BIOCHEMISTRY-ACHIEVE (1 TERM)
BIOCHEMISTRY-ACHIEVE (1 TERM)
9th Edition
ISBN: 9781319402853
Author: BERG
Publisher: MAC HIGHER
Question
Book Icon
Chapter 8, Problem 30P
Interpretation Introduction

(a)

Interpretation:

The values of Vmax and KM in the presence of inhibitorneeds to be determined.

Concept introduction:

The Michaelis-Menten equation relates the concentration of substrate with the velocity of the reaction. A constant which expresses the substrate’s concentration if the velocity of reaction equals to the half of the maximum velocity of the reaction is known as Michaelis-Menten constant. It is denoted by KM.

Expert Solution
Check Mark

Answer to Problem 30P

The values of Vmax and KM in the presence of inhibitor are 9.5μmol/min and 10.2μmol respectively.

Explanation of Solution

The given concentration of enzyme is 100μM.

The given data is showing the different values of velocity at different concentrations of enzymes in the presence and absence of inhibitor.

The value of Vmax without inhibitor is 47.6μmol/min.

The reciprocal values of substrate concentration [S] that is 1/[S], velocity with no inhibitor, 1/[V] and velocity with inhibitor, 1/[V]' (velocity with inhibitor)are calculated in the table given below.

[S] 1/[S] Velocity with no inhibitor 1/[V] Velocity with inhibitor 1/[V]'
3 1/3=0.33 10.4 0.097 2.1 0.48
5 1/5=0.2 14.5 0.069 2.9 0.34
10 1/10=0.1 22.5 0.044 4.5 0.22
30 1/30=0.033 33.8 0.029 6.8 0.15
90 1/90=0.011 40.5 0.024 8.1 0.12

The graph between 1/[S] and 1/[V]' is plotted as follows.

BIOCHEMISTRY-ACHIEVE (1 TERM), Chapter 8, Problem 30P

Figure 2

The slope of the above graph is shown by KM/Vmax which is calculated by using the expression as follows.

slope=y2y1x2x1

(1)

The values of y1,y2,x1 and x2 obtained from the graph are 0.48,0.34,0.33 and 0.2 respectively.

Substitute the respective values in equation (1).

slope=0.340.480.20.33=1.07

Thus, the value of slope is 1.07. Thus, the expression, of KM/Vmax equals to 1.07.

KM/Vmax=1.07

(2)

It is shown in the graph that yintercept is equal to 1/Vmax=0.105. Thus, the value of Vmax is calculated as follows.

Vmax=10.105=9.5μmol/min

Substitute the value of Vmax in equation (2).

KM/9.5μmol/min=1.07=1.07×9.5μmol/min=10.2μmol

Thus, the values of Vmax and KM in the presence of inhibitor are 9.5μmol/min and 10.2μmol respectively.

Interpretation Introduction

(b)

Interpretation:

The type of inhibition for the given enzymeneeds to be determined.

Concept introduction:

A molecule that disturbs or inhibits the activity of an enzyme is known as enzyme inhibitor. The enzyme inhibition stops the generation of enzyme-substrate complex which, in turn, inhibits the formation of the product. The three main types of inhibition are competitive inhibition, uncompetitive inhibition and noncompetitive inhibition.

Expert Solution
Check Mark

Answer to Problem 30P

The type of inhibition for the given enzyme is noncompetitive inhibition.

Explanation of Solution

In case of noncompetitive inhibition, there is no competition between inhibitor or substrate. Both substrate and inhibitor are able to bind to the active of enzyme simultaneously. In case of noncompetitive inhibition, the addition of inhibitor only decreases the value of Vmax without changing the value of KM.

According to the calculation for the predicting the values of Vmax and KM in the presence of inhibitor, the value of KM remains constant but there is a decrease in the value of Vmax. Thus, the type of inhibition for the given enzyme is noncompetitive inhibition.

Interpretation Introduction

(c)

Interpretation:

The dissociation constant for noncompetitive inhibitorneeds to be determined.

Concept introduction:

A molecule that disturbs or inhibits the activity of an enzyme is known as enzyme inhibitor. The enzyme inhibition stops the generation of enzyme-substrate complex which, in turn, inhibits the formation of the product. The three main types of inhibition are competitive inhibition, uncompetitive inhibition and noncompetitive inhibition.

Expert Solution
Check Mark

Answer to Problem 30P

The dissociation constant for noncompetitive inhibitor is 2.5×105M.

Explanation of Solution

The given concentration of enzyme is 100μM.

The value of Vmax without inhibitor is 47.6μmol/min.

The calculated value of Vmaxapp in the presence of inhibitor is 9.5μmol/min.

The value of dissociation constant for the noncompetitive inhibitor is calculated by the formula given below.

Vmaxapp=Vmax(1+[I]Ki)

(3)

Here,

  • Vmaxapp is the maximum velocity in the presence of inhibitor.
  • Vmaxis the maximum velocity in the absence of inhibitor.
  • Ki is the dissociation constant.
  • [I] is the concentration of enzyme.

Substitute the values of velocity in the presence and absence of inhibitor, value of kinetics in the above expression.

9.5μmol/min=47.6μmol/min( K i+100μM K i)9.5μmol/min=(47.6 μmol/minK i+( 47.6μmol/min)100μM K i)Ki=2.5×105M

Thus, the dissociation constant value is 2.5×105M.

Interpretation Introduction

(d)

Interpretation:

The fraction of the molecules of enzyme that contains a bound substrate in the absence and in the presence of 100μM inhibitorneeds to be determined.

Concept introduction:

A molecule that disturbs or inhibits the activity of an enzyme is known as enzyme inhibitor. The enzyme inhibition stops the generation of enzyme-substrate complex which, in turn, inhibits the formation of the product. The three main types of inhibition are competitive inhibition, uncompetitive inhibition and noncompetitive inhibition.

Expert Solution
Check Mark

Answer to Problem 30P

The fraction of the molecules of enzyme that contains a bound substrate in the absence and in the presence of 100μM inhibitor is 0.71.

Explanation of Solution

Given Information:

The given concentration of enzyme is 100μM.

The given concentration of substrate is 30μM.

The value of velocity, in the absence of inhibitor at [S]=30μM is 33.8μmol/min.

The value of velocity, in the presence of inhibitor at [S]=30μM is 6.8μmol/min.

The value of Vmax without inhibitor is 47.6μmol/min.

The calculated value of Vmaxapp in the presence of inhibitor is 9.5μmol/min.

Calculation:

The value of fraction of the molecules of enzyme that contains a bound substrate in the absence is calculated by the formula given below.

fES=VVmax

(4)

Here,

  • fES is the fraction of the filled active site.
  • V is the velocity in the absence of inhibitor.
  • Vmaxis the maximum velocity in the absence of inhibitor.

Substitute the values of velocity and maximum velocity in the absence of inhibitor in the equation (4).

fES=33.8μmol/min47.6μmol/min=0.71

Substitute the values of velocity and maximum velocity in the presence of inhibitor in the equation (4).

fES=6.8μmol/min9.52μmol/min=0.71

Thus, the fraction of the molecules of enzyme that contains a bound substrate in the absence and in the presence of 100μM inhibitor is 0.71.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
Biochemistry Question. Please help solve. Thank you! Based upon knowledge of oxidation of bioorganic compounds and howmuch energy is released during their oxidation, rank the following, from most to least, with respect to how much energy would be produced from each during their oxidation. Explain your placement for each one.
Biochemistry Question.For the metabolism of amino acids what is the first step for theirbreakdown? Why is it necessary for this breakdown product to be transported to the liver? For the catabolism of the carbon backbone of these amino acids, there are 7 entry points into the “standard” metabolic pathways. List these 7 entry points and which amino acids are metabolized to these entry points. Please help. Thank you!
Biochemistry Question. Please help. Thank you.   You are studying pyruvate utilization in mammals for ATP production under aerobic conditions and have synthesized pyruvate with Carbon #1 labelled with radioactive C14.   After only one complete cycle of the TCA cycle, which of the TCA cycle intermediates would be labeled with C14? Explain your answer.   Interestingly, you find C14 being excreted in the urine. How does it get there?
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Biochemistry
Biochemistry
ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher:W. H. Freeman
Text book image
Lehninger Principles of Biochemistry
Biochemistry
ISBN:9781464126116
Author:David L. Nelson, Michael M. Cox
Publisher:W. H. Freeman
Text book image
Fundamentals of Biochemistry: Life at the Molecul...
Biochemistry
ISBN:9781118918401
Author:Donald Voet, Judith G. Voet, Charlotte W. Pratt
Publisher:WILEY
Text book image
Biochemistry
Biochemistry
ISBN:9781305961135
Author:Mary K. Campbell, Shawn O. Farrell, Owen M. McDougal
Publisher:Cengage Learning
Text book image
Biochemistry
Biochemistry
ISBN:9781305577206
Author:Reginald H. Garrett, Charles M. Grisham
Publisher:Cengage Learning
Text book image
Fundamentals of General, Organic, and Biological ...
Biochemistry
ISBN:9780134015187
Author:John E. McMurry, David S. Ballantine, Carl A. Hoeger, Virginia E. Peterson
Publisher:PEARSON