Bioenergetics and Oxidative Phosphorylation Flashcards

1
Q

What is hydrolysis ? What does it provde ? What is the energy used for ?

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2
Q

ATP is considerd what ? Why is it favoriable to break them

?

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3
Q

What is Gibbs free energy formula, and what does each component mean ?

What is the mnemotic to remember ?

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good honey taste sweet

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4
Q

What does the charge of Delta G mean ? -,+, 0 ?

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5
Q

What is the formula of delta G, What does the * mean ? What is the full formula ?

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6
Q

What is the relationship between delta G and keq, what happens constant temp and pressure ? what is the value Delta when at equilibrium, what is the formula ?

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7
Q

What happens to Keq when greater 1 less 1 and 1 what does it mean ?

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8
Q

How does Delta G keep two consecutive reactions are additive ?

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9
Q

In mitochodnrial electron tranport chain, which of the two NADH or FADH2 gives the most energy ?

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10
Q

Where is the ETC located ? What is the purpose of oxygen ?

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11
Q

Where is the mitocondrial membranes located ? What is noteworthy of the inner mitochondrial membrane ?

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12
Q

Mitochondrial Matrix it has what kind of enzymes ? What does it synthesize ? What does the matrix contain ?

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13
Q

What are you producing from metabolism ? What does TCA make ? What is extraction of energy ?

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14
Q

What is NADH , where is it produced ? What role does it have in cytosolic NADH., what happens when oxidized ?

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15
Q

What is the purpose of FADH2, what is produced by ?

What type of shuttle does it use, and what is it similarl to ?

how can they be reoxidized by ?

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16
Q

What happens in the complex 1 ( NADH dehydrogenase , what does it have that allwos it to get electrons and hydrogen from NADH ? How many H and e, and what does it become ?

What is the fuction of Coenzyme Q (CoQ) role ?

Cytochromes contain ? How are electrons passed along the chain from CoQ to cytochromes bc1 (complex III)l,c,and a+a3(complex 4)

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17
Q

Draw the entire process of ETC

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18
Q

OXidative phosphorylation

What requires from to form ATP ? How is it regulated ?

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19
Q

OXidative phosphorylation

What requires from to form ATP ? How is it regulated ?

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20
Q

What are the components of complex 1 ? What is FMN ? How many electrons does it accept, How much does Fe-S electrons accept at a time ?

Wjhere are Fe-S centers located? and where does the electrons go ?

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21
Q

What is Complex 2 ( succinate dehydrogenase ) also part of ? Do they span the membrane ? Do they have a proton-pumping mechanism.

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22
Q

What is CoQ, is it protein bond ? What is it made out of ? How many electrons does it accept, what does it participate in ? Which complexes does it work ?

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23
Q

What is complex 3, where are the two electrons removed from ? at which site ? Where are the two molecules of cytochrome c ?

What does the Fe-S creates ?

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24
Q

ETC: Complex IV What is is called ? What does it have that name ? Where does it pass electrons ? What types of cytochrome does it contain, and why do they matter ? How many electrons per oxygen ?

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note that H20 has two hydrogens so 2 electrons, so to produce 2 H20 need 4 hydrogen=4 electrons

25
Q

The transfer of electrons down the ETC is favoriable how ? Does the transfer of electron from NADH to oxygen make ATP?

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26
Q

What is the role of proton pump? How is it coupled? What is created when hydrogen is in the intermembrane space ?

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27
Q

How many hydrogens are released per 4 e?

What abouut 1/2 oxygen ?

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28
Q

What does ATP synthase ? How are Protons move from F0 and what is f1

What is For rOtation ?

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29
Q

What is the F1, and Fo?

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30
Q

Where dooes ADP + P bind to ? Where does ATP bind ? what happens ?

What is it called?

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31
Q

What is uncouplers ?

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32
Q

What is the effect of uncoplers of protein gradient, ATP synthesis, Oxygen consumption, oxidation of NADH, and HEAT

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33
Q

What is UCP1(UnCoPelers)

What is it also called, where is it seen in humans ? what is it activated by ? What is the difference between brown fat vs white fat.

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34
Q

What are UCP2 used ? What is UCP3 used for ? What about UCP4 used for ? What does differnt levels of UCP3( SM) contribute to ?

What happens when there low levels of UCP ?

What happens in hyperthyroidism.

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35
Q

What synthetic uncouplers do ? What are the charge ?

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36
Q

What is 2,4 dinitrophenol ? How does it work

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synthetic uncouplers

37
Q

What happens to high doses of aspirin and other salicylates ?

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synthetic uncouplers

38
Q

how does cyanide act as a ETC inhibition ? How does one complex messing up, lead to the all of them ?

What inhibition of b-C1 complex do ?

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39
Q

Know it !

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40
Q

Know this!

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41
Q

Why is cyanide bad? What does it bind ? What is its connection to hydroxocobalamin ?

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42
Q

Where does carbon monocide bind to hinder ETC ? Where else ? What are symptoms ? Where are some sources of carbon monoxide ?

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43
Q

What are some reactive oxygen species ? How is an enzyme that breaks H2O2? When is the a higher amoutn of ROS ? How are Ross produced ? How can there be an increase of ROS ?

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44
Q

What are some causes of oxidative phosphrylation diseases ? How can it be caused by ?

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45
Q

What is Kearns-Sayre syndrome (KSS) When does it start, symtoms, and the mutation ?

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46
Q

Kearns Sayre Syndrome

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47
Q

What is MELAS, what is caused by , symtoms ?

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48
Q

What is leign disease ? When does it start? What are clinical manifestations ?

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49
Q

What is LHON diease ? What are the symtoms What type of mutation

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50
Q

READ and make a question

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51
Q
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