1. Maximum velocity is reached when all the substrate is occupied by enzyme. So, it will be 0.1 M/s.
Vmax = 0.1 M/s
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1. an enzyme is observed to approach an initial velocity of 0.1M/s as more and more...
ISU Question 3: Use the data below to construct a Michaelis-Menton curve of velocity vs. [S]. This is quite easy to do in Excel. Vo 1/[S1 1/V0 UM (UM/s) M (s/uM) 340 10 2.94E-03 0.2 530 740 0.8 910 1.6 1040 0.4 a) Estimate Vmax from your curve. b) Describe any difficulty you have in completing part (a). Is the enzyme saturated at the highest (SD? c) Using your Vmax estimate, calculate 14 Vmax, and using your curve, estimate Km....
Can help me with these questions please. 30. Sphingosine-1-phosphate (S1P) is important for cell survival. The synthesis of S1P from sphingosine and ATP is catalyzed by the enzyme sphingosine kinase. The velocity of the sphingosine kinase reaction was measured in the presence and absence of threo-sphingosine, a stereoisomer of sphingosine that inhibits the enzyme. The results are shown below. Sphingosine (uM) vo (mg /min) vo (mg /min) with inhibitor 2.5 32.3 8.5 3.5 40 11.5 5.0 50.8 14.6 10 72...
1-The unmutated form of your protein has a Km of 25 µM and a Vmax of 43 mM/s. The enzyme kinetic data for your enzyme with the amino acid substitution should now be displayed in the table above. Based on these data, explain the effect of amino acid substitution on the Km and Vmax for the mutated protein. (Up to 50 words) You are not expected to draw a Lineweaver-Burk plot, however a quick sketch of a Vi vs [S]...
cat 2 14. You measure the kinetics of an enzyme E as a function of substrat using the double-reciprocal (Lineweaver-Burk) plot (Figure maintained constant at a level of 1 M (-106 M) e concentration and plot the data below). The enzyme concentration is S]. Vo. 2.9 4.4 5.4 5.8 6.2 6.4 0.15 00s 10 1/Is]. 10* M From these data, determine Vmax, KM, kcat and the turnover number for the enzyme. Determine these parameters by two different methods: (1) from...
how do you make a lineweaver-burk plot where the trend line extends backwards? is there a way of figuring out how far back it should extend based of your data ? As well, how do you plot two sets of data on one graph ? Thank you! (idk if you need to see my data-> attached below) Biochemistry Enzyme Kinetics Assignment Four answers for this assignment will be completed in elearn: En in elearn: Enzyme Kinetics Quiz ots but must...
Valganciclovir was synthesised from ganciclovir (1) using an esterase enzyme in an organic solvent giving two isomers as shown in the scheme below: esterase enzyme in organic solvent NA NH HN HO ganciclovir N unwanted isomer During this reaction, inhibition of the esterase enzyme was observed and it was proposed that the cause of this was binding of the unwanted isomer (2). In order to test this hypothesis, 2 was added to the reaction mixture. The data obtained from these...
Suppose that the following data are obtained for an enzyme-catalyzed reaction: [S] (mM) V (mmol ml-1min-1) 0.1 3.33 0.2 5.00 0.5 7.14 0.8 8.0 1.0 8.33 2.0 9.09 a.) From a double-reciprocal plot of the data, determine Km and Vmax. b.) Assuming that the enzyme present in the system had a concentration of 10-6 M, calculate its turnover number.
Please help me with these two problems. I will rate the answers. 1. The HIV-1 protease, an important enzyme in the life cycle of the human immunodeficiency virus-1 (HIV-1), is a good drug target for the treatment of HIV and AIDS. A protein produced by the virus, p6*, is an HIV-1 protease inhibitor. The activity of the HIV-1 protease was measured in the presence and absence of p6* using an assay involving an artificial substrate, as shown below. NH Lys...
Based on the document below, 1. Describe the hypothesis Chaudhuri et al ids attempting to evaluate; in other words, what is the goal of this paper? Why is he writing it? 2. Does the data presented in the paper support the hypothesis stated in the introduction? Explain. 3.According to Chaudhuri, what is the potential role of thew alkaline phosphatase in the cleanup of industrial waste. CHAUDHURI et al: KINETIC BEHAVIOUR OF CALF INTESTINAL ALP WITH PNPP 8.5, 9, 9.5, 10,...
only need answer for question d and e. thanks 2. Captopril was the first of a class of blood pressure lowering drugs that work by reversibly inhibiting Angiotension-converting enzyme (ACE). Later to the market was Lisinopril. This class of drugs is the fifth most prescribed, approaching 200 million prescriptions per year in the US alone. ACE inhibitors work by preventing the proteolytic cleavage of angiotensin I by ACE to create its active form angiotensin II, which binds to receptors in...