velocity (rate of formation Velocity with 10 mg/ml ibuprofen (mM/min) [arachidonic acid] (mM) 1/[S] 1/v 1/v (mM) (mM/min with ibuprofen (mM/min of PGG,) (mM/min) 23.5 0.5 1.0 1.5 2.5 3.5 16.67 25.25 30.49 37.04 38.91 2.00 0.0426 0.0311 0.0271 0.0239 0.0227 0,0600 0.0396 1.00 0.667 0.400 0.286 32.2 36.9 41.8 44.0 0.0328 0.0270 0.0257 Use a Lineweaver-Burk plot (double reciprocal plot) on the graph paper below to determine K, and V in the absence and in the presence of ibuprofen. Show your work/reasoning, and state units for all numerical answers.

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Chapter1: Biochemistry: An Evolving Science
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How does one plot the lineweaver burk plot using this data.

(This is taken mainly from Lehninger Principles of Biochemistry, 6th ed., ch. 6, #12, p. 239.)
The kinetic data below are for the cyclooxygenase reaction catalyzed by prostaglandin H2 synthase
("COX"), producing prostaglandin G2, the precursor of other prostaglandins and of thromboxanes.
Velocity was measured as a function of the concentration of the substrate arachidonic acid in the
absence and in the presence of 10 mg/ml ibuprofen (Cı13H1802). The molecular mass of the
undissociated acid form of ibuprofen is 206 g/mol. (Structure of the anionic form is on p. 846 of
Lehninger Principles of Biochemistry, 6th ed.) The reciprocals of velocity and of [substrate] have
been calculated for you!
[arachidonic acid]
(mM)
1/[S]
velocity (rate
of formation
1/v
Velocity with
10 mg/ml
ibuprofen
(mM/min)
1/v
(mM):
(mM/min
with ibuprofen
of PGG.)
(mM/min
(mM/min)
23.5
32.2
36.9
0.5
2.00
0.0426
16.67
0.0600
1.0
1.00
0.0311
25.25
0.0396
1.5
0.667
0.0271
0.0239
0.0227
30.49
0.0328
0.0270
0.0257
2.5
0.400
41.8
37.04
3.5
0.286
44.0
38.91
Use a Lineweaver-Burk plot (double reciprocal plot) on the graph paper below to determine K, and
V in the absence and in the presence of ibuprofen. Show your work/reasoning, and state units
for all numerical answers.
Transcribed Image Text:(This is taken mainly from Lehninger Principles of Biochemistry, 6th ed., ch. 6, #12, p. 239.) The kinetic data below are for the cyclooxygenase reaction catalyzed by prostaglandin H2 synthase ("COX"), producing prostaglandin G2, the precursor of other prostaglandins and of thromboxanes. Velocity was measured as a function of the concentration of the substrate arachidonic acid in the absence and in the presence of 10 mg/ml ibuprofen (Cı13H1802). The molecular mass of the undissociated acid form of ibuprofen is 206 g/mol. (Structure of the anionic form is on p. 846 of Lehninger Principles of Biochemistry, 6th ed.) The reciprocals of velocity and of [substrate] have been calculated for you! [arachidonic acid] (mM) 1/[S] velocity (rate of formation 1/v Velocity with 10 mg/ml ibuprofen (mM/min) 1/v (mM): (mM/min with ibuprofen of PGG.) (mM/min (mM/min) 23.5 32.2 36.9 0.5 2.00 0.0426 16.67 0.0600 1.0 1.00 0.0311 25.25 0.0396 1.5 0.667 0.0271 0.0239 0.0227 30.49 0.0328 0.0270 0.0257 2.5 0.400 41.8 37.04 3.5 0.286 44.0 38.91 Use a Lineweaver-Burk plot (double reciprocal plot) on the graph paper below to determine K, and V in the absence and in the presence of ibuprofen. Show your work/reasoning, and state units for all numerical answers.
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