The Citric Acid Cycle and Terminal Respiration Flashcards

(34 cards)

1
Q

where does citric acid cycle occur

A

mitochondrial matrix

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2
Q

where do electrons go after the CAC

A

passes them on to form NADH and FADH2

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3
Q

what is oxidization

A

the loss of electrons

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4
Q

where does Acetyl CoA come from

A

pyruvate from glycolysis and fatty acids are oxidized further to produce Acetyl CoA

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5
Q

how many molecules of ATP comes from one molecule of glucose

A

2

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6
Q

why is it dangerous for too much oxygen molecules

A

free radicals forming

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7
Q

electrons from the citric acid cycle (and before) binds with electron carriers to ultimately produce what

A

water

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8
Q

what do the electrons from the citric acid cycle (and before) combine with to produce water

A

protons and molecular oxygen

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9
Q

in simple terms, what does the acid citric cycle do

A

to harvest electrons to oxidise food molecules to CO2 and H2O

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10
Q

how is pyruvate dehydrogenase regulated

A

by its intermediate products and ATP (from the end point of cellular respiration)

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11
Q

if the cell has enough energy, what molecules regulate the pyruvate dehydrogenase complex

A

ATP, Acetyl CoA and NADH

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12
Q

if the cell needs more energy, what molecules regulate the pyruvate dehydrogenase complex

A

pyruvate and ADP

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13
Q

blocking isocitrate dehydrogenase causs what

A

citrate build up

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14
Q

what are the consequences of citrate build up

A

citrate will shuttle into the cytoplasm causing PFK1 to stop glycolysis

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15
Q

what can activate pyruvate carboxylase

A

the build up of acetyl CoA

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16
Q

what does anaplerotic mean

A

Greek work meaning to fill up

17
Q

where is the only site of oxidative phosphorylation in eukaryotes

A

mitochondria specifically in the mitochondrial matrix

18
Q

where does beta-oxidation happen in the cell

A

mitochondrial matrix

19
Q

what does oxidoreductase do

A

oxidises one thing while reducing some thing else

20
Q

what is in the middle of a oxidoreductase complex

A

iron-sulfur centres

21
Q

what is the purpose of iron-sulfur centres

A

to allow electrons to pass through the (oxidoreductase) complex and eventually passing the electrons to ubiquinone (Q)

22
Q

what does the heme group do in complex 2 in the electron transport chain

A

it blocks stray e-‘s that are coming up from the iron-sulfur centres

23
Q

if the heme group in complex 2 is deformed, what can happen?

A

electrons can start forming free radicals of O2 (superoxide) - leading to paraganglioma (in some tissues)

24
Q

what is paraganglioma

A

benign tumours in the head and neck - particularly in the carotid body

25
how many reduced cytochrome c is made from oxidising one ubiquinol
2
26
in complex 4 in the electron transport chain, how do electrons pass through
they go through iron-copper centres
27
hoe do the energy stored up in the H+ gradient used
proton motive work (the chemical charges on either side of the membrane and pH differences) AND molecular turbine
28
what is chemiosmosis
the movement of protons from the one side of a membrane to the other
29
ATPase described in detail
two parts: F0 and F1, F0 rotates, F1 had 6 sub units (3 alpha and 3 beta), gamma subunit on the middle (where electrons pass through to bind with ADP and Pi
30
what subunit does the ADP and Pi enter in the ATPase
beta subunit
31
why does F0 rotate in ATPase
to separate the ATP from the beta subunit
32
what is malignant hyperthermia
diseased caused by leaky mitochondrial membranes that uncouple electron transport and ATPase
33
what does halothane do
it causes leaky inner mitochondrial membranes in muscle leaky in some way
34
intentional uncoupling of ATPase and ..., what happens
nor-epinephrine triggers the opening of a channel in a protein called thermogenin. Breaks the gradient and protons come in and out of the matrix. the energy that would have been stored is released as heat