In general inhibitors are the substance which binds to enzyme and decreases its activity and hence decreases the rate of reaction.
7e.inhibitor B is a poor inhibitor of enzyme X
7f. B is a poor inhibitor as addition of this do not decreased the rate of forward reaction. Rate of reaction is same in the absence of inhibitor and in presence of inhibitor B.
7g. B is a competitive inhibitor.
7h. In case of a competitive inhibitor, the inhibitor remains in competition with the substrate for the active site of the enzyme, at low substrate concentration it reduces the rate of reaction. But in case of high concentration of substrate the inhibitor can be neglected, so the same Vmax and hence same reaction rate as the reaction without inhibitor can be obtained. This is not the case with Noncompetitive inhibitors as they do not bind the enzymes active site,
need help 7f and 7h Figure 3: Reaction rate produced by Enzyme X with various inhibitor...
please help!
Serine hydroxymethyltransferase is an enzyme that is found in the metabolic pathway of amino acids and catalyzes the versible conversion of L-serine to L-glycine. Answer the following questions based upon the information given about this enzyme. (28 pts) a) Draw the expected reaction of starting material and product for this reaction at physiological conditions. (6 pts) serine hydranymetiltrany erase THE NN-methylene THE glycine H2O b) A kinetic analysis of the enzyme with substrate (THF) and an unknown (to...
You are still interested in the enzyme happyase, which catalyzes the following reaction: HAPPY = SAD Previously, you determined that kcat = 400 s and Km = 10 M for your sample of happyase. Further research shows that this happyase sample was actually contaminated with a reversible inhibitor called ANGER. When ANGER is fully removed from the happyase preparation and [Eltotalis 4 nM, the measured Vmax is increased to 4.8 umes-1 and the measured Km is now 15 MM. Use...
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need help with this lab report effects of temperture/ enzyme
concetration/ and pH on enzyme activity
those are the experemint paper and results
Exercise 5: Factors Effecting Enzyme Activity A. Testing the Effect of Temperature on Enzyme Activity The purpose of this exercise is to determine the effect of temperature on enzyme activity Materials Large plastic bin Reaction chamber with rubber stopper and tube to bom 50 mL graduated cylinder beliet o bs Filter paper mot o r.com Liver...
3. Use the below tables to complete lab calculations on the worksheet on pages 2-6 of this document. You will submit the worksheet via dropbox on Canvas by you assigned lab time the week of March 30th through April 3rd. A document with sample calculations of different concentrations is provided to you on canvas. Enzyme Kinetics Lab Buffer volume (mL) Enzyme Volume (ml) Substrate Volume (ml) TOTAL VOLUME (mL) 0.04 0.5 1.5 0.04 0.25 1.5 0.04 0.1 1.5 0.04 0.05...
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...
1. According to the paper, what does lactate dehydrogenase
(LDH) do and what does it allow to happen within the myofiber? (5
points)
2. According to the paper, what is the major disadvantage of
relying on glycolysis during high-intensity exercise? (5
points)
3. Using Figure 1 in the paper, briefly describe the different
sources of ATP production at 50% versus 90% AND explain whether you
believe this depiction of ATP production applies to a Type IIX
myofiber in a human....