Fatty Acid Synthesis Flashcards

1
Q

De novo synthesis mostly occurs where in the body

Where in the cell?

A

Liver, lactating mammary glands and some in adipose

Cytosol

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2
Q

What is the rate limiting and regulated step for fatty acid synthesis?

Why is this important?

A

Carboxylation (adding carbon) of acetyl CoA to form malonyl CoA

Because malonyl CoA is the precursor for fatty acid synthesis

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3
Q

Short term regulation of ACC is done by?

A

Protein kinase A and protein phosphatase

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4
Q

Long term regulation of ACC is done by

A

Prolonged high calorie and high carb diet will increase ACC (increase fatty acid synthesis)

Prolonged low calorie or high fat diet will decrease ACC (reduces fatty acid synthesis)

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5
Q

Once final fatty acid length is 16 carbons, there will be termination in synthesis with end product ___

What happens to this end product

A

Palmitoyl-S-ACP

Palmitoyl thioesterase cleaves the thioester bond releasing saturated palmitate (16:0)

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6
Q

Two sources of NADPH

A

HMP shunt (mostly) and malate oxidation and decarboxylation by malic enzyme (one of first steps in handwritten note)

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7
Q

Palmitate (16:0) is further elongated where?

Very long chain FAs need to be generated for?

A

Smooth ER

Brain lipids

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8
Q

Structure of triacylglycerol (TAG)

A

Carbons of glycerol:
Carbon 1: saturated FA of varied length (often 16)
Carbon 2: unsaturated FA of varied length
Carbon 3: saturated or unsaturated FA of varied length

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9
Q

3 qualities of TAG that come into play for its storage?

A
  1. Only slightly soluble in water
  2. Unable to form micelles independently
  3. Able to coalesce (form oil droplets)
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10
Q

Synthesis of TAG requires production of the following 2 TAG building blocks

A
  1. Glycerol phosphate (initial acceptor of activated FAs during TAG synthesis)
  2. Acyl CoA (FFAs must be converted to activated form)
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11
Q

Glycerol Phosphate:

  1. Two places where it is produced
  2. Two pathways in which it is produced
A
  1. Liver and adipose
  2. Glycolytic pathway (glucose-> DHAP by glycerol phosphate dehydrogenase) and
    Free glycerol -> glycerol phosphate by glycerol kinase (in liver only)
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12
Q

When will no TAG production occur?

A

When plasma glucose and insulin levels are low (because GLUT4 for adipose is insulin dependent - so adipose will not be able to synthesize glycerol phosphate without insulin)

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13
Q

Converting FFA to acyl CoA is catalyzed by ?

A

Thiokinase

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14
Q

4 reactions required to assemble TAG from glycerol phosphate and fatty acyl CoA

A
  1. Sequential addition of 2 FAs from fatty acyl CoA to glycerol phosphate (by acyltransferase)
  2. Removal of phosphate group by a phosphatase
  3. Addition of a third FA by an acyltransferase
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15
Q

How is TAG stored in adipose tissue?

Why?

A

As cytosolic lipid droplets.

FAs from TAG in this format are easily mobilized when fuel is required

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16
Q

~small amount of TAG are stored in liver

  1. How are they packaged?
  2. Function of VLDL
A
  1. With other lipids and apoproteins to form VLDLs

2. Secreted to blood and deliver endogenously synthesized lipids to peripheral tissues

17
Q

Difference between chylomicrons and VLDLs?

A

Chylomicrons deliver exogenous dietary acquired lipids (and TAG); VLDLs deliver de novo synthesized lipids