CELL Lipid Synthesis and Degradation Flashcards

1
Q

Fats play an essential role in many biological functions

4 roles?

A

Fats play an essential role in many biological functions including:
• Membranes
• Important in uptake of fat-soluble vitamins
• Used as precursors for steroid hormones
• As an energy store

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Why is Fat is such an important store of energy?

A

Fat is such an important store of energy because the energy content of fat per gram is over twice that of either carbohydrate or protein. So, fat is a very good way of storing energy.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

There are major health implications of fat:

A
  • 40% of the energy of the British Diet is from fat.
  • In 2010 62.8% of adults (16+) were overweight or obese. 30.3% of children (2-15) were overweight or obese.
  • A massive 26.1% of all adults and 16% of children were obese.

This has huge costs on the NHS and results in many premature deaths every year.

The culprits of these problems are:

  • Fatty acids
  • Triglycerides or Neutral Fats
  • Cholesterol
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Fatty Acid Synthesis

when do we store fat?
what used fats as preferred source of energy?
what is msotly used for energy?
where is fat mostly stored? where is it mostly synthesised?

A

When calorific intake usually in form of carbs exceeds consumption, excess is laid down as fat. This is because we are derived as hunter-gatherers, the body is designed for periods of famine.

  • Some tissues such as cardiac muscle use fats as their preferred energy source.
  • However, dietary carbohydrate is the most common source, although amino acids can also be used.
  • Fats are stored in the adipose tissue as triglycerides but the majority are synthesised in the liver
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Lipid Synthesis and Degradation

where does synthesis and degradtion take placr? where does synthesis occur? degradation?

A

Most of the lipid synthesis and degradation occurs in the liver hepatocytes, with synthesis occurring in the cytosol and the breakdown (through beta oxidation) mostly occurring in the mitochondria.

o These reactions are largely reciprocally regulated, you get synthesis when there is excess calorie intake and during this breakdown is inhibited.
o If you need breakdown then the reactions leading to synthesis are inhibited.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what are triglycerides

structure?
why is the glycerol key?

A
  • Triglycerides are neutral fats, they consist of three fatty acids attached to a glycerol backbone.
  • Triglycerides are concentrated stores of energy.
  • Remember that the glycerol can be made from glycolysis by glycerol-3-phosphate, glycerol can also be fed into glycolysis at this point.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are fatty acids?

structure?
saturation?

example of 2 important ones?

what are essential fatty acids?

A
  • Fatty acids are chains of methyl groups with a carboxyl group at the end (terminal).
  • The fatty acids can be saturated with single bonds or unsaturated with double bonds.
  • An example of two important ones are palmitate and oleate.
  • Humans are unable to create double bonds in positions less than position nine, so fatty acids that have these are essential fatty acids and we must obtain them from out diet
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Making Fatty Acids

what is the starting block?
what would normally happen in a cell that wanted to make atp this way?

what happens in hepatocyte? what is trnasported out of where? what is this used for?

4 fates of fatty acids in the liver?

where does fatty acid synthesis occur? what 3 things is required and where do they come from?

what is a simple way of lookimf at fatty acid synthesis?

where does the NADPH come from? (2)

A

The starting block for fatty acid synthesis is Acetyl-CoA.
• If in a cell that wanted to generate ATP, the Acetyl-CoA would feed into the Krebs cycle and react with oxaloacetate to form citrate and go on to result in the ETC.

However, in a hepatocyte this isn’t generally how they make their energy, instead they make fatty acids. The following occurs:

  1. The citrate made is transported out of the mitochondria and remove the Acetyl-CoA
  2. The Acetyl-CoA then used to build up fatty acids
  3. These fatty acids can either remain in the liver (liver lipids) or be exported bound within lipoproteins or bound to albumin as free fatty acids
  4. Alternatively, the Acetyl-CoA can be used to make cholesterol, cholesterol is then transported to various tissues to be incorporated into membranes or for steroid synthesis

So, fatty acid synthesis occurs in the cytosol and requires:
• Acetyl-CoA
• NADPH (from pentose phosphate pathway)
• ATP
Fatty acid synthesis involves the sequential addition of 2 two-carbon units derived from Acetyl-CoA.

Citrate malate shuttle provides 40% NADPH needed for fatty acid synthesis 60% comes from the pentose phosphate pathway

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Transfer of acetyl-CoA to cytosol

why must there be a transfer? from where to where? what is used for this transport?

why is the process cyclical?

how does the transport occur? so what is transported out? what is this broken down into? what happens to one of these and what is it converted into? what is produced in this conversion? what happens now and how does this allow krebs cycle to continue?

first step of fatty acid synthesis - what is the enzyme? equation?

what is special about this reaction? (2) what drives it?
what inhibits this reaction?

what does acetyl-coa bind to, to allow the reaction to occur?

what 2 other things does the reaction require to occur?

A

Synthesis occurs in the cytosol, but the formation of citrate initially occurs in the mitochondria. So there needs to be transport of this citrate into the cytosol and this is done by the citrate-malate antiport.

The process is cyclical, because if you removed the mitochondria of all its citrate you would be removing a big component of the Krebs cycle because we are removing oxaloacetate essentially, as it is a cycle.

  1. The citrate is pumped out into the cytosol and breaks down to give us the Acetyl-CoA and oxaloacetate.
  2. The oxaloacetate can then be converted to malate which can be converted to pyruvate, importantly in that conversion we produce NADPH (used for FA synthesis).
  3. The pyruvate is then transported back into the mitochondrion, converted back into oxaloacetate.

The first step in fatty acid synthesis is the rate-limiting step, the enzyme that is involved in this is Acetyl-CoA (x) carboxylase.

Acetyl-CoA + ATP + HCO3- —> malonyl-CoA + ADP + Pi
2c 3c

Via acetyl-CoA carboxylase

The reaction is an important irreversible regulatory step and is driven in part by the amount of citrate that is present = positive feedback.

This makes sense as the amount of citrate in a cell will rise when the flow of glucose through glycolytic pathway is increased.
• The reaction is inhibited by palmitate (negative feedback), which is the end product of fatty acid synthesis.

Note that the Acetyl-CoA binds to a molecule that allows the reaction to occur, this molecule is acyl carrier protein (ACP).

The reaction requires the vitamin biotin to work. The reaction requires ATP.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Acetyl-CoA carboxylase
inhibition and stimulation

what inhibits the enzyme? what stimuates this process hence inhibits the enzyme?

what nutrients ratio will increase or decrease the expression of the enzyme?

A

Acetyl-CoA carboxylase is inhibited by phosphorylation. Glucagon stimulates phosphorylation and therefore inhibits the enzyme.

Expression of Acetyl-CoA carboxylase is increased by high carbohydrate and low fat.

Expression of Acetyl-CoA carboxylase is decreased by low carbohydrate and high fat.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Fatty acid synthase - importnace

what do all the enzymes required for fatty acid synthesis form? how does it exist?

what is the benefit of this?

what happens with the enzyme as the chain is increased?

what is the importance of intermediates being covalently linked to acyl carrier protein (ACP)? (2)

A

All the enzymes required for the reactions above form a multi-functional complex called Fatty acid synthase, which exists as a dimer.

• By having a multi-enzyme complex all the reactions to occur are very close to each other and the products of one reaction are very close to the active site of the next enzyme in the chain.

As the fatty acid chain is increased as the enzyme goes around and around in the cycle until the chain reaches the required length and is released.

Importance of intermediates being covalently linked to acyl carrier protein (ACP) is that this enables the efficient and rapid movement of the growing fatty acid chain to be passed from one active site to the next.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Fatty acid synthesis summary

A

takes place in the fed state when glucose levels are high and demand for ATP is low

Stimulated by insulin

Inhibited by glucagon, adrenalin and noradrenalin

Takes place in a number of tissues but primarily in the liver

Triglycerides are the major storage molecule and is composed of glycerol and free fatty acids

Stored by adipocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Cholesterol

what is this? how does it interact with water?
what is it a precursor for? (3)
what else is it used for?
what is it not used for?

how is cholesterol transported in circulation?

A
  • Cholesterol is a rigid hydrophobic molecule that is virtually insoluble in water.
  • It is the precursor of sterols, steroids and bile salts.
  • It is also an important membrane component.
  • It is not an energy-forming molecule.

Cholesterol is transported in the circulation as cholesteryl esters and as mentioned above, cannot be oxidised to O2 and H2O so can provide no energy.

Cholesterol imbalance can lead to significant health issues.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Cholesterol synthesis

where is it synthesised?
how does this process start?

what is a major regulatory step? what enzyme is used? what inhibits this enzyme?

why is it diffcult to reduce circulating cholesterol by diet alone?

A
  • Cholesterol is synthesised mostly in the ER
  • There are over 30 steps
  • Starts with the activation of acetate to acetyl-CoA.
  • So, you can generate cholesterol from a carbohydrate source, like you can generate fatty acids.
  • A major regulatory step is the conversion of 3-hydroxyl-3-methylglutaryl CoA (HMGCoA) to mevalonate by HMGCoA reductase.
  • Cholesterol inhibits HMGCoA reductase, the enzyme involved in its own synthesis

Therefore, difficult to reduce circulating cholesterol by diet alone as endogenous synthesis is increased. So, you need to tackle it by inhibiting this enzyme and diet.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Fatty Acid Degradation

where are fats synthesised in the liver transported to? how is this done? (2)

how is the fatty acid stored?

what is the first stage in degradation? where does it go after this and what happens here?

A

Fats synthesised in the liver are transported to the peripheral tissue e.g. adipocytes for storage and this is partly through binding to albumin and partly as lipoproteins.

So, the fatty acid is stored in adipocytes and then the first step then in degradation is mobilising the fatty acid in the adipocyte.

It then gets transported back to the liver and in the cytosol of hepatocytes gets activated.

Then it undergoes degradation in the liver mitochondria, the process is called beta oxidation.

So, the three steps are:

  • Step 1: Mobilisation in adipocyte
  • Step 2: Activation in hepatocyte cytosol
  • Step 3: Degradation in hepatocyte mitochondria
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Mobilisation

what is the common route for this? what does it generate? what does this activate and what does this do?
what is this responsible for?

what is acted upon and by what to produce free glycerol and free fatty acids?

A

A common route for mobilisation of fatty acids is stimulation of the 7TMD GPCR, which generates cAMP.

  1. cAMP activates PKA
  2. PKA phosphorylates triacylglycerol lipase, the enzyme responsible for the breakdown of triacylglycerol to diacylglycerol
  3. Diacylglycerol can then be further acted upon by lipases which ultimately lead to free glycerol and free fatty acids. Allowing it to be transported back to the liver.
17
Q

Activation (liver)
fatty acid degradation

what are they activated by? what do they become?

what happens to this? what is it bound to? what enzyme is required for this?

what happens now?

A

Going back to stages of degradation, the fatty acids are then transported to the liver and activated by acyl-CoA synthase in the cytoplasm to from acyl-CoA.

This gives Acyl-CoA by activation and is then transported across the inner mitochondrial membrane bound to the alcohol carnitine.

  • The Acyl CoA will react with carnitine to give acyl carnitine, this can then be transported through action of the enzyme ‘Translocase’
  • The acyl-carnitine is then broken down back into carnitine and releases the Acyl with the CoA that causes it to occur. This allows the molecule to get across the membrane.
18
Q

Fatty acid oxidation (b-oxidation)
(Liver mitochondria)

what is fatty acid oxidation, the generation of?

what it a series of? what does this breakdown series carry on till?

where does the acetyl-CoA enter? only in the presence of what? and only where?

how much atp does palmitate yield? what can you end up with if you cleave to an odd length?

odd number double bonds are removed by?
even number double bonds are removed by? (2)

what is the main production of fatty acid oxidation?
where can this be fed?

what actually happens to it?

A

Fatty acid oxidation is the reverse of synthesis, it is the generation of 2 carbon unit’s reformation of Acetyl CoA.

It is a series of oxidation, hydration, oxidation and thiolysis. The breakdown will continue until the chain length of the fatty acid reaches a certain length.

  • Beta-oxidation generates Acetyl-CoA, the Acetyl-CoA can enter the citric acid only in the presence of glycolysis to produce ATP. EXCEPT IN THE LIVER
  • Complete oxidation of palmitate yields 106 molecules of ATP.
  • There will be cleaving off the fatty acid until it reaches a certain chain length.
  • If you have an odd chain length, then you end up with proprionyl-CoA in last round of oxidation.
  • Odd numbered double bonds are removed by isomerase, even double bonds are removed by reductase and isomerase.

So, we can completely breakdown the fatty acids.
- So, in the liver the main production of fatty acid oxidation is for generation of Acetyl-CoA which can be fed into citric acid cycle to generate energy but doesn’t tend to be fed this way.

Rather, Acetyl-CoA tends to be converted to ketone bodies.

FADH2 and NADH form ATP

19
Q

Summary of fatty acid synthesis and degradation

where does synthesis take place? degradation?
where does it take place? 
what is added or removed?
oxidant/reducant?
carried out but what enzymes?
A
Synthesis
Cytosol
Intermediates linked to acyl-carrier protein
Sequential addition 2C
Reductant NADPH
Fatty acid synthase enzyme complex
Degradation
Mitochondria
Intermediates linked to coenzyme-A
Sequential removal 2C
Oxidants FAD and NAD
Carried out be individual enzymes
20
Q

Fatty acid degradation summary

when does it take place?

stiumulated by what hormones? (3)
inhibited by?

where does degradation take place?
where does beta oxidation take place?

what is it used to make in the liver?
what is it used to make in cardiac and skeletal muscle?

A

takes place in fasting state when glucose levels are low and/or when demand for ATP is high

Stimulated by glucagon, adrenalin and noradrenalin
Inhibited by insulin

Takes place in a number of tissues including the liver, kidney and muscle
Takes place in the mitochondria - β-oxidation

In the liver the main product acetyl-CoA is used for ketogenesis
In cardiac and skeletal muscle used to make ATP

21
Q

Ketogenesis (in the liver)

and the fate of ketone bodies

what is the acteyl coa converted to? whhat is that converted and what is that converted to?

what two things can happed to this? what are ketone bodies a mahor source of energy for?

what are the 2 fates of ketone bodies?

A
  1. Acetyl-CoA from breakdown of fatty acids is converted to Acetoacetyl-CoA
  2. Acetoacetyl-CoA is converted to HMG-CoA
  3. HMG-CoA is converted to acetoacetate

Acetoacetate can be reduced to 3-β-hydroxybutyrate or non-enzymatically to acetone.

Fate of Ketone Bodies

  1. The acetoacetate is converted in the non-hepatic tissue back to acetyl-CoA, this can then be used to generate ATP.
    o Ketone bodies are a major energy source for cardiac muscle and renal cortex.
  2. During starvation or diabetes 75% of the brains energy is derived from acetoacetate – the production of ketones increases with decreased food intake.
22
Q

Why does ketongenesis happen?

what 3 things stimulate fatty acid breakdown producing acetyl CoA?

what does metabolis shift towards during this?
what is decreased because of this? what is the effect of this? what will this formM

3 key ketone bodies?

A

Fasting, uncontrolled diabetes and prolonged exercise stimulates fatty acid breakdown producing acetyl-CoA

Metabolism shifts towards maintaining blood glucose leading to a reduction in OAA

Loss of OAA limits energy production from acetyl-CoA

Excess acetyl-CoA is used to form ketone bodies

Ketone bodies are acetoacetate, 3-β-hydroxybutyrate and acetone

23
Q

what regulates synthesis of ketone bodies?

when is ketogenesis high? why?

A

The synthesis of ketone bodies are regulated by the insulin/glucagon ratio.

Ketogenesis is high when the ratio is low as this inhibits acetyl-CoA carboxylase (rate limiting step in fatty acid synthesis).

24
Q

Fate of the Glycerol:

what does breakdown of triglycerides give? (2)

what absorbs the glycerol? what happens to it here?

what 4 steps happens to glycerol?

why is this a non-selfish use of glucsoe?

A

Breakdown of triglycerides gives acetyl-CoA and glycerol

The glycerol is absorbed by the liver and in the liver can be converted back to glucose.

  1. The glycerol gets phosphorylated to glycerol-3-phosphate
  2. Glycerol 3-phosphate oxidized to dihydroxyacetone phosphate
  3. Isomerised to glyceraldehyde 3 phosphate
  4. Glyceraldehyde 3-phosphate can go into glycolysis to produce ATP, but most of it goes into gluconeogenesis to synthesise glucose which will be released back into the circulation.

Fatty acid degradation occurs when the body is in need of an energy source, be that prolonged exercise, starvation etc.

Most of the glucose will be coming from here in these times, so it’s a non-selfish use of glucose as the liver doesn’t use it itself. Liver gets most of its energy from lipids/fatty acids.

25
Q

Summary of Lipid Breakdown

A
  1. TG are broken down to glycerol and fatty acids in adipocytes
  2. The glycerol is fed into glycolysis or gluconeogenesis (predominantly, glucose formed can then be transported to non-hepatic tissue)
  3. In the liver FA are activated and transported to the mitochondria
  4. FA are broken down in a step by step manner in to acetyl CoA
26
Q

Hormonal Regulation of Fat Metabolism

what 4 effects does insulin have?

what effect does glucagon and adrenaline have?

A

Insulin:
o Increases glycolysis in the liver (lower glucose levels by increasing removal of glucose from blood stream to most body cells
o Increases fatty acid synthesis in the liver
o Increases TG storage in adipose tissue
o Decreases beta-oxidation

Glucagon and adrenaline:
o Increases TG mobilisation (and so inhibits synthesis)