Enzymes and Enzymes Kinetics Flashcards

1
Q

Enzyme Classification

A

Oxidoreductases: Oxidation-reductions

Transferases: Functional group transfer reactions

Hydrolases: Hydrolysis reactions

Lyases: Reactions involving group elimination to form double bonds

Isomerase: Isomerisation reactions

Ligases: Reactions involving bond formation coupled with ATP hydrolysis

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2
Q

Forces that determine substrate specificity

A

Van der Walls forces such as:
hydrogen bonding
charge-charge (electronic) interactions
hydrophobic interactions

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3
Q

Binding of substrate is due to —————————————————

A

van der Walls, electrostatic, hydrophobic interactions

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4
Q

Cu2+, Fe2+, Zn2+
are…..

A

Cofactors

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5
Q

(organic molecules) NAD, FAD, Co-Enzyme A are:

A

Coenzymes or Co-Substrates

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6
Q

Heme group in cytochrome c

A

Prosthetic groups

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7
Q

———— the rate of a reaction (varies with reactant concentration)

A

Velocity (v)

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8
Q

———— indicates the speed or efficiency of a reaction

A

Rate constant (k)

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9
Q

Rate equation: v = k[S1]1[S2]1
For reactions: S1 + S2 P1 + P2

A

Second order reaction
Rate is determined by the concentration of both substrates

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10
Q

D[P] / Dt = v = k[S]

A

First Order Rate Equation

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11
Q

S1 + S2=P1 + P2
v = k[S1]1[S2]0 = k’[S1]1

If the concentration of one reactant is so high that it remains essentially constant, reaction becomes zero order with respect to that reactant

Overall reaction is ————————–

A

pseudo first-order

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12
Q

complex formed when specific substrates fit into the enzyme active site

A

Enzyme-substrate complex (ES)

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13
Q

When [S]&raquo_space; [E], every enzyme binds a molecule of substrate (enzyme is saturated with substrate)
Under these conditions the rate depends only upon [?], and the reaction is ————–

A

Enzyme
pseudo-first order

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14
Q

Enzyme-catalyzed Reaction can be monitored by:

A

Formation of a product or disappearance of substrate.

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15
Q

Velocity at the beginning of an enzyme-catalyzed reaction is

A

Initial velocity (vo)

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16
Q

Michaelis Menten Equation

A

Vmax[S]
v =
Km + [S]

Equation describes v versus [S] plots
Km is the Michaelis constant

17
Q

————–: expressed µmoles of product formed per minute per milligram protein and is designated as IU (International Units)

A

Enzyme activity

18
Q

————- is reached when an enzyme is saturated with substrate (high [S])

A

Maximum velocity (Vmax)

19
Q

At high [?] the reaction rate is independent of [s] (zero order with respect to s)

A

Substrate

20
Q

At low [?] reaction is first order with respect to S

A

Substrate

21
Q

The shape of a v versus [S] curve is a rectangular hyperbola, indicating:

A

saturation of the enzyme active site as [S] increases

22
Q

Substrate concentration at which reaction velocity is half-maximal

A

Michaelis constant (Km)

23
Q

Smaller the Km, an enzyme achieves Vmax at ——-substrate concentration

A

lower
hence the enzyme is more efficient

24
Q

T or F
Km is dependent on temperature and pH

A

T

25
Q

Substrates (substances) that reduce an enzyme’s activity are know as

A

inhibitors
- Reversible inhibition
- Irreversible inhibition - inactivates the enzyme

26
Q

Types of enzyme inhibitors

A

Competitive inhibitors
Un-competitive inhibitors
Non-competitive inhibitors

27
Q

Inhibitor binds only to free enzyme (E) not (ES)

A

Competitive Inhibition

28
Q

T or F
Vmax is the same with or without I (high S can still saturate the enzyme even in the presence of I)

A

T

29
Q

T or F
Apparent Km measured in the presence of I is larger than Km (in absence of I)

A

T

30
Q

T or F
Competitive inhibitors does not resemble the substrate

A

F