An enzyme-catalyzed reaction produces a product that has a maximum absorbance at 412 nm. The extinction coefficient is 4000 M-1 cm-1. A 10/1 dilution of the enzyme is made and 20 μL of the dilution are put into a cuvette with 80 μL of water and 1.9 mL of reaction cocktail. The absorbance change per minute is 0.05. Show your calculations for full credit.
a. How many units were in the cuvette if 1 unit = 1 μmol/min? (3)
b. How many units were in the cuvette if 1 unit = 1 nmol/min? (3)
c. What is the relative activity of the undiluted enzyme (1 unit = 1 μmol/min)?
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An enzyme-catalyzed reaction produces a product that has a maximum absorbance at 412 nm. The extinction...
Consider the enzyme-catalyzed reaction with Vmax=164 (μmol/L)min−1 and KM=32μmol/L. Part A If the total enzyme concentration was 6 nmol/L, how many molecules of substrate can a molecule of enzyme process in each minute? Express your answer to three significant figures. kcat kcat = 2.73×104 min−1 Part B Calculate kcat/KM for the enzyme reaction.
You have a 25 ml enzyme sample that has a total of 100 micro-moles/min of activity If you were to assay the enzyme, how much of it would you need in your assay in order to get an absorbance of 0.50 in a 30-minute assay. The product E=13,800M-1cm-1 and you are using a standard 1mL cuvette Beer-lambert law: A=CIE I=1
You have a 25 ml enzyme sample that has a total of 100 micro-moles/min of activity If you were to assay the enzyme, how much of it would you need in your assay in order to get an absorbance of 0.50 in a 30-minute assay. The product E=13,800M-1cm-1 and you are using a standard 1mL cuvette Beer-lambert law: A=CIE I=1
The following data were recorded for the enzyme-catalyzed reaction. Substrate concentration (M) 6.25 x 100 7.50 x 10 1.00 x 10-4 1.00 x 10-3 Reaction velocity (nM/min) 15 56 60 75 (1) Estimate Km and Vmax- (2) What would V be at S=2.5 x 10-5 ?
CHEM3250 Assignment-Enzyme Inhibition Consider the data below for an enzyme catalyzed reaction. The rate of the reaction has been determined with and without an inhibitor. A total concentration of enzyme of 20 uM was used in the experiment. SHOW WORK AND UNITS!!! Without Inhibitor With Inhibitor [substrate] (mM)Rate of formation of te of formation of product product (mM/min) mM/min) 6.67 5.25 0.49 7.04 38.91 1.0 2.2 6.9 41.8 44.0 1.5 3.5 1 a) On the same graph, plot the data...
Help on prelab
NOTE! There are FOUR (4) pages in this pre-lab! PRE-LAB WORKSHEET FOR ENZYME LAB To be completed prior to the online prelab esercise 1 ) Suppose that the diagram below represents what occurs during a chemical reaction e) Which letter points tq the prodact? print e ore , d 3) (c) Which letter points to the enzyme? (d) Which letter points to the enzyme's active site? (e) Which letter points to the enzyme's substrate? Note: Some letters...
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,...
1. Describe the functions of the following reagents in extraction of DNA from corn meal: proteinase K; guanidine HCI; SDS 2. Why is the ratio of the OD at 260 and 280 nm used to estimate DNA purity? 3. In one paragraph, summarize basic principles of PCR technique in your own words. List all the reagents you will need to perform a PCR experiment. Does this method tell you what genetic modifications were made? If yes, describe how you can...