kinetics2 Flashcards

1
Q

Initial assumptions about michaelis-menton

A
  • k-2 is irrelevant bc theres no product
  • rate limiting step is k2 Vo = k2[ES]
  • [S] is constant
  • [ES] is constant steady state assumption
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2
Q

Vo =

A

Vmax[S]/(Km + [S])

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3
Q

1/Vo =

A

Km/Vmax[S] + 1/Vmax

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4
Q

Km =

A

(k2 + k-1)/k1

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5
Q

when k2

A

then Km = k-1/k1 which is the dissociation constant Kd so km would be a measure of the affinity of an enzyme for it’s substrate

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6
Q

Kcat

A

turnover number, number of product molecules per second (gives us an idea of how quickly the enzyme is actually going)

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7
Q

catalase

A

One of the fastest enzymes, very impressive turnover number, breaks down hydrogen peroxide(from oxygen), if you look at the reaction being catalyzed it gives you a clue as to why the kcat is so high

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8
Q

when [S]

A

Vo = kcat/Km * [Et][S]

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9
Q

kcat/Km is

A

a second order rate constant for the interaction of [Et] and [S]

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10
Q

The upper limit for Kcat/km

A

imposed by how fast E and S can diffuse together
(10^8M-1S-1)
an enzyme close to this limit is diffusion controlled and has reached catalytic perfection
(catalytic efficiency can’t be greater than this or it would break the diffusion control limit

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11
Q

arrhenius equation

A

Kcat = Aexp(-Ea/RT)

predicts that the enzyme rate doubles for every 10˚C increase in temperature until enzyme denatures

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12
Q

ternary comples

A

when an enzyme binds two substrates

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