Energy: Carbohydrates 3 Flashcards

1
Q

TCA cycle

central pathway in catabolism

A

Mitochondrial (aerobic)

  • oxidative (requires NAD+, FAD+)
  • some energy is produced via SUBSTRATE LEVEL PHOSPHORYLATION
  • produces some precursors for biosynthesis
  • 2 cycles for every one glucose entering glycolysis (6NADH, 2FADH2, 2GTP, 4CO2)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Regulation of TCA cycle

A

Regulated by energy availability (ATP/ADP ratio) and (NADPH/NAD+ ratio)

  • activated by ADP
  • inhibited by NADH, ATP
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Pyruvate dehydrogenase (PDH)

A

Pyruvate (3C) is converted to acetyl CoA (2C) which can then enter the TCA cycle
- happens in the mitochondrial matrix (pyruvate is hydrophilic so has to be transported from the cytoplasm across the mitochondrial membrane)
- PDH is a large multi enzyme complex
- is sensitive to vitamin B1 deficiency as the enzymes require various cofactors
- the reaction is irreversible (loss of CO2) so is a key regulatory step (pyruvate cannot be formed from acetyl CoA
Deficiency leads to lactic acidosis

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

TCA supplying Biosynthetic processes

can convert substrates from one form to another to aid in metabolism

A
Amino acids can enter and leave the TCA cycle in four different places
Fatty acids (from citrate), haem (from succinate) and glucose (from oxaloacetate)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Catabolism of glucose up to the end of the TCA

A
  • all C-C and C-H bonds have been broken
  • all C atoms have been oxidised to CO2
  • all H atoms have been transferred to NAD+ + FAD
  • some substrate level phosphorylation (net 2 ATP)
  • NADH + FADH2 have large amounts of reducing energy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

ETC

A
  • mitochondrial (electron transport and ATP synthesis)
  • NADH and FADH2 are reoxidised
  • oxygen is the final electron acceptor (reduced to H2O)
  • large amounts of energy produced by oxidative phosphorylation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Uses of reducing power in ATP synthesis

A
  • electrons on NADH and FADH2 are transferred through a series of carrier molecules to oxygen - ELECTRON TRANSPORT
  • free energy is used to drive ATP synthesis - OXIDATIVE PHOSPHORYLATION
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Mitochondrial electron transport

A
  • NADH+H+ gives its (2H+e-) to the proton translocating complex (PTC) 1
  • FADH2 gives its (2H+e-) to PTC2
    The (2) hydrogen ions are pumped across the inner membrane into the inner membrane space using the energy (30%) from the (1) electrons by proton pumps creating a high proton motive force (pmf) in the inner membrane space (a proton gradient)
  • the final electron acceptor is oxygen - which makes water
  • H+ then flows back down its concentration gradient into the matrix via ATP synthase (as the membrane is impermeable to H+) - this generates ATP
    The energy from the dissipation of the pmf is coupled to the synthesis of ATP
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Reducing energy potential

A
  • electrons in NADH (uses 3 PTCs) have more energy than in FADH2 (uses 2 PTCs)
    The oxidation of 2 moles of NADH = 5 moles of ATP
    the oxidation of 2 moles of FADH2 = 3 moles of ATP
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Regulation of oxidative phosphorylation

A

When ATP concentration is high, (ADP concentration is low), there is no substrate for ATP synthase

  • inward flow of H+ stops
  • concentration of H+ in the mitochondrial space increases
  • prevents further H+ pumping as energy available in the electrons is insufficient
  • stops the ETC
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Inhibition of oxidative phosphorylation

A
  • inhibitors block electron transport e.g. Cyanide (CN-) prevents the acceptance of electrons by O2
  • ETC backs up and stops
  • poisoning of the terminal PTC, electrons have no where to go, H+ are not pumped out, the pmf decreases, not enough energy to make ATP
  • results in death as there is insufficient ATP to sustain life
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Uncoupling of oxidative phosphorylation

A

UNCOUPLERS increase the permeability of the mitochondrial inner membrane to protons - they no longer have go through ATP synthase

  • reduced pmf
  • no drive for ATP synthase
  • energy lost as heat
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Brown adipose tissue

A
  • in the back of the neck
    The degree of coupling is controlled by fatty acids - allows for extra heat generation
  • contains thermogenin (UCP1)
    In response to cold noradrenaline activates:
    LIPASE –>releases FA from TACs
    FA activate UCP1 (which transports H+ back into the mitochondria
  • energy of pmf is released as heat
    Important in NEWBORN INFANTS and HIBERNATING ANIMALS for non-shivering thermogenesis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Phosphorylation

A
SUBSTRATE LEVEL 
- cytoplasmic and mitochondrial matrix
- energy directly through hydrolysis 
- can occur limitedly in the absence of oxygen 
- minor process for ATP synthesis 
OXIDATIVE 
- inner mitochondrial membrane 
- energy indirectly through pmf
- cannot occur in the absence of oxygen
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

ATP synthesis from glucose

A
GLYCOLYSIS
- 2 ATP
- 2 NADH = 5 ATP
Pyruvate dehydrogenase 
- 2 NADH = 5 ATP
Kreb's cycle 
- 2 GTP = 2 ATP 
- 6 NADH = 15 ATP 
- 2 FADH2 = 3 ATP 

TOTAL = 32 ATP per 1 moles of glucose

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