Question

If you double the amount of enzyme present in your activity assay, should the activity double?...

If you double the amount of enzyme present in your activity assay, should the activity double? Why or why not?

Homework Answers

Answer #1

An enzyme (Catalase) is a biological catalyst. It can modify the rate of reaction without being changed itself. Every enzyme are capable of converting one kind of substrate molecule into one kind of product molecule, which forms the enzyme-substrate complex. If we increase the amount of enzyme present in our activity assay, it enhances the rate of reaction because there are a greater number of active sites accessible for the enzyme-substrate complex to be formed. If we double the amount of enzyme present in our activity assay, the activity should double.

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
1.   How would you assay for HMG-CoA Reductase activity? Be specific a) What is the chemical...
1.   How would you assay for HMG-CoA Reductase activity? Be specific a) What is the chemical reaction? b)   How do you quantify the reaction? c)    What kind of instrumentation is/are required to perform this enzyme assay?
You are working to characterize a newly discovered enzyme. Upon performing an enzyme kinetics assay, you...
You are working to characterize a newly discovered enzyme. Upon performing an enzyme kinetics assay, you receive the following data. Here this assay was performed by placing the purified enzyme with substrate and the formation of product was measured as a function of time. Plot this data on a Michaelis Menton style of plot. Plot this data on a Lineweaver Burk style of plot. [S] (mmol/L) Vo (µmol/min) Vo (µmol/min) [10.0 µM inhibitor] 0.000 0.000 0.000 0.25 4.66 0.646 0.5...
As an enzyme is purified, both the amount of total protien and the activity of the...
As an enzyme is purified, both the amount of total protien and the activity of the purified protien go down. Why, then does the specific activity of the purified protein go up?
You add an uncompetitive inhibitor to your enzyme assay. What will happen to Km' and Vmax...
You add an uncompetitive inhibitor to your enzyme assay. What will happen to Km' and Vmax ',   relative to Km and Vmax? Choose all correct answers. Group of answer choices Vmax' is higher Vmax' is the same Km' is higher Vmax' is lower Km' is lower Km' is the same
What is the role of p-Nitrophenol in enzyme assay and how do you measure it?
What is the role of p-Nitrophenol in enzyme assay and how do you measure it?
If you perform a kirby baker assay and there is a zone of inhibition present after...
If you perform a kirby baker assay and there is a zone of inhibition present after incubation, does that necessarily mean the bacteria is susceptible to the antibiotic? why or why not? Discuss the role of standardized interpretive charts.
You are studying an enzyme in mice whose activity can be easily measured by taking blood...
You are studying an enzyme in mice whose activity can be easily measured by taking blood samples and doing an assay that measures the product of the enzyme. You are not sure on what chromosome the gene for this enzyme is located. The following enzyme activities are measured in one set of crosses: Enzyme Activity Fathers 4 mg/ml Mothers 306 mg/ml Female Offspring of the Crosses 151 mg/ml All differences are statistically significant. Male offspring of the cross have not...
Which of the following are assays which detect the ACTIVITY or FUNCTION of a protein enzyme?...
Which of the following are assays which detect the ACTIVITY or FUNCTION of a protein enzyme? You may choose more than one answer. Western Blot ELISA Hormone-stimulated adenylyl cyclase activity assay to detect the production of cAMP (using ELISA to detect cAMP) Southern Blot
Calculate the enzymatic activity (μmol/min/mL) of a protein. The kinetic assay was graphed absorbance vs. time...
Calculate the enzymatic activity (μmol/min/mL) of a protein. The kinetic assay was graphed absorbance vs. time (sec). Linear regression provided the following equation: y=0.0135x+0.0072. The kinetic assay protocol requires 0.2 mL of enzyme. Total volume of assay tube is 4 mL. Molar absorptivity (ε) = 5300 M-1 cm-1; path length = 1 cm.
Factor VIII Assay Th is is a blood test that measures the activity of factor VIII....
Factor VIII Assay Th is is a blood test that measures the activity of factor VIII. Factor VIII or factor 8 is a large protein that is important to the clotting cascade. It accelerates the activation of factor X. Factor VIII is not an enzyme, but it plays a large role in the activation of factor X. Th e factor VIII assay measures the percentage of factor VIII present in the blood. Results are represented as a percentage of factor...