Terminal Respiration Flashcards

1
Q

what is a hexos

A

A sugar/sacharride containing 6C’s

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2
Q

What can NAD+/FAD be classed as

A

Co-reactants - which are reduced by H- (hydride) ions containing high E electrons to form NADH/FADH2

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3
Q

What can then happen with NADH/FADH2?

A
  • Used in anabolism
  • Pass their High E e- through series of carrier P to yeild lots of ATP (term resp, oxi phosp, e- trans chain). High E e- eventually combine with O2 and form H2O
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4
Q

Where does oxidative phosphorylation occur in eukaryotes

A

Mitochondria

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5
Q

What’s the puropose of the mitochondria in relation to oxidative phosphorylation?

A

Allows coupling of oxidation of carbon fules to ATP sysnthesis
utilises proton gradients to produce ATP

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6
Q

Where must NADH/FADH2 be for terminal respiration

A

mitochondrial matrix

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7
Q

Where is the majoriyt of NADH/FADH2 formed

A

in mitochondrial matrix (e.g. CAC and B-oxiation of FA

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8
Q

Where else can NADH be formed

A

In the cytoplasm from glycolysis

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9
Q

How do we move cytoplasmic NADH into the mitochondrial matrix?

A

Shuttle used to move reducing equivalents accross the mitochondrial membrane (as cytoplasmic NADH can’t cross), but FADH2 can pass it’s e- onto the ETC withing the mitochondria. Process called glycerol phosphate suttle - reversiable oxidative process

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10
Q

Explain the glycerol phosphate shuttle

A
  1. NADH can’t cross mitochondrial membranes
  2. becomes oxidised to NAD+, reducing Dihydroxy acetone phospate to G3P
  3. G3P passes these e- across the membrane onto FAD, forming FADH2
  4. FADH2 can then be oxidised in the ETC

see sheet

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11
Q

How much energy is released by the osidation of FADH2 relative to NADH

A

Per mol, less ATP is generated by oxidation of FADH2 than NADH in the ETC. This means an energetic price is paid for using cytostosolic reduced co-substrates in terminal respiration

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12
Q

What does the ETC contain (name each)

A

4 complexes:
1. NADH-Q oxidoreductase
2. Succinate-Q reductase
3. Q-cytochrome c oxidoreductase
4. Cytochrome c oxidase

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13
Q

What does complex 1 NADH-Q oxidoreductase do?

A

Oxidises NADH and passes high-E e- to ubiquinone to give ubiquinol (QH2). Pumps H+ ions into the intermembranse space

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14
Q

What does complex 2 Succinate-Q reductase do?

A

Oxidises FADH2 and like 1 passes high-E e- to ubiquinone to give ubiquinol (QH2). Enzyme also part of CAC under guise of succinate dehydrogenase

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15
Q

What is Ubiquinone (Q)

A
  • Called Q10 in mitochondria (as has 10 isoprene repeats)
  • AKA coenzymeQ10
  • Dietary supplement - reduces free radicals so acts as antioxidant
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16
Q

What does complex 3 Q-cytochrome c oxidoreductase do?

A
  • Take e- from ubiquinol (QH2) annd passes them to cytochrome c (like heam)
  • 1 Qh2 is oxidised to yeild 2 reduced cytochrome c moleules
  • Pumps protons into intermembrane space
17
Q

What does complex 4 Cytochrome c oxidase do?

A
  • Take e- from cytochrome c and pass them to O2
  • e- channeled through Fe-Cu centre
  • Pumps protons into intermembrane space
18
Q

Where do NADH and FADH2 come from?

A
  • NADH: glycolysis, CAC, B-oxidation
  • FADH2: B-oxidation, (and HADH via G3P shuttle)
19
Q

how is energy conserved from the breakdown of food molecules

A

Ultimately leads to oxidation of NADH, FADH2, ubiquinone and cytochrome c. Energy further conserved through proton gradient across inner mitochondrial membrane

20
Q

How is enery stored up in proton grads used?

A
  1. Electron Motive Force - (actually proton motive force) - allows proton gradient to work
  2. A molecular turbin has evolved to harness the E in the proton gradient - ATP synthase
21
Q

Define Chemisosmosis and proton-motive force

A
  • As e- pass through complexes of the transport chain, protons move from matrix to outside of inner mitochondrial membrane - chemiosmosis
  • This movement has particular spatial directionality, so is classed as “vectoral”. Ex of energy transformation.
  • Protons on outside of membrane act as a store of Ep
  • When they are “allowed” to flow back down their grad they release E - Proton motive force
22
Q

Explain the process of ATp synthesis

A
  1. protons eventually flow down their conc grad back into the mitochondrial matrix
  2. Only a relatively small number of sites exist on membrane where this happen
  3. At these sites, multi-unit P called ATPsynthase (ATPase) is found
  4. ATPase has mechanism to allow protons to pass through
  5. As they flow, E stored in gradient used to Convert ADP+Pi to ATP
  6. ATP then stores this Ep and uses it to dow work in cells
23
Q

What is the structure of ATP synthase like?

A

Has 2 parts:
1. F0 - membrane bound proton conducting unit (10 subunits)
2. F1 - protudes into the mitochoindrial matric and acts as catalyst for ATP syntheses - produces lots of ATP from P-motive force energy collected by F0

24
Q

How does ATP synthase work?

A
  1. ADP+Pi enter B subunit
  2. Rotation of F0 cylinder and y shaft causes **conformational ** changes in B subunits of F1
  3. Catalyses ADP->ATP conversion and release ATP
25
Q

Explain the binding change mechanis of ATPase (briefly)

- not in course?

A

Sequential conformationsal changes of B subunit - 3 different binding pockets in 3 different states
By rotaion of F0 cylinder and y shaft all binding pockets run cyclic through the 3 states

26
Q

Why does NADH produce more ATP than FADH2 - stochiometry of oxidative phosphorylation

A

As e- pass through ETC, complexes 1,3,4 move total of 8H+ from matrix to outside of membrane. ATPase can produce 1ATP per 3H+ it moves back into the matrix across the membrane.

NADH feeds in at Complex 1 meaning e- pass through all 3 sites aloowing proton movement (Complex 1,3,4)
FADH2 feed in at Complex 2 so only 2 sites where protons move across the membrane are utilised,
Thus, 2.5mol and 1.5mol of ATP generated per mol of NADH and FADH2 respectively

27
Q

What are the products of respiration?

A

Food molecules completely broken down to CO2, H2O (and energy)
Some Ep from food molecules “saved” (after being transformed through reduced co-reactants and the terminal respiratory system) and is used to make ATP

28
Q

What is electron transport said to be coupled to?

A

ATP synthesis (coupled oxidative phosphorylation)

29
Q

What happens if e- transport is not couples to ATP synthesis?

A

If inner mitochondrial membrane becomes permeable to protons: proton grad not generated.
E- transport still occur (O2 reduced to H2O) but no ATP made.
Energy released from e- passing along the terminal respiratory system doesn’t make ATP bu is released as heat

30
Q

What diesase is caused from uncoupled e- transport and ATP synthase

A

Malignant hyperthermia - “leaky” mitochondrial membranes

31
Q

When could intentional uncoupling occur?

A

brown fat in newborn infants - cells have many mitochondria and if baby cold, nor-epinephrine triggers opening of channel protien called thermogenin which sits on inner mitochondrial membrane of brown fat cells - releases heat

32
Q

What does the proton gradient act as/do?

A

Store of energy and drives production of lots of ATP

33
Q

What 2 states can oxidative phosphorylation be?

A

Coupled or uncoupled

34
Q

What can coupling or uncoupling be a result off?

A

Intentionally or in disease states

35
Q

What is the final electron acceptor

A

Oxygen (forms 2 H20)

36
Q

2 parts of oxidative phosphorylation

A
  • Electron transport chain - first 4 proteins
  • Chemiosmosis - ATPsynthase part