lecture 5 Flashcards

1
Q

how are energetically unfavourable rxns driven?

A

rxn Y–>X is favoured,
we can still drive this rxn forward
(X–>Y) by siphoning off Y in another favourable rxn (Y–>Z)

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2
Q

energetically unfavourable rxns: what is the equilibrium?

A

Y is constantly being taken to make the product Z

you are left with a little X, a little Y and a lot of Z as the equilibrium

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3
Q

example: K= [Y]/[X]= 1/5
for the rx X–> Y

what happens to [Y] when you siphon off Y in the rxn Y–>Z

A

siphoning off Y cases the [Y] to be very low such that the ratio of Y/X is low

[Y]/[X]= 0.5/5

this causes the conversion of X–> Y to be favoured so that levels of X and Y can be brought back to levels at the equilibrium

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4
Q

molecules wander randomly into the cytosol in a process called

A

diffusion

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5
Q

what size of molecules diffuse slower?

A

larger molecules

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6
Q

what is important for diffusion in terms of the media

A

the viscosity of the media plays a role in diffusion speed

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7
Q

highly viscous media:

A

enzyme will never function at 100%
(less efficient)

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8
Q

How do we determine Vmax?

A

1/v= Km/Vmax??

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9
Q

Enzyme inhibition

A

competitive inhibitors compete for the activation site

competitive inhibitors have the same or v similar structure to the enzyme

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10
Q

enzyme inhibition: affinity

A

depending on the affinity of the substrate to the binding site

lower affinity= need more substrate to do the same thing

higher affinity= need less substrate to do the same thing

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11
Q

Enzyme inhibition is a major method that cells use to

A

regulate gene expression

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12
Q

enzyme inhibitors are important

A

pharmaceutical agents

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13
Q

competitive inhibitors: Km and Vmax?

A

Competitive inhibitors increase the Km but Vmax remains the same

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14
Q

why does Vmax remain the same with competitive inhibition?

A

Km will be different because you need a different amount of substrate to reach the same level

Vmax remains the same because you can add more substrate until it out competes the inhibitor

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15
Q

Examples of activated carriers

A

ATP
NADH
NADPH

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16
Q

Why are activated carriers reactive?

A

dipoles

phosphate-hydrogen bond is relatively unstable= able to give off energy easily

17
Q

How is energy captured using coupled reactions?

A

an energetically favourable rxn is used to drive an energetically favourable rxn

-cells have elaborate systems to capture energy from food

18
Q

NADH and NADPH general function

A

both are carriers of two high energy electrons and a proton (H+) that forms a hydride ion H-

19
Q

Why is it important that NADH and NADPH have different phosphate groups?

A

gives them a distinct shape and allows the binding of different sets of enzymes!!!!

but diff phosphate group does not affect the electron-transfer properties of NADH vs NADPH

20
Q

do NADH and NADPH have the same function?

A

NO! v similar molecule but diff functions

21
Q

NADH function

A

-catabolic rxns that generate ATP
-ratio of NAD+ to NADPH is HIGH

22
Q

NADPH function

A

-anabolic rxns
-ratio of NADP+ to NADPH is LOW

23
Q

Examples of NADH function

A

-NAD+ is reduced to NADH in the citric acid cycle
-Electrons from NADH are passed down the ETC to generate ATP

24
Q

Example of NADPH function

A

-biosynthesis of fatty acid
-biosynthesis of cholesterol

25
Q

How are activated carriers usually generated?

A

they are generated in rxns coupled to ATP hydrolysis

26
Q

Synthesis of biological polymers

A

synthesis usually needs energy input!

hydrolysis rxns are energetically favourable!