BMS1030 - Glycogenolysis, Glycogenesis and Gluconeogenesis Flashcards

(23 cards)

1
Q

What is Glycogenolysis? What is it also known as? What enzyme is involved?

A

The process of getting glucose from storage.
Glycogen Catabolism.

Key enzyme = Glycogen Phosphorylase

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

What is the difference between a-Amylase and glucosidases?

A

a-Amylase - hydrolyses bonds at end of polypeptide chains (1,4 linkages)
Glucosidases - hydrolyses bonds at branch points (1,6 linkages)

forming smaller sugars

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

What is glycogen broken down into? By what enzyme?
What is it then converted into? How does this affect ATP yield?

A

Units of Glucose 1-phosphate

By glycogen phosphorylase

Converted into glucose 6-phosphate and enters glycolysis.
(Extra 1 ATP molecule preserved per G-6-P as one investment stage skipped)

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

What enzyme converts Glucose 1-phosphate into Glucose 6-phosphate?

A

Phosphoglucomutase - adds a phosphate to position 6 and removes phosphate from position 1.

This makes it usable as it can now enter glycolysis.

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

What is Glycogenesis? What is the key enzyme is involved?

A

Forming 1->4 glycosidic bonds in glycogen.

Glycogen synthase

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

How does glycogenesis occur? What is it stimulated by?

A

Glycogenin protein forms the core of a glycogen particle.
The first glucose is linked to a tyrosine -OH
Glycogen synthase attaches glucose units one at a time to form a structure (like a hairy ball of string).

Stimulated by G-6-P and insulin.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Why can’t we store and break down glycogen at the same time?

A

Because what stimulates one process inhibits the other.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is Gluconeogenesis? Why is it needed? Where does it occur?

A

The creation of new glucose.

Because very small/finite resources of glucose/glycogen in system.

Occurs in the liver.

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

What can gluconeogenesis form? What can it not form?

A

Can form: pyruvate, lactate, glycerol, AAs and all TCA intermediates

Cannot form: FAs - because FAs yield acetyl-CoA which cannot be converted back to pyruvate (irreversible step).

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

Why is gluconeogenesis not the reverse of glycolysis?

A

Because there are 3 irreversible steps that need to be bypassed.
Because the energetics of glycolysis mean you need to switch glycolysis off before turning on gluconeogenesis.

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

Ask Adam about formation of citrate and Pyruvate to Acetyl CoA slides.

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

Where does gluconeogenesis occur? What substrates cannot be used?

A

In the liver

Glucose created from many substrates but NOT fatty acids

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

In gluconeogeneis, which steps are the same (just in reverse) and which steps are replaced?

A

Steps 2 and 4-9 are the same.
Steps 1, 3 and 10 (the regulated steps) are replaced.

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

In gluconeogenesis, how is Pyruvate converted to PEP?

A

Via creating Oxaloacetate using Pyruvate carboxylase. And then converting Oxaloacetate to PEP using PEPCK enzyme.

Via a diversion into and out of the mitochondria.

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

In order for Oxaloacetate to cross the mitochondrial membrane, (from the matrix to cytosol) what occurs?

A

Oxaloacetate is converted to Malate (using an enzyme and NADH), carried across the membrane via a dicarboxylate carrier and then converted back into Oxaloacetate (using NAD+).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What does pyruvate carboxylase require?

A

ATP and bicarbonate as substrates
Biotin coenzyme
Acetyl CoA to activate it

High ATP and Acetyl CoA concentrations stimulate pyruvate to enter gluconeogenesis.

17
Q

Lots of ______ is needed to drive the reaction of PEPCK (convertng Oxaloacetate to PEP). In what 2 ways is it provided?

A

GTP (equivalent to ATP) is hydrolyzed.
Decarboxylation is a favourable reaction.

18
Q

In skeletal muscle, what does PEPCK allow for?

A

Storage of fatty acids as TGs - forming fat droplets which are used as energy reserves.

This creates a sustainable ATP supply to the working muscles.

Benefits = enhanced endurance, better weight management, appetite control and metabolic health.

19
Q

In Gluconeogenesis, how is Fructose-1,6-bisphosphate converted to Fructose 6-Phosphate?

A

Using the enzyme Fructose-1,6-bisphosphatase

(the reaction in opposite direction using PKF1 and is irreversible)

20
Q

What stimulates and inhibits Fructose-1,6-bisphosphatase enzyme? What kind of regulation is it?

A

GLUCAGON stimulates enzyme by decreasing fructose 2,6 bisphosphate.

ADRENALINE inhibits enzyme by increasing fructose 2,6 bisphosphate.

Allosteric regulation
- citrate
- fructose-2,6-bisphosphate
- AMP

22
Q

What organs do not carry out gluconeogenesis?

Where is Glucose-6-phosphotase found? How is G-6-P hydrolyzed? How is glucose released?

A

Brain and muscle does not carry out gluconeogenesis (as don’t have the enzymes).

In the ER of liver and kidney cells

G-6-P is hydroyzed as it passes into the ER.
ER vesicles filled with glucose diffuse to plasma membrane, fuse with it and open releasing glucose into bloodsteam.

23
Q

How is lactate converted back to glucose?

What is the cycle involved?

A

Lactate in muscle returned to liver and reoxidized to pyruvate by lactate dehydrogenase.

Pyruvate converted to glucose.

The Cori Cycle