Enzyme Kinetics Flashcards

1
Q

What is enzyme kinetics?

A
The study of rates of chemical reactions catalyzed by enzymes
E+S-->ES-->E+P
- E=enzyme
- S=substrate
- P=product
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2
Q

What is the relationship between ES formed and E+S consumed in a steady state?

A

They are equal

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3
Q

Consuming all substrate results in free _____ and free _____

A

enzymes/products

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4
Q

What does V0 represent?

A

initial velocity (initial rate of reaction)

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5
Q

What does Vmax represent?

A

maximum velocity (reaction reaching plateau/saturation)

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6
Q

What does Km represent?

A

Michaelis-Menten constant, substrate concentration at 1/2 Vmax in mol

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7
Q

What is the Michaelis-Menten equation?

A

V0=(Vmax[S])/(Km+[S])

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8
Q

Km = ___ when V0 = ___

A

[S] / (1/2)Vmax

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9
Q

What type of graph can be used to determine the variables of the M-M equation?

A

a V0 vs. [S] graph

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10
Q

____ = rate of product production, = ___ in Km=([K2]+[K-1])/(K1)

A

Kcat / [K2]

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11
Q

K1=___–>___ rate, K2=___–>___ rate, K-1=___

A

E+S/ES/ES/E+P/E+S/ES

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12
Q

Enzyme eficiency constant = ?

A

= Kcat/Km

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13
Q

Kinetic _____ is the order of binding __ and releasing __, enzyme _____ allows distinguishing between kinetic ____ the more than one _____ is involved

A

mechanism/S/P/kinetics/mechanism/substrate

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14
Q

What are Lineweaver-Burk plots? What are the axis labels? What do the intercepts represent?

A

Linearized double-reciprocal plots for analyzing two substrate data or inhibition

  • plots 1/V0 vs 1/[S]
  • x-intercept=1/Km
  • y-intercept=1/Vmax
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15
Q

What are the types of kinetic mechanisms and how would you identify them on a L-B plot?

A

1) Sequential Kinetic Mechanism
a. Ordered: will show lines intersecting NOT on the y-axis
b. Random: will down lines intersecting at the y-axis
2) Ping Pong Kinetic Mechanism: shows parallel lines

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16
Q

What is enzyme inhibition and what are the types?

A

It is when enzyme activity is decreased by inhibitors

1) competitive
2) uncompetitive
3) mixed

17
Q

What is competitive inhibition and its characteristics?

A

Inhibitor binds to active site in competition with the substrate

  • Vmax: no change
  • Km: increase
  • L-B plot lines: intersect at y-axis
  • catalysis: unaffected
18
Q

What is uncompetitive inhibition and its characteristics?

A

Inhibitor binds to ES complex to inhibit substrate from binding

  • Vmax: decrease
  • Km: decrease
  • L-B plot lines: parallel
  • catalysis: inhibited
19
Q

What is mixed inhibition and its characteristics?

A

Inhibitor binds to regulatory site to inhibit substrate from binding

  • Vmax: decreases
  • Km: changed
  • L-B plot lines: intersect left of y-axis
  • catalysis: inhibited
20
Q

Which type of inhibitors permanently shut down the enzyme?

A

Irreversible inhibitors

21
Q

Which type of inhibitors can bind and dissociate from free enzymes or the ES complex?

A

Reversible inhibitors

22
Q

What are the types of enzyme regulators and their functions?

A

1) non-covalent/allosteric regulators: small chemicals that bind to the allosteric site and can improve or reduce enzyme function
2) covalent modification: either reversible or irreversible
a. reversible: uses signalling pathways to regulate PRO activity, can enter and exit
b. irreversible: activate zymogens/proenzymes (can be converted into enzymes when activated)