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29 Cards in this Set

  • Front
  • Back

Oxidation of fatty acids source of E

1/3 of our E comes from fats (triaglycerils)


About 80% of E used for the heart and liver are from oxidation of fatty acids


Hibernating animals rely on it

Fats provide efficient fuel

When compared with polysaccharides:


Carry mor E per C


Carry less water (nonpolar)


Glucose and glycogen are ST w quick delivery and fats are LT w slow delivery

Fatty acids are absorbed in the small intestines

See pic

Chylomicrons

Transport lipids in blood


Hormones trigger movement of stored triacylglycerols

Glucagon and epinephrine attach to receptor


Adenylyl Cyclades is then g coupled to covert ATP to cAMP


cAMP activated PKA


PKA targets 2 proteins: hormone sensitive lipase and HSL


This then activates ATGL which release a triacylglycerol, HSL breaks it doesn’t to diacylgylcerol and finally MGL redcues to monoacylglycerol so we have 3 fatty acids


Fatty acids are transferred out of cell

Lipase cleave fatty acids from glycerol

Need a way to use both the glycerol and the fatty acids chains


Glycerol will enter glycolysis

Glycerol from fats enters glycolysis

Glycerol kinase activate glycerol using ATP


Cost is covered in next steps


Allows limited anaerobic catabolism of fats

Glycerol is then oxidized

Glycerol 3-phosphate dehydrogenase is oxidized to create dihydroxyacetone phosphate

Transport or attachment to phospholipids conversion to fatty acyl-CoA

1. A phosphate from ATP is attached to prime/activate fatty acid


2. Now CoA-SH is able to bond with fatty acid and rest of phosphate group leaves


Creates a fatty acyl-CoA which can be used either to build up or break down fatty acids

Fatty acid transport into mitochondria

Degraded in cytosol of adipose cells and then transported to other tissues for fuel


Beta-oxidation of fatty acid occurs in mitochondria


Less than 12C can diffuse across membrane but larger need transport via acyl-carnitine/ carnitine transporter (molecule in pic)

Acyl-carnitine/carnitine transport

Enzyme on outside switches out for carnitine


Then goes through transport molecule (cotransporter: one goes in and one goes out).


Once in mitochondria, process is reversed

Fatty acid oxidation in mitochondria

Stage 1: oxidative conversion of 2 C units into acetyl-CoA via beta oxidation, creating NADH and FADH2


Stage 2: oxidation of acetyl-CoA into CO2 via citric acid cycle creating NADH and FADH2


Stage 3:generates 3 ATP from NADH and FADH2 via respiratory chain

Step 1: Beta oxidation pathway: dehydrogenation

Remove 2 C at a time


Occurs at beta C


Remove 2 e- into repository chain resulting in trans double bond

FAD cofactors in beta oxidation

Allows for transfer of H and e- to for FADH2

Step 2: hydration of alkene

Water adds across the double bond yielding alcohol on beta C

Step 3: dehtdrogenation of alcohol

Use another dehydranase to remove 2 e- and 2 H


Use cofactors NAD+ (where e- and H are going)

Contributions to respiratory chain

2e- from FAD cofactors


2e- from NADH cofactors

Step 4: transfer of fatty acid chain release

Now have less stable structure


acetyl-CoA released by thiol breaking C-C bond

For long chain fatty acids

Use trifunctional peptide that has all of the activities together for 12 C chains or more


I’m the short chain we have separated soluble enzymes

Oxidation of unsaturated fatty acids

Contain cis double bonds


Need additional enzymes:


Isomerase coverts cis double bonds starting at C 3 to trans double bonds (need for monounsaturated)


Reductase reduces cis double bonds not at C3 ( need both enzymes for polyunsaturated)


The mor double bonds you introduce, the less energy you get bc step is skipped resulting in less FADH

Odd numbered fatty acids

Some are odd number


Propionyl-CoA (3C ) forms during final cycle of beta oxidation of odd numbered fatty acids


Bacteria also produces it in rumen


Results in methylmalonyl CoA


Needs coenzyme B12 to succinylcholine CoA (swapping H)


Contains cobalt (like heme) called corrin

Beta oxidation in peroxisomes

Mostly in plants


Same steps but Difference in location of e-, Preference for long chain FA, And NADH can not be reoxidized

Pathway feedback

See pic

Omega oxidation

Happens at omega C in ER of liver and kidney


Mainly on substrates of 10 and 12 C


Minor pathway but becomes important when beta oxidation cannot occur due to carnitine deficiency

Alpha oxidation

is used to degrade branched FA chains


Occurs in peroxisomes

Ketone bodies

Need oxaloacetate is needed to get ACoA into citric acid cycle


When it is depleted m, ACoA is converted into ketone bodies


3 different ketone bodies exist

3 ketone bodies

In liver


Acetone:


Acetoacetate


Beta hydroxybutyrate

To make ketone bodies

1. (Reverse of last step in beta oxidation) Take 2 molecules of ACoA to make acetoacyl CoA


A third ACoA is added. This frees up 2 CoA molecules to move to other tissues


Break down to acetoacetate and further break down to acetone


All can be used for energy purposes and if in abundance, acetone can be released

Ketones bodies are made in kidney

See pic