Metabolism part 1 Flashcards

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1
Q

What is metabolism?

A

The complete set of catabolic (exergonic) and anabolic (endergonic) reactions that occur within living cells

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2
Q

Where is energy in ATP stored?

A

In the phosphoanhydride bonds

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3
Q

How do we obtain energy?

A

Through the oxidation of organic molecules (food)

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4
Q

What is the difference between NAD and NADP?

A

NADP has a phosphate
The molecules pick up energy in the form of 2 high energy electrons and a proton - hydride ion

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5
Q

What is glycolysis and when does it occur?

A

Obtaining energy from glucose
Consists of 10 steps
Occurs in both aerobic and anaerobic conditions

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6
Q

What is step 1 of glycolysis?

A

Glucose is trapped in the cell and it is phosphorylated by hexokinase which adds a phosphate from ATP hydrolysis. This forms glucose 6 phosphate which cant leave the cell

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7
Q

What is step 2 of glycolysis?

A

Glucose 6 phosphate undergoes isomerisation to form fructose 6 phosphate

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8
Q

What is step 3 of glycolysis?

A

The fructose 6 phosphate is phosphorylated to form Fructose 1,6 bisphosphate catalysed by PFK

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9
Q

What is step 4 and 5 of glycolysis?

A

Aldolase splits the F 1,6 BP into G-3-P and DHAP but DHAP is not on the glycolysis pathway but is an isomer of G-3-P so is converted to it

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10
Q

What is the importance of converting from glucose to fructose?

A

It would have split into 2 x isomers (2 and 4C molecules instead)

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11
Q

What is step 6 of glycolysis?

A

Enzyme 1 binds to the G-3-P and catalyses its oxidation
NAD+ accepts the electrons and is reduced
The enzyme is displaced by Pi to create a high energy sugar phosphate (1,3- bisphosphoglycerate)

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12
Q

What is step 7 of glycolysis?

A

The intermediate binds to enzyme 2 which catalyses the transfer of Pi to ADP
thus creating ATP and generating a carboxylic acid 3-phosphoglycerate

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13
Q

What is step 8 of glycolysis?

A

3- phosphoglycerate is converted to its isomer 2 - phosphoglycerate

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14
Q

What is step 9 and 10 of glycolysis?

A

2- phosphoglycerate loses a molecule of water becoming phosphoenolpyruvate (PEP) which is unstable so donates a phosphate group to ADP forming ATP and PEP is converted to pyruvate.

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15
Q

Where does lactate come from?

A

In anaerobic cells glycolysis is the principle source of ATP
NAD must be regenerated to enable glycolysis to continue
When no O2 can act as the final electron acceptor NADH passes electrons to pyruvate to form lactate

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16
Q

How is PFK regulated?

A

Regulatory molecules bind to the allosteric site to either increase or decrease the affinity of PFK for F-6-P
Activated by - AMP, F 2,6 BP
Inhibited by - ATP, decrease in pH and citrate

17
Q

What is gluconeogenesis?

A

Occurs in the liver and is the formation of glucose from non carbohydrate precursors e.g. lactate, glucogenic amino acids

18
Q

Why is gluconeogenesis not the reverse of glycolysis?

A

It would be energetically unfavourable

19
Q

What is step 1 of gluconeogenesis?

A

The mitochondria converts pyruvate to oxaloacetate by pyruvate carboxylase which adds CO2 as it has a biotin prosthetic group

20
Q

What is step 2 of gluconeogenesis?

A

Oxaloacetate is converted to malate which can leave the mitochondria (very impermeable) it is then converted back to oxaloacetate in the cytosol by NADH. This is then converted into PEP

21
Q

What is step 3 of gluconeogenesis?

A

The reverse of glycolysis occurs and fructose 1-6 bisphosphate forms it is then converted to fructose 6 phosphate which is isomerised to form glucose 6 phosphate which is then converted to glucose

22
Q

How is glycolysis and gluconeogenesis regulated?

A

Glycolysis generates ATP so AMP activates glycolysis and inhibits gluconeogenesis

23
Q

What is the Cori cycle?

A

During heavy exercise - high glycolytic flux in the muscles- lactate can enter the blood and then enter the liver where it undergoes gluconeogenesis converting it back to glucose

24
Q

Outline the entry into the TCA cycle

A

Pyruvate moves into the mitochondria where pyruvate dehydrogenase complex converts it to acetyl co A
It does this by decarboxylating it, then it is oxidised by NADH, co enzyme A is added forming acetyl co A

25
Q

Outline the TCA (Krebs) cycle

A

Citrate synthase sequentially binds a 4C oxaloacetate then the 2C acetyl co A which forms an enol bond and forms citryl CoA which citrate synthase can break down to form a 6C citric acid and prevents acetate and co A forming
Energy is released and captured by - 3x NADH, 1x FADH2, 1x GTP

26
Q

How is the TCA cycle regulated?

A

Matched to the cell’s energy need
2 enzymes can be allosterically regulated
Isocitrate dehydrogenase
stimulated by ADP NAD
Inhibited by ATP NADH
Alpha ketoglutarate dehydrogenase
Stimulated by ADP
Inhibited by ATP NADH

27
Q

How does the TCA cycle aid biosynthesis?

A

Citrate can been taken out to form fatty acids
Oxaloacetate can be taken out to form amino acids

28
Q

What is anapleurosis?

A

Reactions that replenish the TCA cycle intermediates

29
Q

What is an example of anapleurosis?

A

Oxaloacetate drawn off the TCA cycle for amino acid synthesis, increase acetyl coA which increases pyruvate carboxylase activity which increases oxaloacetate thus increasing TCA flux.