of aerobic desaturation, whereby 2 H atoms removed from an acyl chain are subsequently used to reduce O2 to H2O via NADPH & other reductants.
- Humans have C9, 6, 5, &4 desaturases but lack enzymes to desaturate beyond delta9 position in the hydrocarbon chain.
- mammals cannot synthesize essential FA linoleate (C18:2) or alpha-linolenate (C18:3)
- mammals capable of introducing double bonds b/w delta9 position & carboxyl end of hydrocarbon chain.
- therefore, possible to desaturate oleate further at delta6 position, forming an C18:2 delta6,9 FA
- All desaturases associated with microsomes
- Stearoyl-CoA (C18:0) can be desaturated to form oleoyl-CoA (C18:1delta9) by means of a complex rxn involving the following microsomal enzymes
- requires delta9 desaturase to make stearic acid
- Stearoyl-CoA desaturase cytochrome b5 reductase
*
8
Q
Essential FA (EFA) families
A
- EFA are either membres of n-3 or n6 families
- n-3 families
- alpha-linolenic C18:3delta9,12,15
- EPA C20:5
- DHA C22:6
- n-6 family
- Linoleic acid (18:2delta9,12)
- gamma-Linolenic (18:3delta6,9,12)
- Arachidonic acid (20:4delta5,8,11,14)
9
Q
Mead acid
A
- Redundant eicosanoids
- biomarker for EFA deficiency
- when the body is deficient in EFAs. it responds by trying to synthesize “next best thing”, i.e. Mead acid, C20:3
10
Q
DHA C22:6 is a key PUFA in brain tissue
A
- Not all PUFAs are equally converted to VLCFAs because of the limiting activities of some of the enzymes (i.e. elongase, delta5 & delta6 desaturase)
- humans rely on exogenous sources of EPA & DHA in their diet to supplement the endogenously synthesized FA
11
Q
Regulation of FA synthesis
A
- Acetyl CoA Carboxylase key regulatory enzymes
- short-term
- Citrtate activates
- Palmitoyl-CoA inhibits
- Insulin stimulates phosphatase to activate
- Glucagon/Epi stimulates PKA to inactivate
- Long-term
- high carb diet increases expression of Acetyl-CoA Carboxylase (& FAS)
- short-term