Login

|
|
Enzyme Kinetics - TurnoverModerator: BioTeam
3 posts • Page 1 of 1
Enzyme Kinetics - TurnoverHi!
I am having a few problems calculating some required enzyme kinetic values. I've investigated the activity over 3 minutes of alcohol dehydrogenase at varying [S]. I used a spectrophotometer for this. From each of those graphs i've calculated the gradient (A/min) and converted this using the beer-lambert law and the reaction volume to give me velocity in "moles of product formed/min". I used this to then plot a lineweaver burke plot to get Vmax and Km values. One of the questions asks me to calculate the Kcat value. This is where i'm stuck. I have the following data at hand: Vmax = 2.442 x 10E-2 μmoles/min Amount of enzyme used each time = 0.05mL Concentration of supplied enzyme = 4μg/mL Molecular Weight of Enzyme = 150,000 Mr The enzyme however exists as a homotetramer, and has 4 identical active sites. I know I need to take that into consideration but i'm generally confused. Could someone talk me through step by step please? - TJC
3 posts • Page 1 of 1
Who is onlineUsers browsing this forum: No registered users and 0 guests |
© Biology-Online.org. All Rights Reserved. Register | Login | About Us | Contact Us | Link to Us | Disclaimer & Privacy